Home     Publications     Links     People     Pictures     Division     Genetics     Graduate Program     DBBS    Teaching    Contact   

BOWCOCK LABORATORY

Publications

  1. Feng BJ, Sun LD, Soltani-Arabshahi R, Bowcock AM, Nair RP, Stuart P, Elder JT, Schrodi SJ, Begovich AB, Abecasis GR, Zhang XJ, Callis-Duffin KP, Krueger GG, Goldgar DE. Multiple Loci within the major histocompatibility complex confer risk of psoriasis. PLoS Genet. 2009 Aug;5(8):e1000606. Epub 2009 Aug 14. PubMed PMID: 19680446; PubMed Central PMCID: PMC2718700.
  2. Council ML, Gardner JM, Helms C, Liu Y, Cornelius LA, Bowcock AM. Contribution of genetic factors for melanoma susceptibility in sporadic US melanoma patients. Exp Dermatol. 2009 May;18(5):485-7. Epub 2009 Mar 6. PubMed PMID: 19320745.
  3. Nair RP, Ding J, Duffin KC, Helms C, Voorhees JJ, Krueger GG, Bowcock AM, Abecasis GR, Elder JT. Psoriasis bench to bedside: genetics meets immunology. Arch Dermatol. 2009 Apr;145(4):462-4. PubMed PMID: 19380669.
  4. de Cid R, Riveira-Munoz E, Zeeuwen PL, Robarge J, Liao W, Dannhauser EN, Giardina E, Stuart PE, Nair R, Helms C, Escaramís G, Ballana E, Martín-Ezquerra G, den Heijer M, Kamsteeg M, Joosten I, Eichler EE, Lázaro C, Pujol RM, Armengol L, Abecasis G, Elder JT, Novelli G, Armour JA, Kwok PY, Bowcock A, Schalkwijk J, Estivill X. Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis. Nat Genet. 2009 Feb;41(2):211-5. Epub 2009 Jan 25. PubMed PMID: 19169253.
  5. Li Y, Liao W, Chang M, Schrodi SJ, Bui N, Catanese JJ, Poon A, Matsunami N, Callis-Duffin KP, Leppert MF, Bowcock AM, Kwok PY, Krueger GG, Begovich AB. Further genetic evidence for three psoriasis-risk genes: ADAM33, CDKAL1, and PTPN22. J Invest Dermatol. 2009 Mar;129(3):629-34. Epub 2008 Oct 16. PubMed PMID: 18923449.
  6. Blauvelt A, Bickenbach JR, Kulesz-Martin MF, Bowcock AM. Montagna symposium 2008: the biologic basis of psoriasis. J Invest Dermatol. 2009 Feb;129(2):259-60. PubMed PMID: 19148212.
  7. Nograles KE, Brasington RD, Bowcock AM. New insights into the pathogenesis and genetics of psoriatic arthritis. Nat Clin Pract Rheumatol. 2009 Feb;5(2):83-91. Review. PubMed PMID: 19182814.
  8. Nair RP, Duffin KC, Helms C, Ding J, Stuart PE, Goldgar D, Gudjonsson JE, Li Y, Tejasvi T, Feng BJ, Ruether A, Schreiber S, Weichenthal M, Gladman D, Rahman P, Schrodi SJ, Prahalad S, Guthery SL, Fischer J, Liao W, Kwok PY, Menter A, Lathrop GM, Wise CA, Begovich AB, Voorhees JJ, Elder JT, Krueger GG, Bowcock AM, Abecasis GR; Collaborative Association Study of Psoriasis. Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. Nat Genet. 2009 Feb;41(2):199-204. Epub 2009 Jan 25. PubMed PMID: 19169254.
  9. Onken MD, Worley LA, Long MD, Duan S, Council ML, Bowcock AM, Harbour JW. Oncogenic mutations in GNAQ occur early in uveal melanoma. Invest Ophthalmol Vis Sci. 2008 Dec;49(12):5230-4. Epub 2008 Aug 21. PubMed PMID: 18719078; PubMed Central PMCID: PMC2634606.
  10. Gurnett CA, Alaee F, Kruse LM, Desruisseau DM, Hecht JT, Wise CA, Bowcock AM, Dobbs MB. Asymmetric lower-limb malformations in individuals with homeobox PITX1 gene mutation. Am J Hum Genet. 2008 Nov;83(5):616-22. Epub 2008 Oct 23. PubMed PMID: 18950742; PubMed Central PMCID: PMC2668044.
  11. Liu Y, Helms C, Liao W, Zaba LC, Duan S, Gardner J, Wise C, Miner A, Malloy MJ, Pullinger CR, Kane JP, Saccone S, Worthington J, Bruce I, Kwok PY, Menter A, Krueger J, Barton A, Saccone NL, Bowcock AM. A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. PLoS Genet. 2008 Mar 28;4(3):e1000041. PubMed PMID: 18369459; PubMed Central PMCID: PMC2274885.
  12. Gurnett CA, Keppel C, Bick J, Bowcock AM, Dobbs MB. Absence of HOXD10 mutations in idiopathic clubfoot and sporadic vertical talus. Clin Orthop Relat Res. 2007 Sep;462:27-31. PubMed PMID: 17417092.
  13. Bowcock AM. Genomics: guilt by association. Nature. 2007 Jun 7;447(7145):645-6. PubMed PMID: 17554292.
  14. Onken MD, Worley LA, Person E, Char DH, Bowcock AM, Harbour JW. Loss of heterozygosity of chromosome 3 detected with single nucleotide polymorphisms is superior to monosomy 3 for predicting metastasis in uveal melanoma. Clin Cancer Res. 2007 May 15;13(10):2923-7. PubMed PMID: 17504992.
  15. Human Genome Structural Variation Working Group, Eichler EE, Nickerson DA, Altshuler D, Bowcock AM, Brooks LD, Carter NP, Church DM, Felsenfeld A, Guyer M, Lee C, Lupski JR, Mullikin JC, Pritchard JK, Sebat J, Sherry ST, Smith D, Valle D, Waterston RH. Completing the map of human genetic variation. Nature. 2007 May 10;447(7141):161-5. PubMed PMID: 17495918; PubMed Central PMCID: PMC2685471.
  16. Gao X, Gordon D, Zhang D, Browne R, Helms C, Gillum J, Weber S, Devroy S, Swaney S, Dobbs M, Morcuende J, Sheffield V, Lovett M, Bowcock A, Herring J, Wise C. CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis. Am J Hum Genet. 2007 May;80(5):957-65. Epub 2007 Mar 12. PubMed PMID: 17436250; PubMed Central PMCID: PMC1852746.
  17. Lowes MA, Bowcock AM, Krueger JG. Pathogenesis and therapy of psoriasis. Nature. 2007 Feb 22;445(7130):866-73. Review. PubMed PMID: 17314973.
  18. Gurnett CA, Bowcock AM, Dietz FR, Morcuende JA, Murray JC, Dobbs MB. Two novel point mutations in the long-range SHH enhancer in three families with triphalangeal thumb and preaxial polydactyly. Am J Med Genet A. 2007 Jan 1;143(1):27-32. PubMed PMID: 17152067.
  19. Liu Y, Krueger JG, Bowcock AM. Psoriasis: genetic associations and immune system changes. Genes Immun. 2007 Jan;8(1):1-12. Epub 2006 Nov 9. Review. PubMed PMID: 17093502.
  20. Gurnett CA, Dobbs MB, Keppel CR, Pincus ER, Jansen LA, Bowcock AM. Additional evidence of a locus for complex febrile and afebrile seizures on chromosome 12q22-23.3. Neurogenetics. 2007 Jan;8(1):61-3. Epub 2006 Sep 14. PubMed PMID: 16972079.
