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Anne M. Bowcock - Publications

Affiliations: 
Biology & Biomedical Sciences (Human & Statistical Genetics) Washington University, Saint Louis, St. Louis, MO 
Area:
Genetics, Statistics
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177 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Manils J, Webb LV, Howes A, Janzen J, Boeing S, Bowcock AM, Ley SC. CARD14 signalling in keratinocytes induces TNF-dependent skin and systemic inflammation. Elife. 9. PMID 32597759 DOI: 10.7554/Elife.56720  0.348
2020 Rhead B, Shao X, Quach H, Ghai P, Barcellos LF, Bowcock AM. Global expression and CpG methylation analysis of primary endothelial cells before and after TNFa stimulation reveals gene modules enriched in inflammatory and infectious diseases and associated DMRs. Plos One. 15: e0230884. PMID 32231389 DOI: 10.1371/Journal.Pone.0230884  0.347
2019 Sundberg JP, Pratt CH, Silva KA, Kennedy VE, Qin W, Stearns TM, Frost J, Sundberg BA, Bowcock AM. Gain of function p.E138A alteration in Card14 leads to psoriasiform skin inflammation and implicates genetic modifiers in disease severity. Experimental and Molecular Pathology. 104286. PMID 31323190 DOI: 10.1016/J.Yexmp.2019.104286  0.383
2019 Bowcock AM, Anbunathan H, Verstraten R, Singh AD, Harbour JW. Integrative copy number analysis of uveal melanoma reveals novel candidate genes involved in tumorigenesis including a tumor suppressor role for PHF10/BAF45a. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. PMID 31227497 DOI: 10.1158/1078-0432.Ccr-18-3052  0.362
2018 Diquigiovanni C, Bergamini C, Evangelisti C, Isidori F, Vettori A, Tiso N, Argenton F, Costanzini A, Iommarini L, Anbunathan H, Pagotto U, Repaci A, Babbi G, Casadio R, Lenaz G, ... ... Bowcock A, et al. Mutant MYO1F alters the mitochondrial network and induces tumor proliferation in thyroid cancer. International Journal of Cancer. 143: 1706-1719. PMID 29672841 DOI: 10.1002/Ijc.31548  0.335
2018 Craiglow BG, Boyden LM, Hu R, Virtanen M, Su J, Rodriguez G, McCarthy C, Luna P, Larralde M, Humphrey S, Holland KE, Hogeling M, Hidalgo-Matlock B, Ferrari B, Fernandez-Faith E, ... ... Bowcock AM, et al. A Spectrum Including Features of Psoriasis and Pityriasis Rubra Pilaris. Journal of the American Academy of Dermatology. PMID 29477734 DOI: 10.1016/J.Jaad.2018.02.034  0.304
2018 Field MG, Durante MA, Anbunathan H, Cai LZ, Decatur CL, Bowcock AM, Kurtenbach S, Harbour JW. Punctuated evolution of canonical genomic aberrations in uveal melanoma. Nature Communications. 9: 116. PMID 29317634 DOI: 10.1038/S41467-017-02428-W  0.303
2017 Anbunathan H, Bowcock AM. The Molecular Revolution in Cutaneous Biology: The Era of Genome-Wide Association Studies and Statistical, Big Data, and Computational Topics. The Journal of Investigative Dermatology. 137: e113-e118. PMID 28411841 DOI: 10.1016/J.Jid.2016.03.047  0.371
2017 Field MG, Anbunathan H, Durante MA, Cai L, Alawa K, Decatur CL, Kurtenbach S, Bowcock A, Harbour JW. Abstract 3390: Clonal evolution in uveal melanoma Cancer Research. 77: 3390-3390. DOI: 10.1158/1538-7445.Am2017-3390  0.327
2016 Decatur CL, Ong E, Garg N, Anbunathan H, Bowcock AM, Field MG, Harbour JW. Driver Mutations in Uveal Melanoma: Associations With Gene Expression Profile and Patient Outcomes. Jama Ophthalmology. PMID 27123562 DOI: 10.1001/Jamaophthalmol.2016.0903  0.331
2016 Howes A, O'Sullivan PA, Breyer F, Ghose A, Cao L, Krappmann D, Bowcock AM, Ley SC. Psoriasis mutations disrupt CARD14 autoinhibition promoting BCL10-MALT1-dependent NF-κB activation. The Biochemical Journal. PMID 27071417 DOI: 10.1042/Bcj20160270  0.332
2015 Stuart PE, Nair RP, Tsoi LC, Tejasvi T, Das S, Kang HM, Ellinghaus E, Chandran V, Callis-Duffin K, Ike R, Li Y, Wen X, Enerbäck C, Gudjonsson JE, Kõks S, ... ... Bowcock AM, et al. Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture. American Journal of Human Genetics. PMID 26626624 DOI: 10.1016/J.Ajhg.2015.10.019  0.334
2015 Ammar M, Jordan CT, Cao L, Lim E, Bouchlaka Souissi C, Jrad A, Omrane I, Kouidhi S, Zaraa I, Anbunathan H, Mokni M, Doss N, Guttman-Yassky E, El Gaaied B, Menter A, ... Bowcock AM, et al. CARD14 alterations in Tunisian psoriasis patients and further characterization in European cohorts. The British Journal of Dermatology. PMID 26358359 DOI: 10.1111/Bjd.14158  0.542
2015 Ahn RS, Moslehi H, Martin MP, Abad-Santos M, Bowcock AM, Carrington M, Liao W. Inhibitory KIR3DL1 Alleles are Associated with Psoriasis. The British Journal of Dermatology. PMID 26286807 DOI: 10.1111/Bjd.14081  0.309
2015 Harden JL, Krueger JG, Bowcock AM. The immunogenetics of Psoriasis: A comprehensive review. Journal of Autoimmunity. 64: 66-73. PMID 26215033 DOI: 10.1016/J.Jaut.2015.07.008  0.339
