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Francis Sellers Collins - Publications

National Human Genome Research Institute, USA 
Human Genetics

457 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
2016 Collins FS, Anderson JM, Austin CP, Battey JF, Birnbaum LS, Briggs JP, Clayton JA, Cuthbert B, Eisinger RW, Fauci AS, Gallin JI, Gibbons GH, Glass RI, Gottesman MM, Gray PA, et al. Basic science: Bedrock of progress. Science (New York, N.Y.). 351: 1405. PMID 27013720 DOI: 10.1126/Science.351.6280.1405-A  1
2016 Lauer M, Valantine H, Collins FS. Policy: NIH push to stop sexual harassment. Nature. 531: 35. PMID 26935689 DOI: 10.1038/531035B  1
2015 Adeyemo AA, Tekola-Ayele F, Doumatey AP, Bentley AR, Chen G, Huang H, Zhou J, Shriner D, Fasanmade O, Okafor G, Eghan B, Agyenim-Boateng K, Adeleye J, Balogun W, Elkahloun A, ... ... Collins F, et al. Evaluation of Genome Wide Association Study Associated Type 2 Diabetes Susceptibility Loci in Sub Saharan Africans. Frontiers in Genetics. 6: 335. PMID 26635871 DOI: 10.3389/Fgene.2015.00335  1
2015 Green ED, Watson JD, Collins FS. Human Genome Project: Twenty-five years of big biology. Nature. 526: 29-31. PMID 26432225 DOI: 10.1038/526029A  1
2015 Quang DX, Erdos MR, Parker SC, Collins FS. Motif signatures in stretch enhancers are enriched for disease-associated genetic variants. Epigenetics & Chromatin. 8: 23. PMID 26180553 DOI: 10.1186/S13072-015-0015-7  1
2015 Fauci AS, Collins FS. NIH research: think globally. Science (New York, N.Y.). 348: 159. PMID 25859018 DOI: 10.1126/Science.Aab2733  1
2015 Vahedi G, Kanno Y, Furumoto Y, Jiang K, Parker SC, Erdos MR, Davis SR, Roychoudhuri R, Restifo NP, Gadina M, Tang Z, Ruan Y, Collins FS, Sartorelli V, O'Shea JJ. Super-enhancers delineate disease-associated regulatory nodes in T cells. Nature. 520: 558-62. PMID 25686607 DOI: 10.1038/Nature14154  1
2015 Collins FS. Exceptional opportunities in medical science: a view from the National Institutes of Health. Jama. 313: 131-2. PMID 25585318 DOI: 10.1001/Jama.2014.16736  1
2015 Valantine HA, Collins FS, Verma IM. National Institutes of Health addresses the science of diversity Proceedings of the National Academy of Sciences of the United States of America. 112: 12240-12242. DOI: 10.1073/pnas.1515612112  1
2014 Lorsch JR, Collins FS, Lippincott-Schwartz J. Cell Biology. Fixing problems with cell lines. Science (New York, N.Y.). 346: 1452-3. PMID 25525228 DOI: 10.1126/Science.1259110  1
2014 Collins FS, Wilder EL, Zerhouni E. Funding transdisciplinary research. NIH Roadmap/Common Fund at 10 years. Science (New York, N.Y.). 345: 274-6. PMID 25035478 DOI: 10.1126/Science.1255860  1
2014 Clayton JA, Collins FS. Policy: NIH to balance sex in cell and animal studies. Nature. 509: 282-3. PMID 24834516 DOI: 10.1038/509282A  1
2014 Collins FS, Hudson KL, Briggs JP, Lauer MS. PCORnet: turning a dream into reality. Journal of the American Medical Informatics Association : Jamia. 21: 576-7. PMID 24821744 DOI: 10.1136/Amiajnl-2014-002864  1
2014 Kelada SN, Carpenter DE, Aylor DL, Chines P, Rutledge H, Chesler EJ, Churchill GA, Pardo-Manuel de Villena F, Schwartz DA, Collins FS. Integrative genetic analysis of allergic inflammation in the murine lung. American Journal of Respiratory Cell and Molecular Biology. 51: 436-45. PMID 24693920 DOI: 10.1165/Rcmb.2013-0501Oc  1