  21. Gurnett CA, Dobbs MB, Nordsieck EJ, Keppel C, Goldfarb CA, Morcuende JA, Bowcock AM. Evidence for an additional locus for split hand/foot malformation in chromosome region 8q21.11-q22.3. Am J Med Genet A. 2006 Aug 15;140(16):1744-8. PubMed PMID: 16838310.
  22. Haider AS, Peters SB, Kaporis H, Cardinale I, Fei J, Ott J, Blumenberg M, Bowcock AM, Krueger JG, Carucci JA. Genomic analysis defines a cancer-specific gene expression signature for human squamous cell carcinoma and distinguishes malignant hyperproliferation from benign hyperplasia. J Invest Dermatol. 2006 Apr;126(4):869-81. PubMed PMID: 16470182.
  23. Sun C, Mathur P, Dupuis J, Tizard R, Ticho B, Crowell T, Gardner H, Bowcock AM, Carulli J. Peptidoglycan recognition proteins Pglyrp3 and Pglyrp4 are encoded from the epidermal differentiation complex and are candidate genes for the Psors4 locus on chromosome 1q21. Hum Genet. 2006 Mar;119(1-2):113-25. Epub 2005 Dec 17. PubMed PMID: 16362825.
  24. Morar N, Bowcock AM, Harper JI, Cookson WO, Moffatt MF. Investigation of the chromosome 17q25 PSORS2 locus in atopic dermatitis. J Invest Dermatol. 2006 Mar;126(3):603-6. PubMed PMID: 16374479.
  25. Dobbs MB, Gurnett CA, Pierce B, Exner GU, Robarge J, Morcuende JA, Cole WG, Templeton PA, Foster B, Bowcock AM. HOXD10 M319K mutation in a family with isolated congenital vertical talus. J Orthop Res. 2006 Mar;24(3):448-53. PubMed PMID: 16450407.
  26. Helms C, Saccone NL, Cao L, Daw JA, Cao K, Hsu TM, Taillon-Miller P, Duan S, Gordon D, Pierce B, Ott J, Rice J, Fernandez-Vina MA, Kwok PY, Menter A, Bowcock AM. Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCR. Hum Genet. 2005 Dec;118(3-4):466-76. Epub 2005 Oct 19. PubMed PMID: 16235096. SUPPLEMENTAL DATA (.pdf)
  27. Gale SE, Frolov A, Han X, Bickel PE, Cao L, Bowcock A, Schaffer JE, Ory DS. A regulatory role for 1-acylglycerol-3-phosphate-O-acyltransferase 2 in adipocyte differentiation. J Biol Chem. 2006 Apr 21;281(16):11082-9. Epub 2006 Feb 22. PMID: 16495223.
  28. Dobbs MB, Gurnett CA, Robarge J, Gordon JE, Morcuende JA, Bowcock AM. Variable hand and foot abnormalities in family with congenital vertical talus and CDMP-1 gene mutation. J Orthop Res. 2005 Nov;23(6):1490-4. Epub 2005 Jul 11. PubMed PMID: 16005596.
  29. Helms C, Pelsue S, Cao L, Lamb E, Loffredo B, Taillon-Miller P, Herrin B, Burzenski LM, Gott B, Lyons BL, Keppler D, Shultz LD, Bowcock AM. The Tetratricopeptide repeat domain 7 gene is mutated in flaky skin mice: a model for psoriasis, autoimmunity, and anemia. Exp Biol Med (Maywood). 2005 Oct;230(9):659-67. PubMed PMID: 16179734.
  30. Bowcock AM, Krueger JG. Getting under the skin: the immunogenetics of psoriasis. Nat Rev Immunol. 2005 Sep;5(9):699-711. Review. Erratum in: Nat Rev Immunol. 2005 Oct;5(10):826. PubMed PMID: 16138103.
  31. Williams F, Meenagh A, Sleator C, Cook D, Fernandez-Vina M, Bowcock AM, Middleton D. Activating killer cell immunoglobulin-like receptor gene KIR2DS1 is associated with psoriatic arthritis. Hum Immunol. 2005 Jul;66(7):836-41. PubMed PMID: 16112031.
  32. Bowcock AM. The genetics of psoriasis and autoimmunity. Annu Rev Genomics Hum Genet. 2005;6:93-122. Review. PubMed PMID: 16124855.
  33. Bowcock AM. Understanding the pathogenesis of psoriasis, psoriatic arthritis, and autoimmunity via a fusion of molecular genetics and immunology. Immunol Res. 2005;32(1-3):45-56. Review. PubMed PMID: 16106058.
  34. Krueger JG, Bowcock A. Psoriasis pathophysiology: current concepts of pathogenesis. Ann Rheum Dis. 2005 Mar;64 Suppl 2:ii30-6. Review. PubMed PMID: 15708932; PubMed Central PMCID: PMC1766865.
  35. Bashiardes S, Veile R, Helms C, Mardis ER, Bowcock AM, Lovett M. Direct genomic selection. Nat Methods. 2005 Jan;2(1):63-9. PubMed PMID: 16152676.
  36. Gordon D, Haynes C, Johnnidis C, Patel SB, Bowcock AM, Ott J. A transmission disequilibrium test for general pedigrees that is robust to the presence of random genotyping errors and any number of untyped parents. Eur J Hum Genet. 2004 Sep;12(9):752-61. PubMed PMID: 15162128; PubMed Central PMCID: PMC1356564.
  37. Bashiardes S, Veile R, Allen M, Wise CA, Dobbs M, Morcuende JA, Szappanos L, Herring JA, Bowcock AM, Lovett M. SNTG1, the gene encoding gamma1-syntrophin: a candidate gene for idiopathic scoliosis. Hum Genet. 2004 Jun;115(1):81-9. Epub 2004 Apr 16. PubMed PMID: 15088139.
  38. Bowcock AM. Psoriasis genetics: the way forward. J Invest Dermatol. 2004 Jun;122(6):xv-xvii. Review. PubMed PMID: 15175054.
  39. Capon F, Helms C, Veal CD, Tillman D, Burden AD, Barker JN, Bowcock AM, Trembath RC. Genetic analysis of PSORS2 markers in a UK dataset supports the association between RAPTOR SNPs and familial psoriasis. J Med Genet. 2004 Jun;41(6):459-60. PubMed PMID: 15173233; PubMed Central PMCID: PMC1735814.
  40. Lew W, Bowcock AM, Krueger JG. Psoriasis vulgaris: cutaneous lymphoid tissue supports T-cell activation and "Type 1" inflammatory gene expression. Trends Immunol. 2004 Jun;25(6):295-305. Review. PubMed PMID: 15145319.
  41. Bowcock AM, Cookson WO. The genetics of psoriasis, psoriatic arthritis and atopic dermatitis. Hum Mol Genet. 2004 Apr 1;13 Spec No 1:R43-55. Review. PubMed PMID: 14996755.
  42. Suomela S, Cao L, Bowcock A, Saarialho-Kere U. Interferon alpha-inducible protein 27 (IFI27) is upregulated in psoriatic skin and certain epithelial cancers. J Invest Dermatol. 2004 Mar;122(3):717-21. PubMed PMID: 15086558.
  43. Helms C, Cao L, Krueger JG, Wijsman EM, Chamian F, Gordon D, Heffernan M, Daw JA, Robarge J, Ott J, Kwok PY, Menter A, Bowcock AM. A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis. Nat Genet. 2003 Dec;35(4):349-56. Epub 2003 Nov 9. PubMed PMID: 14608357.
  44. Bowcock AM, Barker JN. Genetics of psoriasis: the potential impact on new therapies. J Am Acad Dermatol. 2003 Aug;49(2 Suppl):S51-6. Review. PubMed PMID: 12894126.