2015 Yin X, Low HQ, Wang L, Li Y, Ellinghaus E, Han J, Estivill X, Sun L, Zuo X, Shen C, Zhu C, Zhang A, Sanchez F, Padyukov L, Catanese JJ, ... ... Bowcock A, et al. Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility. Nature Communications. 6: 6916. PMID 25903422 DOI: 10.1038/Ncomms7916  0.334
2015 Nititham J, Taylor KE, Gupta R, Chen H, Ahn R, Liu J, Seielstad M, Ma A, Bowcock AM, Criswell LA, Stahle M, Liao W. Meta-analysis of the TNFAIP3 region in psoriasis reveals a risk haplotype that is distinct from other autoimmune diseases. Genes and Immunity. 16: 120-6. PMID 25521225 DOI: 10.1038/Gene.2014.75  0.362
2015 Das S, Stuart PE, Ding J, Tejasvi T, Li Y, Tsoi LC, Chandran V, Fischer J, Helms C, Duffin KC, Voorhees JJ, Bowcock AM, Krueger GG, Lathrop GM, Nair RP, et al. Fine mapping of eight psoriasis susceptibility loci. European Journal of Human Genetics : Ejhg. 23: 844-53. PMID 25182136 DOI: 10.1038/Ejhg.2014.172  0.324
2014 Harden JL, Lewis SM, Pierson KC, Suárez-Fariñas M, Lentini T, Ortenzio FS, Zaba LC, Goldbach-Mansky R, Bowcock AM, Lowes MA. CARD14 expression in dermal endothelial cells in psoriasis. Plos One. 9: e111255. PMID 25369198 DOI: 10.1371/Journal.Pone.0111255  0.322
2014 Okada Y, Han B, Tsoi LC, Stuart PE, Ellinghaus E, Tejasvi T, Chandran V, Pellett F, Pollock R, Bowcock AM, Krueger GG, Weichenthal M, Voorhees JJ, Rahman P, Gregersen PK, et al. Fine mapping major histocompatibility complex associations in psoriasis and its clinical subtypes. American Journal of Human Genetics. 95: 162-72. PMID 25087609 DOI: 10.1016/J.Ajhg.2014.07.002  0.315
2014 Sagoo MS, Harbour JW, Stebbing J, Bowcock AM. Combined PKC and MEK inhibition for treating metastatic uveal melanoma. Oncogene. 33: 4722-3. PMID 24413085 DOI: 10.1038/Onc.2013.555  0.304
2013 Zeng X, Chen H, Gupta R, Paz-Altschul O, Bowcock AM, Liao W. Deletion of the activating NKG2C receptor and a functional polymorphism in its ligand HLA-E in psoriasis susceptibility. Experimental Dermatology. 22: 679-81. PMID 24079744 DOI: 10.1111/Exd.12233  0.336
2013 Matatall KA, Agapova OA, Onken MD, Worley LA, Bowcock AM, Harbour JW. BAP1 deficiency causes loss of melanocytic cell identity in uveal melanoma. Bmc Cancer. 13: 371. PMID 23915344 DOI: 10.1186/1471-2407-13-371  0.322
2013 Harbour JW, Roberson ED, Anbunathan H, Onken MD, Worley LA, Bowcock AM. Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma. Nature Genetics. 45: 133-5. PMID 23313955 DOI: 10.1038/Ng.2523  0.315
2013 Lu Y, Chen H, Nikamo P, Qi Low H, Helms C, Seielstad M, Liu J, Bowcock AM, Stahle M, Liao W. Association of cardiovascular and metabolic disease genes with psoriasis. The Journal of Investigative Dermatology. 133: 836-9. PMID 23190900 DOI: 10.1038/Jid.2012.366  0.321
2013 Xia J, Joyce CE, Bowcock AM, Zhang W. Noncanonical microRNAs and endogenous siRNAs in normal and psoriatic human skin. Human Molecular Genetics. 22: 737-48. PMID 23175445 DOI: 10.1093/Hmg/Dds481  0.706
2013 Ammar M, Bouchlaka-Souissi C, Helms CA, Zaraa I, Jordan CT, Anbunathan H, Bouhaha R, Kouidhi S, Doss N, Dhaoui R, Ben Osman A, Ben Ammar El Gaied A, Marrakchi R, Mokni M, Bowcock AM. Genome-wide linkage scan for psoriasis susceptibility loci in multiplex Tunisian families. The British Journal of Dermatology. 168: 583-7. PMID 23013406 DOI: 10.1111/Bjd.12050  0.576
2012 Tsoi LC, Spain SL, Knight J, Ellinghaus E, Stuart PE, Capon F, Ding J, Li Y, Tejasvi T, Gudjonsson JE, Kang HM, Allen MH, McManus R, Novelli G, Samuelsson L, ... ... Bowcock AM, et al. Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. Nature Genetics. 44: 1341-8. PMID 23143594 DOI: 10.1038/Ng.2467  0.374
2012 Lee HY, Huang Y, Bruneau N, Roll P, Roberson ED, Hermann M, Quinn E, Maas J, Edwards R, Ashizawa T, Baykan B, Bhatia K, Bressman S, Bruno MK, Brunt ER, ... ... Bowcock AM, et al. Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions. Cell Reports. 1: 2-12. PMID 22832103 DOI: 10.1016/J.Celrep.2011.11.001  0.311
2012 Chen H, Hayashi G, Lai OY, Dilthey A, Kuebler PJ, Wong TV, Martin MP, Fernandez Vina MA, McVean G, Wabl M, Leslie KS, Maurer T, Martin JN, Deeks SG, Carrington M, ... Bowcock AM, et al. Psoriasis patients are enriched for genetic variants that protect against HIV-1 disease. Plos Genetics. 8: e1002514. PMID 22577363 DOI: 10.1371/Journal.Pgen.1002514  0.323
2012 Jordan CT, Cao L, Roberson ED, Duan S, Helms CA, Nair RP, Duffin KC, Stuart PE, Goldgar D, Hayashi G, Olfson EH, Feng BJ, Pullinger CR, Kane JP, Wise CA, ... ... Bowcock AM, et al. Rare and common variants in CARD14, encoding an epidermal regulator of NF-kappaB, in psoriasis. American Journal of Human Genetics. 90: 796-808. PMID 22521419 DOI: 10.1016/J.Ajhg.2012.03.013  0.556