2014 Rees MG, Davis MI, Shen M, Titus S, Raimondo A, Barrett A, Gloyn AL, Collins FS, Simeonov A. A panel of diverse assays to interrogate the interaction between glucokinase and glucokinase regulatory protein, two vital proteins in human disease. Plos One. 9: e89335. PMID 24586696 DOI: 10.1371/Journal.Pone.0089335  1
2014 Mahajan A, Go MJ, Zhang W, Below JE, Gaulton KJ, Ferreira T, Horikoshi M, Johnson AD, Ng MC, Prokopenko I, ... ... Collins FS, et al. Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nature Genetics. 46: 234-44. PMID 24509480 DOI: 10.1038/Ng.2897  1
2014 Service SK, Teslovich TM, Fuchsberger C, Ramensky V, Yajnik P, Koboldt DC, Larson DE, Zhang Q, Lin L, Welch R, Ding L, McLellan MD, O'Laughlin M, Fronick C, Fulton LL, ... ... Collins FS, et al. Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci. Plos Genetics. 10: e1004147. PMID 24497850 DOI: 10.1371/Journal.Pgen.1004147  1
2014 Collins FS, Tabak LA. Policy: NIH plans to enhance reproducibility. Nature. 505: 612-3. PMID 24482835 DOI: 10.1038/505612A  1
2014 Kulzer JR, Stitzel ML, Morken MA, Huyghe JR, Fuchsberger C, Kuusisto J, Laakso M, Boehnke M, Collins FS, Mohlke KL. A common functional regulatory variant at a type 2 diabetes locus upregulates ARAP1 expression in the pancreatic beta cell. American Journal of Human Genetics. 94: 186-97. PMID 24439111 DOI: 10.1016/J.Ajhg.2013.12.011  1
2014 Dimas AS, Lagou V, Barker A, Knowles JW, Mägi R, Hivert MF, Benazzo A, Rybin D, Jackson AU, Stringham HM, Song C, Fischer-Rosinsky A, Boesgaard TW, Grarup N, Abbasi FA, ... ... Collins FS, et al. Impact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneity. Diabetes. 63: 2158-71. PMID 24296717 DOI: 10.2337/Db13-0949  1
2013 Collins F, Beaudet A, Draghia-Akli R, Gruss P, Savill J, Syrota A, Dautry A, Ulfendahl M, Walport M, Onken J, Glass RI. A database on global health research in Africa. The Lancet. Global Health. 1: e64-5. PMID 25104151 DOI: 10.1016/S2214-109X(13)70012-3  1
2013 Collins FS, Hamburg MA. First FDA authorization for next-generation sequencer. The New England Journal of Medicine. 369: 2369-71. PMID 24251383 DOI: 10.1056/Nejmp1314561  1
2013 Wilder EL, Tabak LA, Pettigrew RI, Collins FS. Biomedical research: strength from diversity. Science (New York, N.Y.). 342: 798. PMID 24233704 DOI: 10.1126/Science.342.6160.798-A  1
2013 Guttmacher AE, Hirschfeld S, Collins FS. The National Children's Study--a proposed plan. The New England Journal of Medicine. 369: 1873-5. PMID 24224620 DOI: 10.1056/Nejmp1311150  1
2013 Parker SC, Stitzel ML, Taylor DL, Orozco JM, Erdos MR, Akiyama JA, van Bueren KL, Chines PS, Narisu N, Black BL, Visel A, Pennacchio LA, Collins FS, et al. Chromatin stretch enhancer states drive cell-specific gene regulation and harbor human disease risk variants. Proceedings of the National Academy of Sciences of the United States of America. 110: 17921-6. PMID 24127591 DOI: 10.1073/Pnas.1317023110  1
2013 Hudson KL, Collins FS. Biospecimen policy: Family matters. Nature. 500: 141-2. PMID 23925224 DOI: 10.1038/500141A  1