  45. Haque WA, Oral EA, Dietz K, Bowcock AM, Agarwal AK, Garg A. Risk factors for diabetes in familial partial lipodystrophy, Dunnigan variety. Diabetes Care. 2003 May;26(5):1350-5. PubMed PMID: 12716787.
  46. Zhou X, Krueger JG, Kao MC, Lee E, Du F, Menter A, Wong WH, Bowcock AM. Novel mechanisms of T-cell and dendritic cell activation revealed by profiling of psoriasis on the 63,100-element oligonucleotide array. Physiol Genomics. 2003 Mar 18;13(1):69-78. PubMed PMID: 12644634. SUPPLEMENTAL DATA
  47. Speckman RA, Wright Daw JA, Helms C, Duan S, Cao L, Taillon-Miller P, Kwok PY, Menter A, Bowcock AM. Novel immunoglobulin superfamily gene cluster, mapping to a region of human chromosome 17q25, linked to psoriasis susceptibility. Hum Genet. 2003 Jan;112(1):34-41. Epub 2002 Oct 24. PubMed PMID: 12483297.
  48. Garg A, Speckman RA, Bowcock AM. Multisystem dystrophy syndrome due to novel missense mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C gene. Am J Med. 2002 May;112(7):549-55. PubMed PMID: 12015247.
  49. Agarwal AK, Arioglu E, De Almeida S, Akkoc N, Taylor SI, Bowcock AM, Barnes RI, Garg A. AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34. Nat Genet. 2002 May;31(1):21-3. Epub 2002 Apr 22. PubMed PMID: 11967537.
  50. Du F, Mahadevappa M, Warrington JA, and Bowcock AM: Gene expression changes in endometrial cancer. In Microarrays and Cancer, Eds. Warrington JA, Wong D, and Todd R. Eaton Publishing, pp 113-125 (2002).
  51. Swoboda KJ, Soong BW, McKenna C, Brunt ER, Litt M, Bale JF Jr, Ashizawa T, Bennett LB, Bowcock AM, Roach ES, Gerson D, Matsuura T, Heydemann PT, Nespeca MP, Jankovic J, Leppert M, Ptacek LJ. Paroxysmal kinesigenic dyskinesia and infantile convulsions. Clinical and linkage studies. 2000. Neurology. 2001 Dec;57(11 Suppl 4):S42-8. PubMed PMID: 11775608.
  52. Xu XL, Wu LC, Du F, Davis A, Peyton M, Tomizawa Y, Maitra A, Tomlinson G, Gazdar AF, Weissman BE, Bowcock AM, Baer R, Minna JD. Inactivation of human SRBC, located within the 11p15.5-p15.4 tumor suppressor region, in breast and lung cancers. Cancer Res. 2001 Nov 1;61(21):7943-9. PubMed PMID: 11691816.
  53. Bowcock AM, Shannon W, Du F, Duncan J, Cao K, Aftergut K, Catier J, Fernandez-Vina MA, Menter A. Insights into psoriasis and other inflammatory diseases from large-scale gene expression studies. Hum Mol Genet. 2001 Aug 15;10(17):1793-805. PubMed PMID: 11532989.
  54. Bowcock AM, Lovett M. Zeroing in on tolerance. Nat Med. 2001 Mar;7(3):279-81. PubMed PMID: 11231617.
  55. Garg A, Vinaitheerthan M, Weatherall PT, Bowcock AM. Phenotypic heterogeneity in patients with familial partial lipodystrophy (dunnigan variety) related to the site of missense mutations in lamin a/c gene. J Clin Endocrinol Metab. 2001 Jan;86(1):59-65. PubMed PMID: 11231979.
  56. Chatila TA, Blaeser F, Ho N, Lederman HM, Voulgaropoulos C, Helms C, Bowcock AM. JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome. J Clin Invest. 2000 Dec;106(12):R75-81. PubMed PMID: 11120765; PubMed Central PMCID: PMC387260.
  57. Wise CA, Barnes R, Gillum J, Herring JA, Bowcock AM, Lovett M. Localization of susceptibility to familial idiopathic scoliosis. Spine (Phila Pa 1976). 2000 Sep 15;25(18):2372-80. PubMed PMID: 10984791.
  58. Wise CA, Bennett LB, Pascual V, Gillum JD, Bowcock AM. Localization of a gene for familial recurrent arthritis. Arthritis Rheum. 2000 Sep;43(9):2041-5. Erratum in: Arthritis Rheum 2000 Nov;43(11):2618. PubMed PMID: 11014354.
  59. Swoboda KJ, Soong B, McKenna C, Brunt ER, Litt M, Bale JF Jr, Ashizawa T, Bennett LB, Bowcock AM, Roach ES, Gerson D, Matsuura T, Heydemann PT, Nespeca MP, Jankovic J, Leppert M, Ptacek LJ. Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies. Neurology. 2000 Jul 25;55(2):224-30. PubMed PMID: 10908896.
  60. Zhivotovsky LA, Bennett L, Bowcock AM, Feldman MW. Human population expansion and microsatellite variation. Mol Biol Evol. 2000 May;17(5):757-67. PubMed PMID: 10779536.
  61. Speckman RA, Garg A, Du F, Bennett L, Veile R, Arioglu E, Taylor SI, Lovett M, Bowcock AM. Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C. Am J Hum Genet. 2000 Apr;66(4):1192-8. Erratum in: Am J Hum Genet 2000 Sep;67(3):775. PubMed PMID: 10739751; PubMed Central PMCID: PMC1288186.
  62. Bennett LB, Roach ES, Bowcock AM. A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16. Neurology. 2000 Jan 11;54(1):125-30. PubMed PMID: 10636137.
  63. Garg A, Wilson R, Barnes R, Arioglu E, Zaidi Z, Gurakan F, Kocak N, O'Rahilly S, Taylor SI, Patel SB, Bowcock AM. A gene for congenital generalized lipodystrophy maps to human chromosome 9q34. J Clin Endocrinol Metab. 1999 Sep;84(9):3390-4. PubMed PMID: 10487716.
  64. Moran JL, Johnston SH, Rauskolb C, Bhalerao J, Bowcock AM, Vogt TF. Genomic structure, mapping, and expression analysis of the mammalian Lunatic, Manic, and Radical fringe genes. Mamm Genome. 1999 Jun;10(6):535-41. PubMed PMID: 10341080.
  65. Queimado L, Lopes C, Du F, Martins C, Fonseca I, Bowcock AM, Soares J, Lovett M. In vitro transformation of cell lines from human salivary gland tumors. Int J Cancer. 1999 May 31;81(5):793-8. PubMed PMID: 10328235.
  66. Queimado L, Lopes C, Du F, Martins C, Bowcock AM, Soares J, Lovett M. Pleomorphic adenoma gene 1 is expressed in cultured benign and malignant salivary gland tumor cells. Lab Invest. 1999 May;79(5):583-9. PubMed PMID: 10334569.
  67. Steeves TD, King DP, Zhao Y, Sangoram AM, Du F, Bowcock AM, Moore RY, Takahashi JS. Molecular cloning and characterization of the human CLOCK gene: expression in the suprachiasmatic nuclei. Genomics. 1999 Apr 15;57(2):189-200. PubMed PMID: 10198158.
  68. Bennett LB, Taurog J, and Bowcock AM: Hereditary breast cancer genes. In Breast Cancer: Molecular Genetics, Patholgenesis, and Therapeutics. A. Bowcock (Editor). Humana Press, New Jersey. Pg 199-224, 1999.
  69. Bowcock AM (Editor) Breast Cancer: Molecular Genetics, Pathogenesis, and Therapeutics in Contemporary Approaches to Cancer Series. Humana Press, Totowa, New Jersey (1999).