2012 Jordan CT, Cao L, Roberson ED, Pierson KC, Yang CF, Joyce CE, Ryan C, Duan S, Helms CA, Liu Y, Chen Y, McBride AA, Hwu WL, Wu JY, Chen YT, ... ... Bowcock AM, et al. PSORS2 is due to mutations in CARD14. American Journal of Human Genetics. 90: 784-95. PMID 22521418 DOI: 10.1016/J.Ajhg.2012.03.012  0.774
2012 Ellinghaus E, Stuart PE, Ellinghaus D, Nair RP, Debrus S, Raelson JV, Belouchi M, Tejasvi T, Li Y, Tsoi LC, Onken AT, Esko T, Metspalu A, Rahman P, Gladman DD, ... Bowcock AM, et al. Genome-wide meta-analysis of psoriatic arthritis identifies susceptibility locus at REL. The Journal of Investigative Dermatology. 132: 1133-40. PMID 22170493 DOI: 10.1038/Jid.2011.415  0.34
2012 Roberson ED, Liu Y, Ryan C, Joyce CE, Duan S, Cao L, Martin A, Liao W, Menter A, Bowcock AM. A subset of methylated CpG sites differentiate psoriatic from normal skin. The Journal of Investigative Dermatology. 132: 583-92. PMID 22071477 DOI: 10.1038/Jid.2011.348  0.716
2012 Landreville S, Agapova OA, Matatall KA, Kneass ZT, Onken MD, Lee RS, Bowcock AM, Harbour JW. Histone deacetylase inhibitors induce growth arrest and differentiation in uveal melanoma. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 18: 408-16. PMID 22038994 DOI: 10.1158/1078-0432.Ccr-11-0946  0.302
2012 Lee H, Huang Y, Edwards R, Hanna M, Bowcock A, Szepetowski P, Fu Y, Ptacek L. Mutations in the Novel Protein PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions (IN10-2.005) Neurology. 78: IN10-2.005-IN10-2.00. DOI: 10.1212/Wnl.78.1_Meetingabstracts.In10-2.005  0.32
2011 Joyce CE, Zhou X, Xia J, Ryan C, Thrash B, Menter A, Zhang W, Bowcock AM. Deep sequencing of small RNAs from human skin reveals major alterations in the psoriasis miRNAome. Human Molecular Genetics. 20: 4025-40. PMID 21807764 DOI: 10.1093/Hmg/Ddr331  0.696
2011 Chen H, Poon A, Yeung C, Helms C, Pons J, Bowcock AM, Kwok PY, Liao W. A genetic risk score combining ten psoriasis risk loci improves disease prediction. Plos One. 6: e19454. PMID 21559375 DOI: 10.1371/Journal.Pone.0019454  0.32
2011 Suárez-Fariñas M, Tintle SJ, Shemer A, Chiricozzi A, Nograles K, Cardinale I, Duan S, Bowcock AM, Krueger JG, Guttman-Yassky E. Nonlesional atopic dermatitis skin is characterized by broad terminal differentiation defects and variable immune abnormalities. The Journal of Allergy and Clinical Immunology. 127: 954-64.e1-4. PMID 21388663 DOI: 10.1016/J.Jaci.2010.12.1124  0.326
2011 Riveira-Munoz E, He SM, Escaramís G, Stuart PE, Hüffmeier U, Lee C, Kirby B, Oka A, Giardina E, Liao W, Bergboer J, Kainu K, de Cid R, Munkhbat B, Zeeuwen PL, ... ... Bowcock A, et al. Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6. The Journal of Investigative Dermatology. 131: 1105-9. PMID 21107349 DOI: 10.1038/Jid.2010.350  0.349
2010 Harbour JW, Onken MD, Roberson ED, Duan S, Cao L, Worley LA, Council ML, Matatall KA, Helms C, Bowcock AM. Frequent mutation of BAP1 in metastasizing uveal melanomas. Science (New York, N.Y.). 330: 1410-3. PMID 21051595 DOI: 10.1126/Science.1194472  0.344
2010 Sun LD, Cheng H, Wang ZX, Zhang AP, Wang PG, Xu JH, Zhu QX, Zhou HS, Ellinghaus E, Zhang FR, Pu XM, Yang XQ, Zhang JZ, Xu AE, Wu RN, ... ... Bowcock AM, et al. Association analyses identify six new psoriasis susceptibility loci in the Chinese population. Nature Genetics. 42: 1005-9. PMID 20953187 DOI: 10.1038/Ng.690  0.338
2010 Roberson ED, Bowcock AM. Psoriasis genetics: breaking the barrier. Trends in Genetics : Tig. 26: 415-23. PMID 20692714 DOI: 10.1016/J.Tig.2010.06.006  0.351
2010 Li Y, Liao W, Cargill M, Chang M, Matsunami N, Feng BJ, Poon A, Callis-Duffin KP, Catanese JJ, Bowcock AM, Leppert MF, Kwok PY, Krueger GG, Begovich AB. Carriers of rare missense variants in IFIH1 are protected from psoriasis. The Journal of Investigative Dermatology. 130: 2768-72. PMID 20668468 DOI: 10.1038/Jid.2010.214  0.357
2010 Bowcock AM. Genome-wide association studies and infectious disease. Critical Reviews in Immunology. 30: 305-9. PMID 20370638 DOI: 10.1615/Critrevimmunol.V30.I3.80  0.33
2009 Guttman-Yassky E, Suárez-Fariñas M, Chiricozzi A, Nograles KE, Shemer A, Fuentes-Duculan J, Cardinale I, Lin P, Bergman R, Bowcock AM, Krueger JG. Broad defects in epidermal cornification in atopic dermatitis identified through genomic analysis. The Journal of Allergy and Clinical Immunology. 124: 1235-1244.e58. PMID 20004782 DOI: 10.1016/J.Jaci.2009.09.031  0.321
2009 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 Genetics. 5: e1000606. PMID 19680446 DOI: 10.1371/Journal.Pgen.1000606  0.327
2009 Council ML, Gardner JM, Helms C, Liu Y, Cornelius LA, Bowcock AM. Contribution of genetic factors for melanoma susceptibility in sporadic US melanoma patients. Experimental Dermatology. 18: 485-7. PMID 19320745 DOI: 10.1111/J.1600-0625.2008.00807.X  0.365
2009 Nograles KE, Brasington RD, Bowcock AM. New insights into the pathogenesis and genetics of psoriatic arthritis. Nature Clinical Practice. Rheumatology. 5: 83-91. PMID 19182814 DOI: 10.1038/Ncprheum0987  0.311