2013 Bonnycastle LL, Chines PS, Hara T, Huyghe JR, Swift AJ, Heikinheimo P, Mahadevan J, Peltonen S, Huopio H, Nuutila P, Narisu N, Goldfeder RL, Stitzel ML, Lu S, Boehnke M, ... ... Collins FS, et al. Autosomal dominant diabetes arising from a Wolfram syndrome 1 mutation. Diabetes. 62: 3943-50. PMID 23903355 DOI: 10.2337/Db13-0571  1
2013 Gartner JJ, Parker SC, Prickett TD, Dutton-Regester K, Stitzel ML, Lin JC, Davis S, Simhadri VL, Jha S, Katagiri N, Gotea V, Teer JK, Wei X, Morken MA, Bhanot UK, ... ... Collins FS, et al. Whole-genome sequencing identifies a recurrent functional synonymous mutation in melanoma. Proceedings of the National Academy of Sciences of the United States of America. 110: 13481-6. PMID 23901115 DOI: 10.1073/Pnas.1304227110  1
2013 Yaghootkar H, Lamina C, Scott RA, Dastani Z, Hivert MF, Warren LL, Stancáková A, Buxbaum SG, Lyytikäinen LP, Henneman P, Wu Y, Cheung CY, Pankow JS, Jackson AU, Gustafsson S, ... ... Collins FS, et al. Mendelian randomization studies do not support a causal role for reduced circulating adiponectin levels in insulin resistance and type 2 diabetes. Diabetes. 62: 3589-98. PMID 23835345 DOI: 10.2337/Db13-0128  1
2013 Daniels ML, Leigh MW, Davis SD, Armstrong MC, Carson JL, Hazucha M, Dell SD, Eriksson M, Collins FS, Knowles MR, Zariwala MA. Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesia. Human Mutation. 34: 1352-6. PMID 23798057 DOI: 10.1002/Humu.22371  1
2013 Randall JC, Winkler TW, Kutalik Z, Berndt SI, Jackson AU, Monda KL, Kilpeläinen TO, Esko T, Mägi R, Li S, Workalemahu T, Feitosa MF, Croteau-Chonka DC, Day FR, Fall T, ... ... Collins FS, et al. Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. Plos Genetics. 9: e1003500. PMID 23754948 DOI: 10.1371/Journal.Pgen.1003500  1
2013 Martin WJ, Glass RI, Araj H, Balbus J, Collins FS, Curtis S, Diette GB, Elwood WN, Falk H, Hibberd PL, Keown SE, Mehta S, Patrick E, Rosenbaum J, Sapkota A, et al. Household air pollution in low- and middle-income countries: health risks and research priorities. Plos Medicine. 10: e1001455. PMID 23750119 DOI: 10.1371/Journal.Pmed.1001455  1
2013 Hudson KL, Guttmacher AE, Collins FS. In support of SUPPORT--a view from the NIH. The New England Journal of Medicine. 368: 2349-51. PMID 23738511 DOI: 10.1056/Nejmp1306986  1
2013 Insel TR, Landis SC, Collins FS. Research priorities. The NIH BRAIN Initiative. Science (New York, N.Y.). 340: 687-8. PMID 23661744 DOI: 10.1126/Science.1239276  1
2013 Selby JV, Krumholz HM, Kuntz RE, Collins FS. Network news: powering clinical research. Science Translational Medicine. 5: 182fs13. PMID 23612587 DOI: 10.1126/Scitranslmed.3006298  1
2013 Mahendran Y, Vangipurapu J, Cederberg H, Stancáková A, Pihlajamäki J, Soininen P, Kangas AJ, Paananen J, Civelek M, Saleem NK, Pajukanta P, Lusis AJ, Bonnycastle LL, Morken MA, Collins FS, et al. Association of ketone body levels with hyperglycemia and type 2 diabetes in 9,398 Finnish men. Diabetes. 62: 3618-26. PMID 23557707 DOI: 10.2337/Db12-1363  1
2013 Wu Y, Waite LL, Jackson AU, Sheu WH, Buyske S, Absher D, Arnett DK, Boerwinkle E, Bonnycastle LL, Carty CL, Cheng I, Cochran B, Croteau-Chonka DC, Dumitrescu L, Eaton CB, ... ... Collins FS, et al. Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained. Plos Genetics. 9: e1003379. PMID 23555291 DOI: 10.1371/Journal.Pgen.1003379  1