  70. Ayi TC, Tsan JT, Hwang LY, Bowcock AM, Baer R. Conservation of function and primary structure in the BRCA1-associated RING domain (BARD1) protein. Oncogene. 1998 Oct 22;17(16):2143-8. PubMed PMID: 9798686.
  71. Yu X, Wu LC, Bowcock AM, Aronheim A, Baer R. The C-terminal (BRCT) domains of BRCA1 interact in vivo with CtIP, a protein implicated in the CtBP pathway of transcriptional repression. J Biol Chem. 1998 Sep 25;273(39):25388-92. PubMed PMID: 9738006.
  72. Peters JM, Barnes R, Bennett L, Gitomer WM, Bowcock AM, Garg A. Localization of the gene for familial partial lipodystrophy (Dunnigan variety) to chromosome 1q21-22. Nat Genet. 1998 Mar;18(3):292-5. PubMed PMID: 9500556.
  73. Thai TH, Du F, Tsan JT, Jin Y, Phung A, Spillman MA, Massa HF, Muller CY, Ashfaq R, Mathis JM, Miller DS, Trask BJ, Baer R, Bowcock AM. Mutations in the BRCA1-associated RING domain (BARD1) gene in primary breast, ovarian and uterine cancers. Hum Mol Genet. 1998 Feb;7(2):195-202. PubMed PMID: 9425226.
  74. Bennett LB, Shriver MD, Bowcock AM. Markers and methods for reconstructing modern human history. DNA Seq. 1998;8(5):329-41. PubMed PMID: 10993603.
  75. Bhalerao J, Bowcock AM. The genetics of psoriasis: a complex disorder of the skin and immune system. Hum Mol Genet. 1998;7(10):1537-45. Review. PubMed PMID: 9735374.
  76. Bhalerao J, Silverman A, Menter A, and Bowcock AM: Genes in Psoriasis. In Psoriasis. Edited by Henry H. Roenigk, Jr. and Howard I. Maibach. Third Edition pp. 177-188 (1998).
  77. Bergstein I, Eisenberg LM, Bhalerao J, Jenkins NA, Copeland NG, Osborne MP, Bowcock AM, Brown AM. Isolation of two novel WNT genes, WNT14 and WNT15, one of which (WNT15) is closely linked to WNT3 on human chromosome 17q21. Genomics. 1997 Dec 15;46(3):450-8. PubMed PMID: 9441749.
  78. Jin Y, Xu XL, Yang MC, Wei F, Ayi TC, Bowcock AM, Baer R. Cell cycle-dependent colocalization of BARD1 and BRCA1 proteins in discrete nuclear domains. Proc Natl Acad Sci U S A. 1997 Oct 28;94(22):12075-80. PubMed PMID: 9342365; PubMed Central PMCID: PMC23707.
  79. Barcellos LF, Klitz W, Field LL, Tobias R, Bowcock AM, Wilson R, Nelson MP, Nagatomi J, Thomson G. Association mapping of disease loci, by use of a pooled DNA genomic screen. Am J Hum Genet. 1997 Sep;61(3):734-47. PubMed PMID: 9326338; PubMed Central PMCID: PMC1715937.
  80. Hoffman SM, Lai KS, Tomfohrde J, Bowcock A, Gordon LA, Mohrenweiser HW. JAK3 maps to human chromosome 19p12 within a cluster of proto-oncogenes and transcription factors. Genomics. 1997 Jul 1;43(1):109-11. PubMed PMID: 9226382.
  81. Krainer M, Silva-Arrieta S, FitzGerald MG, Shimada A, Ishioka C, Kanamaru R, MacDonald DJ, Unsal H, Finkelstein DM, Bowcock A, Isselbacher KJ, Haber DA. Differential contributions of BRCA1 and BRCA2 to early-onset breast cancer. N Engl J Med. 1997 May 15;336(20):1416-21. PubMed PMID: 9145678.
  82. Kirkpatrick H, Waber P, Hoa-Thai T, Barnes R, Osborne-Lawrence S, Truelson J, Nisen P, Bowcock A. Infrequency of BRCA2 alterations in head and neck squamous cell carcinoma. Oncogene. 1997 May 8;14(18):2189-93. PubMed PMID: 9174054.
  83. Bowcock AM: Breast cancer genes. The Breast Journal. (Supplement) 3:1-6 (1997).
  84. Wu LC, Wang ZW, Tsan JT, Spillman MA, Phung A, Xu XL, Yang MC, Hwang LY, Bowcock AM, Baer R. Identification of a RING protein that can interact in vivo with the BRCA1 gene product. Nat Genet. 1996 Dec;14(4):430-40. PubMed PMID: 8944023.
  85. Spillman MA, Bowcock AM. BRCA1 and BRCA2 mRNA levels are coordinately elevated in human breast cancer cells in response to estrogen. Oncogene. 1996 Oct 17;13(8):1639-45. PubMed PMID: 8895509.
  86. Abel KJ, Brody LC, Valdes JM, Erdos MR, McKinley DR, Castilla LH, Merajver SD, Couch FJ, Friedman LS, Ostermeyer EA, Lynch ED, King MC, Welcsh PL, Osborne-Lawrence S, Spillman M, Bowcock AM, Collins FS, Weber BL. Characterization of EZH1, a human homolog of Drosophila Enhancer of zeste near BRCA1. Genomics. 1996 Oct 15;37(2):161-71. PubMed PMID: 8921387.
  87. Hammani K, Blakis A, Morsette D, Bowcock AM, Schmutte C, Henriet P, DeClerck YA. Structure and characterization of the human tissue inhibitor of metalloproteinases-2 gene. J Biol Chem. 1996 Oct 11;271(41):25498-505. PubMed PMID: 8810321.
  88. Fischer SG, Cayanis E, de Fatima Bonaldo M, Bowcock AM, Deaven LL, Edelman IS, Gallardo T, Kalachikov S, Lawton L, Longmire JL, Lovett M, Osborne-Lawrence S, Rothstein R, Russo JJ, Soares MB, Sunjevaric I, Venkatraj VS, Warburton D, Zhang P, Efstratiadis A. A high-resolution annotated physical map of the human chromosome 13q12-13 region containing the breast cancer susceptibility locus BRCA2. Proc Natl Acad Sci U S A. 1996 Jan 23;93(2):690-4. PubMed PMID: 8570617; PubMed Central PMCID: PMC40114.
  89. Bergstein I, Schultz R, Osborne MP, Welcsh PL, Bowcock AM, Brown AM. Investigation of the possible role of WNT genes in human breast cancer. Ann N Y Acad Sci. 1995 Sep 30;768:257. PubMed PMID: 8526360.
  90. Bowcock AM. Genetic locus for psoriasis identified. Ann Med. 1995 Apr;27(2):183-6. Review. PubMed PMID: 7632411.
  91. Osborne-Lawrence S, Welcsh PL, Spillman M, Chandrasekharappa SC, Gallardo TD, Lovett M, Bowcock AM. Direct selection of expressed sequences within a 1-Mb region flanking BRCA1 on human chromosome 17q21. Genomics. 1995 Jan 1;25(1):248-55. PubMed PMID: 7774925.
  92. Bowcock AM, Chipperfield M, Ceverha P, Yetman E, and Phung A: Report of the DNA committee. In Human Gene Mapping (a compendium), The Johns Hopkins University Press, Baltimore and London, pp. 1454-1768 (1995).