2009 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, ... ... Bowcock AM, et al. Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. Nature Genetics. 41: 199-204. PMID 19169254 DOI: 10.1038/Ng.311  0.359
2009 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, ... ... Bowcock A, et al. Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis. Nature Genetics. 41: 211-5. PMID 19169253 DOI: 10.1038/Ng.313  0.38
2009 Gurnett CA, Alaee F, Bowcock A, Kruse L, Lenke LG, Bridwell KH, Kuklo T, Luhmann SJ, Dobbs MB. Genetic linkage localizes an adolescent idiopathic scoliosis and pectus excavatum gene to chromosome 18 q. Spine. 34: E94-100. PMID 19139660 DOI: 10.1097/Brs.0B013E31818B88A5  0.351
2009 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. The Journal of Investigative Dermatology. 129: 629-34. PMID 18923449 DOI: 10.1038/Jid.2008.297  0.32
2008 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. American Journal of Human Genetics. 83: 616-22. PMID 18950742 DOI: 10.1016/J.Ajhg.2008.10.004  0.4
2008 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, ... ... Bowcock AM, et al. A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. Plos Genetics. 4: e1000041. PMID 18369459 DOI: 10.1371/Journal.Pgen.1000041  0.352
2007 Bowcock AM. Genomics: guilt by association. Nature. 447: 645-6. PMID 17554292 DOI: 10.1038/447645A  0.315
2007 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. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 13: 2923-7. PMID 17504992 DOI: 10.1158/1078-0432.Ccr-06-2383  0.315
2007 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, et al. Completing the map of human genetic variation. Nature. 447: 161-5. PMID 17495918 DOI: 10.1038/447161A  0.332
2007 Gurnett CA, Keppel C, Bick J, Bowcock AM, Dobbs MB. Absence of HOXD10 mutations in idiopathic clubfoot and sporadic vertical talus. Clinical Orthopaedics and Related Research. 462: 27-31. PMID 17417092 DOI: 10.1097/Blo.0B013E31805D8649  0.403
2007 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. American Journal of Medical Genetics. Part A. 143: 27-32. PMID 17152067 DOI: 10.1002/Ajmg.A.31563  0.343
2006 Liu Y, Krueger JG, Bowcock AM. Psoriasis: genetic associations and immune system changes. Genes and Immunity. 8: 1-12. PMID 17093502 DOI: 10.1038/Sj.Gene.6364351  0.37
2006 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. American Journal of Medical Genetics. Part A. 140: 1744-8. PMID 16838310 DOI: 10.1002/Ajmg.A.31375  0.386
2006 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. Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society. 24: 448-53. PMID 16450407 DOI: 10.1002/Jor.20052  0.386
2006 Morar N, Bowcock AM, Harper JI, Cookson WO, Moffatt MF. Investigation of the chromosome 17q25 PSORS2 locus in atopic dermatitis. The Journal of Investigative Dermatology. 126: 603-6. PMID 16374479 DOI: 10.1038/Sj.Jid.5700108  0.388
2006 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. Human Genetics. 119: 113-25. PMID 16362825 DOI: 10.1007/S00439-005-0115-8  0.428
2005 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, et al. Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCR. Human Genetics. 118: 466-76. PMID 16235096 DOI: 10.1007/S00439-005-0048-2  0.358
2005 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. Experimental Biology and Medicine (Maywood, N.J.). 230: 659-67. PMID 16179734 DOI: 10.1177/153537020523000908  0.365
2005 Bowcock AM, Krueger JG. Getting under the skin: the immunogenetics of psoriasis. Nature Reviews. Immunology. 5: 699-711. PMID 16138103 DOI: 10.1038/Nri1689  0.358
2005 Bowcock AM. The genetics of psoriasis and autoimmunity. Annual Review of Genomics and Human Genetics. 6: 93-122. PMID 16124855 DOI: 10.1146/Annurev.Genom.6.080604.162324  0.378
2005 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. Human Immunology. 66: 836-41. PMID 16112031 DOI: 10.1016/J.Humimm.2005.04.005  0.345
2005 Bowcock AM. Understanding the pathogenesis of psoriasis, psoriatic arthritis, and autoimmunity via a fusion of molecular genetics and immunology. Immunologic Research. 32: 45-56. PMID 16106058 DOI: 10.1385/Ir:32:1-3:045  0.348
2005 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. Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society. 23: 1490-4. PMID 16005596 DOI: 10.1016/J.Orthres.2005.04.011  0.352
2005 Krueger JG, Bowcock A. Psoriasis pathophysiology: current concepts of pathogenesis. Annals of the Rheumatic Diseases. ii30-6. PMID 15708932 DOI: 10.1136/Ard.2004.031120  0.319
2004 Bowcock AM. Psoriasis genetics: the way forward. The Journal of Investigative Dermatology. 122: xv-xvii. PMID 15175054 DOI: 10.1111/J.0022-202X.2004.22627.X  0.384