2013 Pendse J, Ramachandran PV, Na J, Narisu N, Fink JL, Cagan RL, Collins FS, Baranski TJ. A Drosophila functional evaluation of candidates from human genome-wide association studies of type 2 diabetes and related metabolic traits identifies tissue-specific roles for dHHEX. Bmc Genomics. 14: 136. PMID 23445342 DOI: 10.1186/1471-2164-14-136  1
2013 Patterson AP, Tabak LA, Fauci AS, Collins FS, Howard S. Research funding. A framework for decisions about research with HPAI H5N1 viruses. Science (New York, N.Y.). 339: 1036-7. PMID 23429700 DOI: 10.1126/Science.1236194  1
2013 Huyghe JR, Jackson AU, Fogarty MP, Buchkovich ML, Stančáková A, Stringham HM, Sim X, Yang L, Fuchsberger C, Cederberg H, Chines PS, Teslovich TM, Romm JM, Ling H, McMullen I, ... ... Collins FS, et al. Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion. Nature Genetics. 45: 197-201. PMID 23263489 DOI: 10.1038/Ng.2507  1
2013 Vickers KC, Shoucri BM, Levin MG, Wu H, Pearson DS, Osei-Hwedieh D, Collins FS, Remaley AT, Sethupathy P. MicroRNA-27b is a regulatory hub in lipid metabolism and is altered in dyslipidemia. Hepatology (Baltimore, Md.). 57: 533-42. PMID 22777896 DOI: 10.1002/Hep.25846  1
2012 Rao MS, Collins FS. Steering a new course for stem cell research: NIH's intramural Center for Regenerative Medicine. Stem Cells Translational Medicine. 1: 15-7. PMID 23197635 DOI: 10.5966/Sctm.2011-0032  1
2012 Gordon LB, Cao K, Collins FS. Progeria: translational insights from cell biology. The Journal of Cell Biology. 199: 9-13. PMID 23027899 DOI: 10.1083/Jcb.201207072  1
2012 Rodgers GP, Collins FS. The next generation of obesity research: no time to waste. Jama. 308: 1095-6. PMID 22990265 DOI: 10.1001/2012.Jama.11853  1
2012 Bradley A, Anastassiadis K, Ayadi A, Battey JF, Bell C, Birling MC, Bottomley J, Brown SD, Bürger A, Bult CJ, Bushell W, Collins FS, Desaintes C, Doe B, Economides A, et al. The mammalian gene function resource: the International Knockout Mouse Consortium. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 23: 580-6. PMID 22968824 DOI: 10.1007/S00335-012-9422-2  1
2012 Collins FS. NIH basics. Science (New York, N.Y.). 337: 503. PMID 22859455 DOI: 10.1126/science.1227820  1
2012 Fauci AS, Collins FS. Benefits and risks of influenza research: lessons learned. Science (New York, N.Y.). 336: 1522-3. PMID 22723407 DOI: 10.1126/Science.1224305  1
2012 Perry JR, Voight BF, Yengo L, Amin N, Dupuis J, Ganser M, Grallert H, Navarro P, Li M, Qi L, Steinthorsdottir V, Scott RA, Almgren P, Arking DE, Aulchenko Y, ... ... Collins FS, et al. Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases. Plos Genetics. 8: e1002741. PMID 22693455 DOI: 10.1371/Journal.Pgen.1002741  1
2012 Manning AK, Hivert MF, Scott RA, Grimsby JL, Bouatia-Naji N, Chen H, Rybin D, Liu CT, Bielak LF, Prokopenko I, Amin N, Barnes D, Cadby G, Hottenga JJ, Ingelsson E, ... ... Collins FS, et al. A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Nature Genetics. 44: 659-69. PMID 22581228 DOI: 10.1038/Ng.2274  1