  93. Couch FJ, Castilla LH, Xu J, Abel KJ, Welcsh P, King SE, Wong L, Ho PP, Merajver S, Brody LC, Yin GY, Hayes ST, Gieser LM, Flejter WL, Glover TW, Friedman LS, Lynch ED, Meza JE, King, M-C, Law DJ, Deaven L, Bowcock AM, Collins FS, Weber BL, and Chandrasekharappa SC: A YAC-, P1-, and Cosmid-Based Physical Map of the BRCA1 Region on Chromosome 17q21. Genomics 25:264-273 (1995). PMID: 7774927
  94. Orth K, Hung J, Gazdar A, Mathis M, Bowcock A, Sambrook J. Ovarian tumors display persistent microsatellite instability caused by mutation in the mismatch repair gene hMSH-2. Cold Spring Harb Symp Quant Biol. 1994;59:349-56. PubMed PMID: 7587087.
  95. Chandrasekharappa SC, Friedman L, King SE, Lee YH, Welsch P, Bowcock AM, Weber BL, King MC, Collins FS. The gene for pancreatic polypeptide (PPY) and the anonymous marker D17S78 are within 45 kb of each other on chromosome 17q21. Genomics. 1994 May 15;21(2):458-60. PubMed PMID: 8088848.
  96. Bowcock AM, Ruiz-Linares A, Tomfohrde J, Minch E, Kidd JR, Cavalli-Sforza LL. High resolution of human evolutionary trees with polymorphic microsatellites. Nature. 1994 Mar 31;368(6470):455-7. PubMed PMID: 7510853.
  97. Bowcock AM, Tomfohrde J, Weissenbach J, Bonne-Tamir B, St George-Hyslop P, Giagheddu M, Cavalli-Sforza LL, Farrer LA. Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellites. Am J Hum Genet. 1994 Jan;54(1):79-87. PubMed PMID: 8279473; PubMed Central PMCID: PMC1918061.
  98. Bowcock AM: (Chair) Statement of the American Society of Human Genetics on Genetic Testing for Breast and Ovarian Cancer Predisposition. Am. J. Hum. Genet. 55:i-iv (1994). PMID: 7977337
  99. Tomfohrde J, Silverman A, Barnes R, Fernandez-Vina MA, Young M, Lory D, Morris L, Wuepper KD, Stastny P, Menter A, and Bowcock AM: Gene for familial psoriasis susceptibility mapped to the distal end of human chromosome 17q. Science 264:1141-1145 (1994). PMID: 8178173
  100. Silverman AK, Menter A, Nemunaitis JJ, and Bowcock AM: Mapping Genes for Psoriasis. Review of a Unique Cooperative Undertaking by the Baylor Psoriasis Center, The University of Texas Southwestern Medical Center at Dallas, and the National Psoriasis Tissue Bank, BUMC Proceedings 7:13-20 (1994).
  101. Levedakou EN, He M, Baptist EW, Craven RN, Cance WG, Welcsh PL, Simmons A, Naylor SL, Leach RJ, Lewis TB, Bowcock AM, and Liu E: Two novel human serine/threonine kinases with homology to the cell cycle regulating Xenopus MO15, and NIMA kinases: cloning and characterization of their expression pattern. Oncogene 9:1977-1988 (1994). PMID: 8208544
  102. Chandrasekharappa SC, King SE, Freedman ML, Hayes ST, Bowcock AM, Collins FS. The CA repeat marker D17S791 is located within 40 kb of the WNT3 gene on chromosome 17q. Genomics. 1993 Dec;18(3):728-9. PubMed PMID: 8307586.
  103. Washington SS, Bowcock AM, Gerken S, Matsunami N, Lesh D, Osborne-Lawrence SL, Cowell J, Ledbetter DH, White RL, Chakravarti A. A somatic cell hybrid map of human chromosome 13. Genomics. 1993 Dec;18(3):486-95. PubMed PMID: 8307557.
  104. Beckmann JS, Tomfohrde J, Barnes RI, Williams M, Broux O, Richard I, Weissenbach J, Bowcock AM. A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites. Hum Mol Genet. 1993 Dec;2(12):2019-30. PubMed PMID: 7906587.
  105. Bowcock AM. Molecular cloning of BRCA1: a gene for early onset familial breast and ovarian cancer. Breast Cancer Res Treat. 1993 Nov;28(2):121-35. Review. PubMed PMID: 8173065.
  106. White A, Tomfohrde J, Stewart E, Barnes R, Le Paslier D, Weissenbach J, Cavalli-Sforza L, Farrer L, Bowcock A. A 4.5-megabase yeast artificial chromosome contig from human chromosome 13q14.3 ordering 9 polymorphic microsatellites (22 sequence-tagged sites) tightly linked to the Wilson disease locus. Proc Natl Acad Sci U S A. 1993 Nov 1;90(21):10105-9. PubMed PMID: 8234264; PubMed Central PMCID: PMC47722.
  107. Anderson LA, Friedman L, Osborne-Lawrence S, Lynch E, Weissenbach J, Bowcock A, King MC. High-density genetic map of the BRCA1 region of chromosome 17q12-q21. Genomics. 1993 Sep;17(3):618-23. PubMed PMID: 8244378.
  108. Thierfelder L, MacRae C, Watkins H, Tomfohrde J, Williams M, McKenna W, Bohm K, Noeske G, Schlepper M, Bowcock A, et al. A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2. Proc Natl Acad Sci U S A. 1993 Jul 1;90(13):6270-4. PubMed PMID: 8327508; PubMed Central PMCID: PMC46910.
  109. Bowcock A, Osborne-Lawrence S, Barnes R, Chakravarti A, Washington S, Dunn C. Microsatellite polymorphism linkage map of human chromosome 13q. Genomics. 1993 Feb;15(2):376-86. PubMed PMID: 8095487.
  110. Stewart EA, White A, Tomfohrde J, Osborne-Lawrence S, Prestridge L, Bonne-Tamir B, Scheinberg IH, St. George-Hyslop P, Giagheddu M, Kim JW, Lo WH-y, Ivanova-Smolenskaya I, Limborska S, Cavalli-Sforza LL, Farrer LA, and Bowcock AM: Polymorphic Microsatellites and Wilson disease (WD). Am. J. Hum. Genet. 53:864-873 (1993). PMID: 8213814
  111. Bowcock A. Report of the First International Workshop on Human Chromosome 13 Mapping. Dallas, Texas, September 21-22, 1992. Cytogenet Cell Genet. 1993;62(2-3):89-107. PubMed PMID: 8094043.
  112. Bowcock AM, Gerken SC, Barnes RI, Shiang R, Jabs EW, Warren AC, Antonarakis S, Retief AE, Vergnaud G, Leppert M, et al. The CEPH consortium linkage map of human chromosome 13. Genomics. 1993 May;16(2):486-96. PubMed PMID: 8314586.
  113. Bowcock AM, Anderson LA, Friedman LS, Black DM, Osborne-Lawrence S, Rowell SE, Hall JM, Solomon E, King MC. THRA1 and D17S183 flank an interval of < 4 cM for the breast-ovarian cancer gene (BRCA1) on chromosome 17q21. Am J Hum Genet. 1993 Apr;52(4):718-22. PubMed PMID: 8460637; PubMed Central PMCID: PMC1682071.
  114. Harris BD, Kurth JH, Barnes RI, Bowcock AM, Kurth MC. Linkage analysis of the monoamine A and B genes using newly-defined polymorphisms. Cytogenet Cell Genet. 1993;62(4):236-7. PubMed PMID: 8440143.
  115. Kurth JH, Bowcock AM, Erlich HA, Cavallisforza LL. HLA-DQa allelic frequencies detected with PCR in a variety of human populations. Gene Geogr. 1992 Dec;6(3):175-83. PubMed PMID: 1339494.
  116. Bowcock AM, Barnes RI, White RL, Kruse TA, Tsipouras P, Sarfarazi M, Jenkins T, Viljoen C, Litt M, Kramer PL, et al. The CEPH consortium linkage map of human chromosome 15q. Genomics. 1992 Dec;14(4):833-40. PubMed PMID: 1478662.