2004 Lew W, Bowcock AM, Krueger JG. Psoriasis vulgaris: cutaneous lymphoid tissue supports T-cell activation and "Type 1" inflammatory gene expression. Trends in Immunology. 25: 295-305. PMID 15145319 DOI: 10.1016/J.It.2004.03.006  0.305
2004 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. Human Genetics. 115: 81-9. PMID 15088139 DOI: 10.1007/S00439-004-1121-Y  0.426
2004 Suomela S, Cao L, Bowcock A, Saarialho-Kere U. Interferon alpha-inducible protein 27 (IFI27) is upregulated in psoriatic skin and certain epithelial cancers. The Journal of Investigative Dermatology. 122: 717-21. PMID 15086558 DOI: 10.1111/J.0022-202X.2004.22322.X  0.305
2004 Bowcock AM, Cookson WO. The genetics of psoriasis, psoriatic arthritis and atopic dermatitis. Human Molecular Genetics. 13: R43-55. PMID 14996755 DOI: 10.1093/Hmg/Ddh094  0.426
2003 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. Nature Genetics. 35: 349-56. PMID 14608357 DOI: 10.1038/Ng1268  0.402
2003 Bowcock AM, Barker JN. Genetics of psoriasis: the potential impact on new therapies. Journal of the American Academy of Dermatology. 49: S51-6. PMID 12894126 DOI: 10.1016/S0190-9622(03)01135-6  0.368
2003 Allen M, Barker J, Bowcock A, Burden A, Capon F, Chia N, Christophers E, Daly M, Elder J, Helms C, Henseler T, Jenisch S, Menter A, Mistry R, Nair R, et al. The international psoriasis genetics study: Assessing linkage to 14 candidate susceptibility loci in a cohort of 942 affected sib pairs American Journal of Human Genetics. 73: 430-437. PMID 12851855 DOI: 10.1086/377159  0.321
2003 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. Physiological Genomics. 13: 69-78. PMID 12644634 DOI: 10.1152/Physiolgenomics.00157.2002  0.323
2003 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. Human Genetics. 112: 34-41. PMID 12483297 DOI: 10.1007/S00439-002-0851-Y  0.419
2002 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. The American Journal of Medicine. 112: 549-55. PMID 12015247 DOI: 10.1016/S0002-9343(02)01070-7  0.336
2002 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. Nature Genetics. 31: 21-3. PMID 11967537 DOI: 10.1038/Ng880  0.327
2002 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. Human Molecular Genetics. 10: 1793-805. PMID 11532989 DOI: 10.1093/Hmg/10.17.1793  0.396
2001 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. The Journal of Clinical Endocrinology and Metabolism. 86: 59-65. PMID 11231979 DOI: 10.1210/Jcem.86.1.7121  0.319
2001 Bowcock AM, Lovett M. Zeroing in on tolerance. Nature Medicine. 7: 279-81. PMID 11231617 DOI: 10.1038/85408  0.389
2000 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. The Journal of Clinical Investigation. 106: R75-81. PMID 11120765 DOI: 10.1172/Jci11679  0.322
2000 Wise CA, Bennett LB, Pascual V, Gillum JD, Bowcock AM. Localization of a gene for familial recurrent arthritis Arthritis and Rheumatism. 43: 2041-2045. PMID 11014354 DOI: 10.1002/1529-0131(200009)43:9<2041::Aid-Anr15>3.0.Co;2-G  0.387
2000 Wise CA, Barnes R, Gillum J, Herring JA, Bowcock AM, Lovett M. Localization of susceptibility to familial idiopathic scoliosis. Spine. 25: 2372-80. PMID 10984791 DOI: 10.1097/00007632-200009150-00017  0.308
2000 Swoboda KJ, Soong B, McKenna C, Brunt ER, Litt M, Bale JF, Ashizawa T, Bennett LB, Bowcock AM, Roach ES, Gerson D, Matsuura T, Heydemann PT, Nespeca MP, Jankovic J, et al. Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies. Neurology. 55: 224-30. PMID 10908896 DOI: 10.1212/Wnl.55.2.224  0.333
2000 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. American Journal of Human Genetics. 66: 1192-8. PMID 10739751 DOI: 10.1086/302836  0.366
2000 Bennett LB, Roach ES, Bowcock AM. A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16. Neurology. 54: 125-30. PMID 10636137 DOI: 10.1212/Wnl.54.1.125  0.366
1999 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. The Journal of Clinical Endocrinology and Metabolism. 84: 3390-4. PMID 10487716 DOI: 10.1210/Jcem.84.9.6103  0.379
1999 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. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 10: 535-41. PMID 10341080 DOI: 10.1007/S003359901039  0.392
1999 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. 57: 189-200. PMID 10198158 DOI: 10.1006/Geno.1998.5675  0.351
1998 Bhalerao J, Bowcock AM. The genetics of psoriasis: a complex disorder of the skin and immune system. Human Molecular Genetics. 7: 1537-45. PMID 9735374 DOI: 10.1093/Hmg/7.10.1537  0.43
1998 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. Nature Genetics. 18: 292-5. PMID 9500556 DOI: 10.1038/Ng0398-292  0.357
1998 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. 46: 450-8. PMID 9441749 DOI: 10.1006/Geno.1997.5041  0.369
1998 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. Human Molecular Genetics. 7: 195-202. PMID 9425226 DOI: 10.1093/Hmg/7.2.195  0.305