2012 Stancáková A, Civelek M, Saleem NK, Soininen P, Kangas AJ, Cederberg H, Paananen J, Pihlajamäki J, Bonnycastle LL, Morken MA, Boehnke M, Pajukanta P, Lusis AJ, Collins FS, Kuusisto J, et al. Hyperglycemia and a common variant of GCKR are associated with the levels of eight amino acids in 9,369 Finnish men. Diabetes. 61: 1895-902. PMID 22553379 DOI: 10.2337/Db11-1378  1
2012 Stefanovski D, Youn JH, Rees M, Watanabe RM, Ader M, Ionut V, Jackson AU, Boehnke M, Collins FS, Bergman RN. Estimating hepatic glucokinase activity using a simple model of lactate kinetics. Diabetes Care. 35: 1015-20. PMID 22456868 DOI: 10.2337/Dc11-1540  1
2012 Scott RA, Chu AY, Grarup N, Manning AK, Hivert MF, Shungin D, Tönjes A, Yesupriya A, Barnes D, Bouatia-Naji N, Glazer NL, Jackson AU, Kutalik Z, Lagou V, Marek D, ... ... Collins FS, et al. No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels. Diabetes. 61: 1291-6. PMID 22415877 DOI: 10.2337/Db11-0973  1
2012 Manolio TA, Weis BK, Cowie CC, Hoover RN, Hudson K, Kramer BS, Berg C, Collins R, Ewart W, Gaziano JM, Hirschfeld S, Marcus PM, Masys D, McCarty CA, McLaughlin J, ... ... Collins FS, et al. New models for large prospective studies: is there a better way? American Journal of Epidemiology. 175: 859-66. PMID 22411865 DOI: 10.1093/Aje/Kwr453  1
2012 Kelada SN, Aylor DL, Peck BC, Ryan JF, Tavarez U, Buus RJ, Miller DR, Chesler EJ, Threadgill DW, Churchill GA, Pardo-Manuel de Villena F, Collins FS. Genetic analysis of hematological parameters in incipient lines of the collaborative cross. G3 (Bethesda, Md.). 2: 157-65. PMID 22384394 DOI: 10.1534/G3.111.001776  1
2012 Iraqi FA, Mahajne M, Salaymah Y, Sandovski H, Tayem H, Vered K, Balmer L, Hall M, Manship G, Morahan G, Pettit K, Scholten J, Tweedie K, Wallace A, Weerasekera L, ... ... Collins FS, et al. The genome architecture of the collaborative cross mouse genetic reference population Genetics. 190: 389-401. PMID 22345608 DOI: 10.1534/Genetics.111.132639  1
2012 Conneely KN, Capell BC, Erdos MR, Sebastiani P, Solovieff N, Swift AJ, Baldwin CT, Budagov T, Barzilai N, Atzmon G, Puca AA, Perls TT, Geesaman BJ, Boehnke M, Collins FS. Human longevity and common variations in the LMNA gene: a meta-analysis. Aging Cell. 11: 475-81. PMID 22340368 DOI: 10.1111/J.1474-9726.2012.00808.X  1
2012 Graziotto JJ, Cao K, Collins FS, Krainc D. Rapamycin activates autophagy in Hutchinson-Gilford progeria syndrome: implications for normal aging and age-dependent neurodegenerative disorders. Autophagy. 8: 147-51. PMID 22170152 DOI: 10.4161/Auto.8.1.18331  1
2011 Bobb JF, Scharfstein DO, Daniels MJ, Collins FS, Kelada S. Multiple imputation of missing phenotype data for QTL mapping. Statistical Applications in Genetics and Molecular Biology. 10: Article 29. PMID 24683667 DOI: 10.2202/1544-6115.1676  1
2011 Melgar MF, Collins FS, Sethupathy P. Discovery of active enhancers through bidirectional expression of short transcripts. Genome Biology. 12: R113. PMID 22082242 DOI: 10.1186/Gb-2011-12-11-R113  1
2011 Martin WJ, Glass RI, Balbus JM, Collins FS. Public health. A major environmental cause of death. Science (New York, N.Y.). 334: 180-1. PMID 21998373 DOI: 10.1126/Science.1213088  1
2011 Tabak LA, Collins FS. Sociology. Weaving a richer tapestry in biomedical science. Science (New York, N.Y.). 333: 940-1. PMID 21852476 DOI: 10.1126/Science.1211704  1