  117. Ben Othmane K, Ben Hamida M, Pericak-Vance MA, Ben Hamida C, Blel S, Carter SC, Bowcock AM, Petruhkin K, Gilliam TC, Roses AD, et al. Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q. Nat Genet. 1992 Dec;2(4):315-7. PubMed PMID: 1303286.
  118. Bowcock AM, Azuma T, Barnes RI, Wu SH, Bell GI, Taggart RT. Detection of a polymorphism within the pepsinogen C gene with PCR: construction of a linkage map around PGC from 6p11-6p21.3. Genomics. 1992 Oct;14(2):398-402. PubMed PMID: 1427855.
  119. Mountain JL, Lin AA, Bowcock AM, Cavalli-Sforza LL. Evolution of modern humans: evidence from nuclear DNA polymorphisms. Philos Trans R Soc Lond B Biol Sci. 1992 Aug 29;337(1280):159-65. PubMed PMID: 1357690.
  120. Bowcock A, Osborne-Lawrence S, Barnes R, Weiss L, Dunn G. Dinucleotide repeat polymorphism at the D1S167 locus. Hum Mol Genet. 1992 May;1(2):138. PubMed PMID: 1301153.
  121. Bowcock A, Osborne-Lawrence S, Barnes R, Weiss L, Dunn G. Dinucleotide repeat polymorphism at the D6S223 locus. Hum Mol Genet. 1992 Apr;1(1):66. PubMed PMID: 1301141.
  122. Albritton LM, Bowcock AM, Eddy RL, Morton CC, Tseng L, Farrer LA, Cavalli-Sforza LL, Shows TB, Cunningham JM. The human cationic amino acid transporter (ATRC1): physical and genetic mapping to 13q12-q14. Genomics. 1992 Mar;12(3):430-4. PubMed PMID: 1348489.
  123. Scharf SJ, Bowcock AM, McClure G, Klitz W, Yandell DW, Erlich HA. Amplification and characterization of the retinoblastoma gene VNTR by PCR. Am J Hum Genet. 1992 Feb;50(2):371-81. PubMed PMID: 1734717; PubMed Central PMCID: PMC1682449.
  124. Azuma T, Liu WG, Vander Laan DJ, Bowcock AM, Taggart RT. Human gastric cathepsin E gene. Multiple transcripts result from alternative polyadenylation of the primary transcripts of a single gene locus at 1q31-q32. J Biol Chem. 1992 Jan 25;267(3):1609-14. PubMed PMID: 1370478.
  125. Bowcock AM, Barnes RI, Weiss LE, Tomfohrde J, Dracopoli NC, Hudson T, Kruse TA, Sarfarazi M, Tsipouras P, Jenkins T, and Bergnaud G: Chromosome 15. In "A Comprehensive Genetic Linkage Map of the Human Genome" (NIH/CEPH Collaborative Mapping Group). Science 258:67-86 (1992).
  126. Bowcock AM: The Human Genome Project and Clinical Medicine. Oncology 6:71-75 (1992).
  127. NIH/CEPH Collaborative Mapping Group (includes A. Bowcock): A Comprehensive Genetic Linkage Map of the Human Genome. Science 258:67-86 (1992). PMID: 1439770
  128. Bowcock AM, Hebert JM, Mountain JL, Kidd JR, Rogers J, Kidd KK, Cavalli-Sforza LL. Study of an additional 58 DNA markers in five human populations from four continents. Gene Geogr. 1991 Dec;5(3):151-73. PubMed PMID: 1841601.
  129. Bowcock AM, Farrer LA, Hebert JM, Bale AE, Cavalli-Sforza L. A contiguous linkage map of chromosome 13q with 39 distinct loci separated on average by 5.1 centimorgans. Genomics. 1991 Nov;11(3):517-29. PubMed PMID: 1685473.
  130. Bowcock A, Cavalli-Sforza L. The study of variation in the human genome. Genomics. 1991 Oct;11(2):491-8. PubMed PMID: 1722770.
  131. Waber PG, Bowcock AM, Arencibia-Mireles O, Nisen PD. Nonrandom distribution of N-myc oncogene genotypes in neuroblastoma. J Natl Cancer Inst. 1991 Aug 7;83(15):1085-8. PubMed PMID: 1678788.
  132. Farrer LA, Bowcock AM, Hebert JM, Bonne-Tamir B, Sternlieb I, Giagheddu M, St George-Hyslop P, Frydman M, Lössner J, Demelia L, et al. Predictive testing for Wilson's disease using tightly linked and flanking DNA markers. Neurology. 1991 Jul;41(7):992-9. PubMed PMID: 2067662.
  133. Cogen PH, Daneshvar L, Bowcock AM, Metzger AK, Cavalli-Sforza LL. Loss of heterozygosity for chromosome 22 DNA sequences in human meningioma. Cancer Genet Cytogenet. 1991 Jun;53(2):271-7. PubMed PMID: 1676608.
  134. Spurr NK, Kelsell D, Rooke L, Cavalli-Sforza LL, Bowcock A, Feder J. Assignment of eight human genomic DNA sequences detecting high frequency restriction fragment length polymorphisms. Ann Hum Genet. 1991 May;55(Pt 2):141-50. PubMed PMID: 1683211.
  135. Kurth JH, Bowcock AM, Erlich HA, Nevo S, Cavalli-Sforza LL. Km typing with PCR: application to population screening. Am J Hum Genet. 1991 Mar;48(3):613-20. PubMed PMID: 1900145; PubMed Central PMCID: PMC1682986.
  136. Bowcock AM, Kidd JR, Mountain JL, Hebert JM, Carotenuto L, Kidd KK, Cavalli-Sforza LL. Drift, admixture, and selection in human evolution: a study with DNA polymorphisms. Proc Natl Acad Sci U S A. 1991 Feb 1;88(3):839-43. PubMed PMID: 1992475; PubMed Central PMCID: PMC50909.
  137. Taggart RT, Azuma T, Wu S, Bell GI, Bowcock AM. A highly informative polymorphism of the pepsinogen C gene detected by polymerase chain reaction. Adv Exp Med Biol. 1991;306:95-9. PubMed PMID: 1812765.
  138. Titenko NV, Kurth JH, Bowcock AM, Cavalli-Sforza LL. Polymerase chain reaction polymorphisms in HLA-DQ alpha and IL6 from Mongoloid and Caucasoid populations. Biomed Sci. 1991;2(2):175-9. PubMed PMID: 1772970.
  139. Bowcock AM: DNA markers as diagnostic tools. In Encyclopedia of Human Biology. (Renato Dulbecco, Ed) Vol. 3, pp. 135-150. Academic Press, La Jolla, CA. (1991).
  140. Bowcock AM, Herbert JM. An SspI RFLP at the D13S25 locus identified by the anonymous single copy probe H2-42. Nucleic Acids Res. 1990 Dec 11;18(23):7194. PubMed PMID: 1979860; PubMed Central PMCID: PMC332839.
  141. Hsieh CL, Bowcock AM, Farrer LA, Hebert JM, Huang KN, Cavalli-Sforza LL, Julius D, Francke U. The serotonin receptor subtype 2 locus HTR2 is on human chromosome 13 near genes for esterase D and retinoblastoma-1 and on mouse chromosome 14. Somat Cell Mol Genet. 1990 Nov;16(6):567-74. PubMed PMID: 1980030.
  142. Bowcock A, Sartorelli V. Polymorphism and mapping of the IGF1 gene, and absence of association with stature among African Pygmies. Hum Genet. 1990 Aug;85(3):349-54. PubMed PMID: 2394448.
  143. Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan HS, Chipperfield M, Cooper DN, Hewitt J, Lewitter F, et al. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms. Cytogenet Cell Genet. 1990;55(1-4):457-778. PubMed PMID: 2073845.