1997 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 American Journal of Human Genetics. 61: 734-747. PMID 9326338 DOI: 10.1086/515512  0.348
1997 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. 43: 109-11. PMID 9226382 DOI: 10.1006/Geno.1997.4792  0.341
1997 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. 14: 2189-93. PMID 9174054 DOI: 10.1038/Sj.Onc.1201060  0.348
1996 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, et al. Characterization of EZH1, a human homolog of Drosophila enhancer of zeste near BRCA1 Genomics. 37: 161-171. PMID 8921387 DOI: 10.1006/Geno.1996.0537  0.308
1996 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. The Journal of Biological Chemistry. 271: 25498-505. PMID 8810321 DOI: 10.1074/Jbc.271.41.25498  0.328
1996 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, et al. A high-resolution annotated physical map of the human chromosome 13q12-13 region containing the breast cancer susceptibility locus BRCA2. Proceedings of the National Academy of Sciences of the United States of America. 93: 690-4. PMID 8570617 DOI: 10.1073/Pnas.93.2.690  0.334
1996 Thomson G, Barcellos L, Klitz W, Field L, Tobias R, Bowcock A, Wilson R, Gilbert S. Association mapping with a pooled DNA genomic screen of the non-HLA genes in IDDM, RA and MS Human Immunology. 47: 152. DOI: 10.1016/0198-8859(96)85525-X  0.314
1995 Couch FJ, Castilla LH, Xu J, Abel KJ, Welcsh P, King SE, Wong L, Ho PP, Merajver S, Brody LC, Yin G, Hayes ST, Gieser LM, Flejter WL, Glover TW, ... ... Bowcock AM, et al. A YAC-, P1-, and cosmid-based physical Map of the BRCA1 region on chromosome 17q21 Genomics. 25: 264-273. PMID 7774927 DOI: 10.1016/0888-7543(95)80134-8  0.35
1995 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. 25: 248-55. PMID 7774925 DOI: 10.1016/0888-7543(95)80132-6  0.378
1995 Bowcock AM. Genetic locus for psoriasis identified. Annals of Medicine. 27: 183-6. PMID 7632411 DOI: 10.3109/07853899509031956  0.312
1994 Tomfohrde J, Silverman A, Barnes R, Fernandez-Vina MA, Young M, Lory D, Morris L, Wuepper KD, Stastny P, Menter A, Bowcock A. Gene for familial psoriasis susceptibility mapped to the distal end of human chromosome 17q Science. 264: 1141-1145. PMID 8178173 DOI: 10.1126/Science.8178173  0.421
1994 Bowcock AM. Molecular cloning of BRCA1: a gene for early onset familial breast and ovarian cancer. Breast Cancer Research and Treatment. 28: 121-35. PMID 8173065 DOI: 10.1007/Bf00666425  0.37
1994 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. 21: 458-60. PMID 8088848 DOI: 10.1006/Geno.1994.1299  0.395
1994 Orth K, Hung J, Gazdar A, Bowcock A, Mathis JM, Sambrook J. Genetic instability in human ovarian cancer cell lines. Proceedings of the National Academy of Sciences of the United States of America. 91: 9495-9. PMID 7937795 DOI: 10.1073/Pnas.91.20.9495  0.349
1994 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. Human Molecular Genetics. 2: 2019-30. PMID 7906587 DOI: 10.1093/Hmg/2.12.2019  0.347
1994 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 Harbor Symposia On Quantitative Biology. 59: 349-356. PMID 7587087 DOI: 10.1101/Sqb.1994.059.01.039  0.312
1994 Bowcock AM, Ruiz-Linares A, Tomfohrde J, Minch E, Kidd JR, Cavalli-Sforza LL. High resolution of human evolutionary trees with polymorphic microsatellites. Nature. 368: 455-7. PMID 7510853 DOI: 10.1038/368455A0  0.314
1994 Fernandez-Viña M, Tomfohrde J, Silverman A, Barnes R, Sang S, Young M, Lory D, Morris L, Wuepper K, Menter A, Bowcock A, Stastny P. HLA genes in familial psoriasis vulgaris (PV): Evidence for genetic heterogeneity Human Immunology. 40: 33. DOI: 10.1016/0198-8859(94)91725-6  0.354
1993 Harris AD, Kurth JH, Barnes RI, Bowcock AM, Kurth MC. Linkage analysis of the monoamine A and B genes using newly-defined polymorphisms Cytogenetic and Genome Research. 62: 236-237. PMID 8440143 DOI: 10.1159/000133485  0.348
1993 Thierfelder L, MacRae C, Watkins H, Tomfohrde J, Williams M, McKenna W, Bohm K, Noeske G, Schlepper M, Bowcock A. A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2. Proceedings of the National Academy of Sciences of the United States of America. 90: 6270-4. PMID 8327508 DOI: 10.1073/Pnas.90.13.6270  0.37
1993 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. 18: 728-9. PMID 8307586 DOI: 10.1016/S0888-7543(05)80386-6  0.369
1993 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. 18: 486-95. PMID 8307557 DOI: 10.1016/S0888-7543(11)80004-2  0.342
1993 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. 17: 618-23. PMID 8244378 DOI: 10.1006/Geno.1993.1381  0.372
1993 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. Proceedings of the National Academy of Sciences of the United States of America. 90: 10105-9. PMID 8234264 DOI: 10.1073/Pnas.90.21.10105  0.401