2011 Collins FS. Reengineering translational science: the time is right. Science Translational Medicine. 3: 90cm17. PMID 21734173 DOI: 10.1126/Scitranslmed.3002747  1
2011 Cao K, Graziotto JJ, Blair CD, Mazzulli JR, Erdos MR, Krainc D, Collins FS. Rapamycin reverses cellular phenotypes and enhances mutant protein clearance in Hutchinson-Gilford progeria syndrome cells. Science Translational Medicine. 3: 89ra58. PMID 21715679 DOI: 10.1126/Scitranslmed.3002346  1
2011 Cao K, Blair CD, Faddah DA, Kieckhaefer JE, Olive M, Erdos MR, Nabel EG, Collins FS. Progerin and telomere dysfunction collaborate to trigger cellular senescence in normal human fibroblasts. The Journal of Clinical Investigation. 121: 2833-44. PMID 21670498 DOI: 10.1172/Jci43578  1
2011 Collins FS. Mining for therapeutic gold. Nature Reviews. Drug Discovery. 10: 397. PMID 21629277 DOI: 10.1038/Nrd3461  1
2011 Stančáková A, Paananen J, Soininen P, Kangas AJ, Bonnycastle LL, Morken MA, Collins FS, Jackson AU, Boehnke ML, Kuusisto J, Ala-Korpela M, Laakso M. Effects of 34 risk loci for type 2 diabetes or hyperglycemia on lipoprotein subclasses and their composition in 6,580 nondiabetic Finnish men. Diabetes. 60: 1608-16. PMID 21421807 DOI: 10.2337/Db10-1655  1
2011 Aylor DL, Valdar W, Foulds-Mathes W, Buus RJ, Verdugo RA, Baric RS, Ferris MT, Frelinger JA, Heise M, Frieman MB, Gralinski LE, Bell TA, Didion JD, Hua K, Nehrenberg DL, ... ... Collins FS, et al. Genetic analysis of complex traits in the emerging Collaborative Cross. Genome Research. 21: 1213-22. PMID 21406540 DOI: 10.1101/Gr.111310.110  1
2011 Verstraeten VLRM, Peckham LA, Olive M, Capell BC, Collins FS, Nabel EG, Young SG, Fong LG, Lammerding J. Protein farnesylation inhibitors cause donut-shaped cell nuclei attributable to a centrosome separation defect Proceedings of the National Academy of Sciences of the United States of America. 108: 4997-5002. PMID 21383178 DOI: 10.1073/Pnas.1019532108  1
2011 Kelada SN, Wilson MS, Tavarez U, Kubalanza K, Borate B, Whitehead GS, Maruoka S, Roy MG, Olive M, Carpenter DE, Brass DM, Wynn TA, Cook DN, Evans CM, Schwartz DA, ... Collins FS, et al. Strain-dependent genomic factors affect allergen-induced airway hyperresponsiveness in mice. American Journal of Respiratory Cell and Molecular Biology. 45: 817-24. PMID 21378263 DOI: 10.1165/Rcmb.2010-0315Oc  1
2011 Collins FS. Genome-sequencing anniversary. Faces of the genome. Science (New York, N.Y.). 331: 546. PMID 21292963 DOI: 10.1126/Science.1202894  1
2011 Jafar-Mohammadi B, Groves CJ, Gjesing AP, Herrera BM, Winckler W, Stringham HM, Morris AP, Lauritzen T, Doney AS, Morris AD, Weedon MN, Swift AJ, Kuusisto J, Laakso M, Altshuler D, ... ... Collins FS, et al. A role for coding functional variants in HNF4A in type 2 diabetes susceptibility. Diabetologia. 54: 111-9. PMID 20878384 DOI: 10.1007/S00125-010-1916-4  1
2011 Martin WJ, Glass RI, Balbus JM, Collins FS. Cultivating a demand for clean cookstoves - Response Science. 334: 1637. DOI: 10.1126/Science.334.6063.1637-A  1
2011 Collins FS. Inside the National Institutes of Health Biopharm International. 24.  1