  144. Bonne-Tamir B, Frydman M, Agger MS, Bekeer R, Bowcock AM, Hebert JM, Cavalli-Sforza LL, Farrer LA. Wilson's disease in Israel: a genetic and epidemiological study. Ann Hum Genet. 1990 May;54(Pt 2):155-68. PubMed PMID: 2382969.
  145. Warren AC, Bowcock AM, Farrer LA, Antonarakis SE. An alpha satellite DNA polymorphism specific for the centromeric region of chromosome 13. Genomics. 1990 May;7(1):110-4. PubMed PMID: 1970794.
  146. Stewart EA, Craik CS, Hake L, Bowcock AM. Human carboxypeptidase A identifies a BglII RFLP and maps to 7q31-qter. Am J Hum Genet. 1990 Apr;46(4):795-800. PubMed PMID: 1969228; PubMed Central PMCID: PMC1683655.
  147. Bowcock AM, Hall JM, Hebert JM, King MC. Exclusion of the retinoblastoma gene and chromosome 13q as the site of a primary lesion for human breast cancer. Am J Hum Genet. 1990 Jan;46(1):12-7. PubMed PMID: 2294744; PubMed Central PMCID: PMC1683535.
  148. Bowcock AM, Taggart RT. Report of the committee on the genetic constitution of chromosome 13. Cytogenet Cell Genet. 1990;55(1-4):177-82. Review. PubMed PMID: 2073831.
  149. Williamson R, Bowcock AM, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper DN, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M and Maidak B: Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms. Cytogenet. Cell Genet. 55:457-778(1990). PMID: 2073845
  150. Kidd KK, Track RK, Bowcock AM, Ricciuti F, Hutchings G, and Chan HS: Human DNA restriction fragment length polymorphisms (RFLPs). In Genetic Maps 5th Ed. O'Brien SJ (ed). Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, pp 5.211-5.245 (1990).
  151. The Cystic Fibrosis Genetic Analysis Consortium. (Many authors including Bowcock AM). Worldwide survey of the _F508 mutation-report from the cystic fibrosis genetic analysis consortium. Am. J. Hum. Genet. 47:354-359 (1990). PMID: 2378364
  152. Kurth JH and Bowcock AM: Rapid screening of bacterial colonies with PCR: PCR Amplifications 5:18-19 (1990).
  153. Bowcock AM, Hebert JM. The alpha chain of human propionyl CoA carboxylase (PCCA) mapped to chromosome 13) detects an RFLP with XmnI. Nucleic Acids Res. 1989 Oct 25;17(20):8400. PubMed PMID: 2573043; PubMed Central PMCID: PMC335005.
  154. Bowcock AM, Hebert JM, Scheffer H, Penninga D, Buys CH. The anonymous probe pG50 identifying the locus D13S24 detects a two allele RFLP with SspI. Nucleic Acids Res. 1989 Oct 25;17(20):8399. PubMed PMID: 2573042; PubMed Central PMCID: PMC335004.
  155. Bowcock AM, Hebert JM, Scheffer H, Penninga D, Buys CH. The single copy probe pG24E2.4 [D13S21] reveals a Bsp1286 RFLP at 13q14.1-q14.2. Nucleic Acids Res. 1989 Oct 25;17(20):8398. PubMed PMID: 2573041; PubMed Central PMCID: PMC335003.
  156. Bowcock AM, Hebert JM. The anonymous probe pF5A identifying the locus D13S61 detects RFLPs with XmnI and BanII. Nucleic Acids Res. 1989 Oct 25;17(20):8397. PubMed PMID: 2573040; PubMed Central PMCID: PMC335002.
  157. Bowcock AM, Hebert JM. The anonymous probe pR1-4 which identifies the locus D13S59 detects a BanII RFLP. Nucleic Acids Res. 1989 Oct 25;17(20):8396. PubMed PMID: 2573039; PubMed Central PMCID: PMC335001.
  158. Stewart EA, Kopito R, Bowcock AM. A PstI polymorphism for the human erythrocyte surface protein band 3 (EPB3) demonstrates close linkage of EPB3 to the nerve growth factor receptor. Genomics. 1989 Oct;5(3):633-5. PubMed PMID: 2575590.
  159. Bowcock AM, Ray A, Erlich H, Sehgal PB. Rapid detection and sequencing of alleles in the 3' flanking region of the interleukin-6 gene. Nucleic Acids Res. 1989 Sep 12;17(17):6855-64. PubMed PMID: 2789373; PubMed Central PMCID: PMC318417.
  160. Shannon KM, Turhan AG, Chang SS, Bowcock AM, Rogers PC, Carroll WL, Cowan MJ, Glader BE, Eaves CJ, Eaves AC, et al. Familial bone marrow monosomy 7. Evidence that the predisposing locus is not on the long arm of chromosome 7. J Clin Invest. 1989 Sep;84(3):984-9. PubMed PMID: 2569483; PubMed Central PMCID: PMC329745.
  161. Bowcock AM, Hebert JM. The anonymous DNA probe p7-26 identifying the locus [D7S17], reveals an XmnI polymorphism. Nucleic Acids Res. 1989 Feb 25;17(4):1787. PubMed PMID: 2564193; PubMed Central PMCID: PMC331863.
  162. Fulton TR, Bowcock AM, Smith DR, Daneshvar L, Green P, Cavalli-Sforza LL, Donis-Keller H. A 12 megabase restriction map at the cystic fibrosis locus. Nucleic Acids Res. 1989 Jan 11;17(1):271-84. PubMed PMID: 2911467; PubMed Central PMCID: PMC331550.
  163. Bowcock AM, Ray A, Erlich HA, Sehgal PB. The molecular genetics of beta-2 interferon/interleukin-6 (IFN beta 2/IL6) alpha. Ann N Y Acad Sci. 1989;557:345-52. PubMed PMID: 2786699.
  164. Kidd KK, Bowcock AM, Schmidtke J, Track RK, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard HF, Gelernter J, et al. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms. Cytogenet Cell Genet. 1989;51(1-4):622-947. Review. PubMed PMID: 2676386.
  165. Merimee TJ, Hewlett BS, Wood W, Bowcock AM, Cavalli-Sforza LL. The growth hormone receptor gene in the African pygmy. Trans Assoc Am Physicians. 1989;102:163-9. PubMed PMID: 2576929.
  166. Smith DR, Fulton TR, Swain P, Bowcock A, Daneshvar L, Traver C, Gruenert DC, Davis R, Cavalli-Sforza LL, Donis-Keller H. Cystic fibrosis: diagnostic testing and the search for the gene. Clin Chem. 1989 Jul;35(7 Suppl):B17-20. Review. PubMed PMID: 2568193.
  167. Bowcock AM, Ray A, Erlich HA, Sehgal PB. The molecular genetics of beta-2 interferon/interleukin-6 (IFN beta 2/IL6) alpha. Ann N Y Acad Sci. 1989;557:345-52. PubMed PMID: 2786699.
  168. Bowcock AM, Farrer LA, Hebert JM, Agger M, Sternlieb I, Scheinberg IH, Buys CHCM, Scheffer H, Frydman M, Chajek-Saul T, Bonne-Tamir B, and Cavalli-Sforza LL: DNA markers at 13q14-q22 linked to Wilson's disease, in Molecular Probes, Technology and Medical Applications, Albertini A, Paoletti R, and Reisfeld R (eds), pp. 51-60 (1989).
  169. Bowcock AM, Farrer LA, Hebert JM, Agger M, Sternlieb I, Scheinberg IH, Buys CH, Scheffer H, Frydman M, Chajek-Saul T, et al. Eight closely linked loci place the Wilson disease locus within 13q14-q21. Am J Hum Genet. 1988 Nov;43(5):664-74. PubMed PMID: 3189332; PubMed Central PMCID: PMC1715529.