1993 Bowcock A, Osborne-Lawrence S, Barnes R, Chakravarti A, Washington S, Dunn C. Microsatellite polymorphism linkage map of human chromosome 13q. Genomics. 15: 376-86. PMID 8095487 DOI: 10.1006/Geno.1993.1071  0.365
1993 Bowcock A. Report of the First International Workshop on Human Chromosome 13 Mapping. Dallas, Texas, September 21-22, 1992. Cytogenetics and Cell Genetics. 62: 89-107. PMID 8094043 DOI: 10.1159/000133450  0.305
1993 Bowcock A, Osborne-Lawrence S, Barnes R, Weiss L, Dunn G. Dinucleotide repeat polymorphism at the D1S167 locus. Human Molecular Genetics. 1: 138. PMID 1301153 DOI: 10.1093/Hmg/1.2.138  0.32
1993 Bowcock A, Osborne-Lawrence S, Barnes R, Weiss L, Dunn G. Dinucleotide repeat polymorphism at the D6S223 locus. Human Molecular Genetics. 1: 66. PMID 1301141 DOI: 10.1093/Hmg/1.1.66  0.32
1992 Bowcock A, Cavalli-Sforza L. The study of variation in the human genome. Genomics. 11: 491-8. PMID 1722770 DOI: 10.1016/0888-7543(91)90170-J  0.32
1992 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. 11: 517-29. PMID 1685473 DOI: 10.1016/0888-7543(91)90058-M  0.351
1992 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. 14: 398-402. PMID 1427855 DOI: 10.1016/S0888-7543(05)80232-0  0.377
1992 Mountain JL, Lin AA, Bowcock AM, Cavalli-Sforza LL. Evolution of modern humans: evidence from nuclear DNA polymorphisms Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences. 337: 159-165. PMID 1357690 DOI: 10.1098/Rstb.1992.0093  0.342
1992 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. 12: 430-4. PMID 1348489 DOI: 10.1016/0888-7543(92)90431-Q  0.372
1992 Ben Othmane K, Ben Hamida M, Pericak-Vance MA, Ben Hamida C, Blel S, Carter SC, Bowcock AM, Petruhkin K, Gilliam TC, Roses AD. Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q. Nature Genetics. 2: 315-7. PMID 1303286 DOI: 10.1038/Ng1292-315  0.351
1991 Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan HS, Chipperfield M, Cooper DN, Hewitt J, Lewitter F. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms. Cytogenetics and Cell Genetics. 55: 457-778. PMID 2073845 DOI: 10.1159/000133027  0.325
1991 Farrer LA, Bowcock AM, Hebert JM, Bonné-Tamir B, Sternlieb I, Giagheddu M, St George-Hyslop P, Frydman M, Lössner J, Demelia L. Predictive testing for Wilson's disease using tightly linked and flanking DNA markers. Neurology. 41: 992-9. PMID 2067662 DOI: 10.1212/Wnl.41.7.992  0.374
1991 Bowcock AM, Kidd JR, Mountain JL, Hebert JM, Carotenuto L, Kidd KK, Luca Cavalli-Sforza L. Drift, admixture, and selection in human evolution: A study with DNA polymorphisms Proceedings of the National Academy of Sciences of the United States of America. 88: 839-843. PMID 1992475 DOI: 10.1073/Pnas.88.3.839  0.329
1991 Taggart RT, Azuma T, Wu S, Bell GI, Bowcock AM. A highly informative polymorphism of the pepsinogen C gene detected by polymerase chain reaction Advances in Experimental Medicine and Biology. 306: 95-99. PMID 1812765 DOI: 10.1007/978-1-4684-6012-4_10  0.398
1991 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. Annals of Human Genetics. 55: 141-50. PMID 1683211 DOI: 10.1111/J.1469-1809.1991.Tb00407.X  0.32
1991 Waber PG, Bowcock AM, Arencibia-Mireles O, Nisen PD. Nonrandom distribution of N-myc oncogene genotypes in neuroblastoma. Journal of the National Cancer Institute. 83: 1085-8. PMID 1678788 DOI: 10.1093/Jnci/83.15.1085  0.308
1991 Cogen PH, Daneshvar L, Bowcock AM, Metzger AK, Cavalli-Sforza LL. Loss of heterozygosity for chromosome 22 DNA sequences in human meningioma. Cancer Genetics and Cytogenetics. 53: 271-7. PMID 1676608 DOI: 10.1016/0165-4608(91)90104-3  0.373
1991 Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, et al. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 8 of 27) Cytogenetic and Genome Research. 58: 1400-1439. DOI: 10.1159/000317214  0.332
1991 Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, et al. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms Cytogenetic and Genome Research. 58: 1190-1832. DOI: 10.1159/000133727  0.332
1990 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. 5: 633-5. PMID 2575590 DOI: 10.1016/0888-7543(89)90034-7  0.339
1990 Bowcock A, Sartorelli V. Polymorphism and mapping of the IGF1 gene, and absence of association with stature among African Pygmies. Human Genetics. 85: 349-54. PMID 2394448 DOI: 10.1007/Bf00206760  0.362
1990 Bonné-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. Annals of Human Genetics. 54: 155-68. PMID 2382969 DOI: 10.1111/J.1469-1809.1990.Tb00372.X  0.353
1990 Bowcock AM, Taggart RT. Report of the committee on the genetic constitution of chromosome 13. Cytogenetics and Cell Genetics. 55: 177-82. PMID 2073831 DOI: 10.1159/000133009  0.319
1990 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. Somatic Cell and Molecular Genetics. 16: 567-74. PMID 1980030 DOI: 10.1007/Bf01233097  0.363
1990 Warren AC, Bowcock AM, Farrer LA, Antonarakis SE. An alpha satellite DNA polymorphism specific for the centromeric region of chromosome 13 Genomics. 7: 110-114. PMID 1970794 DOI: 10.1016/0888-7543(90)90525-Y  0.364
1990 Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan H, Chipperfield M, Cooper D, Hewitt J, Lewitter F, Maidak B, Quitt M, Ricciuti F, Track R, Tolley M, et al. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 13 of 14) Cytogenetic and Genome Research. 55: 757-768. DOI: 10.1159/000317054  0.325
1989 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 Research. 17: 271-84. PMID 2911467 DOI: 10.1093/Nar/17.1.271  0.339
1989 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. 3: 8-16. PMID 2906047 DOI: 10.1016/0888-7543(88)90152-8  0.378
1989 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. Cytogenetics and Cell Genetics. 49: 132-218. PMID 2904880 DOI: 10.1159/000132664  0.324
1989 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 Research. 17: 6855-64. PMID 2789373 DOI: 10.1093/Nar/17.17.6855  0.346
1989 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 Research. 17: 8399. PMID 2573042 DOI: 10.1093/Nar/17.20.8399  0.314
1989 Shannon KM, Turhan AG, Chang SS, Bowcock AM, Rogers PC, Carroll WL, Cowan MJ, Glader BE, Eaves CJ, Eaves AC. Familial bone marrow monosomy 7. Evidence that the predisposing locus is not on the long arm of chromosome 7. The Journal of Clinical Investigation. 84: 984-9. PMID 2569483 DOI: 10.1172/Jci114262  0.351
1989 Bowcock AM, Hebert JM. The anonymous DNA probe p7-26 identifying the locus [D7S17], reveals an XmnI polymorphism. Nucleic Acids Research. 17: 1787. PMID 2564193 DOI: 10.1093/Nar/17.4.1787  0.329
1989 Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 922–947 Cytogenetic and Genome Research. 51: 922-947. DOI: 10.1159/000227799  0.326
1989 Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 892–921 Cytogenetic and Genome Research. 51: 892-921. DOI: 10.1159/000227798  0.326
1989 Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 862–891 Cytogenetic and Genome Research. 51: 862-891. DOI: 10.1159/000227797  0.326
1989 Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 832–861 Cytogenetic and Genome Research. 51: 832-861. DOI: 10.1159/000227796  0.326
1989 Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 807–831 Cytogenetic and Genome Research. 51: 807-831. DOI: 10.1159/000227795  0.326
1989 Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 782–806 Cytogenetic and Genome Research. 51: 782-806. DOI: 10.1159/000227794  0.326
1989 Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 758–781 Cytogenetic and Genome Research. 51: 758-781. DOI: 10.1159/000227793  0.326
1989 Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 732–757 Cytogenetic and Genome Research. 51: 732-757. DOI: 10.1159/000227792  0.326
1989 Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 702–731 Cytogenetic and Genome Research. 51: 702-731. DOI: 10.1159/000227791  0.326
1989 Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 677–701 Cytogenetic and Genome Research. 51: 677-701. DOI: 10.1159/000227790  0.326
1989 Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 644–676 Cytogenetic and Genome Research. 51: 644-676. DOI: 10.1159/000227789  0.326
1988 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. Human Genetics. 79: 109-17. PMID 3164701 DOI: 10.1007/Bf00280547  0.343
1988 Bowcock AM, Hebert JM, Cavalli-Sforza LL. Polymorphisms revealed by random probe H2-10 [D13S26] which maps to chromosome 13q21-q22. Nucleic Acids Research. 16: 2745. PMID 2896341 DOI: 10.1093/Nar/16.6.2745  0.313
1988 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 Proceedings of the National Academy of Sciences of the United States of America. 85: 2701-2705. PMID 2895928 DOI: 10.1073/Pnas.85.8.2701  0.369
1988 Kidd K, Bowcock A, Pearson P, Schmidtke J, Willard H, Track R, Ricciuti F. Report of the committee on human gene mapping by recombinant DNA techniques (Part 3 of 6) Cytogenetic and Genome Research. 49: 162-175. DOI: 10.1159/000317005  0.324
1987 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 Genetics and Cytogenetics. 24: 137-41. PMID 3466666 DOI: 10.1016/0165-4608(87)90090-2  0.31
1987 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 Cytogenetic and Genome Research. 45: 234-236. PMID 2891465 DOI: 10.1159/000132460  0.326
1987 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 Research. 15: 6305. PMID 2888077 DOI: 10.1093/Nar/15.15.6305  0.347
1987 Feder JN, Bowcock A, Cavalli-Sforza LL, Schimke RT. Two RFLPs for the human dihydrofolate reductase gene (DHFR). Nucleic Acids Research. 15: 5906. PMID 2886981 DOI: 10.1093/Nar/15.14.5906  0.302
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