  170. Bowcock AM, Kidd JR, Lathrop GM, Daneshvar L, May LT, Ray A, Sehgal PB, Kidd KK, Cavalli-Sforza LL. The human "interferon-beta 2/hepatocyte stimulating factor/interleukin-6" gene: DNA polymorphism studies and localization to chromosome 7p21. Genomics. 1988 Jul;3(1):8-16. PubMed PMID: 2906047.
  171. Farrer LA, Bonne-Tamir B, Frydman M, Magazanik A, Kidd KK, Bowcock AM, Cavalli-Sforza LL. Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease. Hum Genet. 1988 Jun;79(2):109-17. PubMed PMID: 3164701.
  172. Bowcock AM, Fahnestock M, Goslin K, Shooter EM. The NGF and kallikrein genes of mouse, the African rat Mastomys natalensis and man: their distribution and mode of expression in the salivary gland. Brain Res. 1988 Apr;427(2):165-72. PubMed PMID: 3133079.
  173. Bowcock AM, Hebert JM, Wijsman E, Gadi I, Cavalli-Sforza LL, Boyd CD. High recombination between two physically close human basement membrane collagen genes at the distal end of chromosome 13q. Proc Natl Acad Sci U S A. 1988 Apr;85(8):2701-5. PubMed PMID: 2895928; PubMed Central PMCID: PMC280066.
  174. Bowcock AM, Hebert JM, Cavalli-Sforza LL. Polymorphisms revealed by random probe H2-10 [D13S26] which maps to chromosome 13q21-q22. Nucleic Acids Res. 1988 Mar 25;16(6):2745. PubMed PMID: 2896341; PubMed Central PMCID: PMC336426.
  175. Kidd KK, Bowcock AM, Pearson PL, Schmidtke J, Willard HF, Track RK, Ricciuti F. Report of the committee on human gene mapping by recombinant DNA techniques. Cytogenet Cell Genet. 1988;49(1-3):132-218. PubMed PMID: 2904880.
  176. Bowcock AM, Fulton TR, Daneshvar L, Vollrath D, Smith D, King M-C, Bowden D, Donis-Keller H, and Cavalli-Sforza LL: Long-range mapping of the cystic fibrosis gene region. In Cellular and Molecular Basis of Cystic Fibrosis, G Mastella and P Quinton (eds), San Francisco Press, pp. 65-72 (1988).
  177. Kitzis A, Chomel JC, and Haliassos A: (Many authors including Bowcock AM). Unusual segregation of cystic fibrosis alleles. Nature 336:316 (1988). PMID: 3194017
  178. Choi K, Hake LE, Bowcock AM, Roninson IB, Cavalli-Sforza LL. RFLPs associated with MDR2, a member of the human multidrug resistance gene family mapped to chromosome 7. Nucleic Acids Res. 1987 Aug 11;15(15):6305. PubMed PMID: 2888077; PubMed Central PMCID: PMC306095.
  179. Farrall M, Lathrop M, Spence JE, Bowcock A, Klinger K, Tsui LC. Further data on linkage between cystic fibrosis and 7C22 (D7S16). Am J Hum Genet. 1987 Aug;41(2):286-7. PubMed PMID: 3475980; PubMed Central PMCID: PMC1684226.
  180. Feder JN, Bowcock A, Cavalli-Sforza LL, Schimke RT. Two RFLPs for the human dihydrofolate reductase gene (DHFR). Nucleic Acids Res. 1987 Jul 24;15(14):5906. PubMed PMID: 2886981; PubMed Central PMCID: PMC306050.
  181. Bowcock AM, Farrer LA, Cavalli-Sforza LL, Hebert JM, Kidd KK, Frydman M, Bonne-Tamir B. Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13. Am J Hum Genet. 1987 Jul;41(1):27-35. PubMed PMID: 3474893; PubMed Central PMCID: PMC1684171.
  182. Bowcock AM, Bucci C, Hebert JM, Kidd JR, Kidd KK, Friedlaender JS, Cavalli-Sforza LL. Study of 47 DNA markers in five populations from four continents. Gene Geogr. 1987 Apr;1(1):47-64. PubMed PMID: 2908691.
  183. Bowcock AM, Scheffer H, Hebert JM, van den Berg JH, Buys CH. A high frequency RFLP identified by an anonymous single copy genomic clone at 13q14.1-13q14.2 [HGM8 assignment no. D13S22]. Nucleic Acids Res. 1987 Jan 12;15(1):382. PubMed PMID: 2881259; PubMed Central PMCID: PMC340435.
  184. Rosendorff J, Bowcock AM, Kuyl JM, Mendelow B, Pinto MR, Bernstein R. Localization of the human c-mos gene by in situ hybridization in two cases of acute nonlymphocytic leukemia type M2. Cancer Genet Cytogenet. 1987 Jan;24(1):137-41. PubMed PMID: 3466666.
  185. Bowcock AM, Hebert JM, Christiano AM, Wijsman E, Cavalli-Sforza LL, Boyd CD. The pro alpha 1 (IV) collagen gene is linked to the D13S3 locus at the distal end of human chromosome 13q. Cytogenet Cell Genet. 1987;45(3-4):234-6. PubMed PMID: 2891465.
  186. Bowcock AM, Farrer LA, Hebert JM, Bonne-Tamir B, Frydman M, Kidd KK, Cavalli-Sforza LL. A new human RFLP identified by 7D2 places D13S10 proximal to esterase D. Cytogenet Cell Genet. 1987;44(4):236-7. PubMed PMID: 2884079.
  187. Bowcock AM, Crandall J, Daneshvar L, Lee GM, Young B, Zunzunegui V, Craik C, Cavalli-Sforza LL, King MC. Genetic analysis of cystic fibrosis: linkage of DNA and classical markers in multiplex families. Am J Hum Genet. 1986 Dec;39(6):699-706. PubMed PMID: 3026172; PubMed Central PMCID: PMC1684114.
  188. Bowcock AM, Kavathas P, Margolskee RF, Herzenberg L, Cavalli-Sforza LL. An RFLP associated with pcDLeu2-14, a human T-cell differentiation antigen CD8 (Leu2) cDNA mapped to 2p12. Nucleic Acids Res. 1986 Oct 10;14(19):7817. PubMed PMID: 2877435; PubMed Central PMCID: PMC311807.
  189. Cavalli-Sforza LL, Kidd JR, Kidd KK, Bucci C, Bowcock AM, Hewlett BS, Freidlaender JS. DNA markers and genetic variation in the human species. Cold Spring Harb Symp Quant Biol. 1986;51 Pt 1:411-7. PubMed PMID: 2884067.
  190. Bowcock AM, Pinto MR, Bey E, Kuyl JM, Dusheiko GM, Bernstein R. The PLC/PRF/5 human hepatoma cell line. II. Chromosomal assignment of hepatitis B virus integration sites. Cancer Genet Cytogenet. 1985 Sep;18(1):19-26. PubMed PMID: 2992762.
  191. Bowcock AM, van Tonder S, Jenkins T. The haemoglobin H disease mental retardation syndrome: molecular studies on the South African case. Br J Haematol. 1984 Jan;56(1):69-78. PubMed PMID: 6704328.
  192. Finnegan DJ, Will BM, Bayev AA, Bowcock AM, and Brown L: Transposable DNA sequences in eukaryotes, in Genome Evolution, Systematics Association, Special Volume No. 20, eds, GA Dover and RB Flavel, (1982).
   Home     Publications     Links     People     Pictures     Division     Genetics     Graduate Program     DBBS    Teaching    Contact   

Washington University School of Medicine, Department of Genetics, Division of Human Genetics
Last updated Sept. 1, 2009