2010 Collins FS. Change, change, change: heeding the call. Molecular Biology of the Cell. 21: 3793-4. PMID 21079014 DOI: 10.1091/Mbc.E10-08-0726  1
2010 Stitzel ML, Sethupathy P, Pearson DS, Chines PS, Song L, Erdos MR, Welch R, Parker SC, Boyle AP, Scott LJ, Margulies EH, Boehnke M, Furey TS, Crawford GE, ... Collins FS, et al. Global epigenomic analysis of primary human pancreatic islets provides insights into type 2 diabetes susceptibility loci. Cell Metabolism. 12: 443-55. PMID 21035756 DOI: 10.1016/J.Cmet.2010.09.012  1
2010 Abecasis GR, Altshuler D, Auton A, Brooks LD, Durbin RM, Gibbs RA, Hurles ME, McVean GA. A map of human genome variation from population-scale sequencing. Nature. 467: 1061-73. PMID 20981092 DOI: 10.1038/Nature09534  1
2010 Frieden TR, Collins FS. Intentional infection of vulnerable populations in 1946-1948: another tragic history lesson. Jama. 304: 2063-4. PMID 20937719 DOI: 10.1001/Jama.2010.1554  1
2010 Soranzo N, Sanna S, Wheeler E, Gieger C, Radke D, Dupuis J, Bouatia-Naji N, Langenberg C, Prokopenko I, Stolerman E, Sandhu MS, Heeney MM, Devaney JM, Reilly MP, Ricketts SL, ... ... Collins FS, et al. Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways. Diabetes. 59: 3229-39. PMID 20858683 DOI: 10.2337/Db10-0502  1
2010 Olive M, Harten I, Mitchell R, Beers JK, Djabali K, Cao K, Erdos MR, Blair C, Funke B, Smoot L, Gerhard-Herman M, Machan JT, Kutys R, Virmani R, Collins FS, et al. Cardiovascular pathology in Hutchinson-Gilford progeria: correlation with the vascular pathology of aging. Arteriosclerosis, Thrombosis, and Vascular Biology. 30: 2301-9. PMID 20798379 DOI: 10.1161/Atvbaha.110.209460  1
2010 Clancy C, Collins FS. Patient-centered outcomes research institute: The intersection of science and health care Science Translational Medicine. 2. PMID 20574065 DOI: 10.1126/Scitranslmed.3001235  1
2010 Hamburg MA, Collins FS. The path to personalized medicine New England Journal of Medicine. 363: 301-304. PMID 20551152 DOI: 10.1056/Nejmp1006304  1
2010 Lauer MS, Collins FS. Using science to improve the nation's health system: NIH's commitment to comparative effectiveness research Jama - Journal of the American Medical Association. 303: 2182-2183. PMID 20516419 DOI: 10.1001/jama.2010.726  1
2010 Feero WG, Guttmacher AE, Collins FS. Genomic medicine - An updated primer New England Journal of Medicine. 362: 2001-2011. PMID 20505179 DOI: 10.1056/Nejmra0907175  1
2010 Rockey SJ, Collins FS. Managing financial conflict of interest in biomedical research Jama - Journal of the American Medical Association. 303: 2400-2402. PMID 20498237 DOI: 10.1001/Jama.2010.774  1
2010 McDaniell R, Lee BK, Song L, Liu Z, Boyle AP, Erdos MR, Scott LJ, Morken MA, Kucera KS, Battenhouse A, Keefe D, Collins FS, Willard HF, Lieb JD, Furey TS, et al. Heritable individual-specific and allele-specific chromatin signatures in humans. Science (New York, N.Y.). 328: 235-9. PMID 20299549 DOI: 10.1126/Science.1184655  1
2010 Ingelsson E, Langenberg C, Hivert MF, Prokopenko I, Lyssenko V, Dupuis J, Mägi R, Sharp S, Jackson AU, Assimes TL, Shrader P, Knowles JW, Zethelius B, Abbasi FA, Bergman RN, ... ... Collins FS, et al. Detailed physiologic characterization reveals diverse mechanisms for novel genetic Loci regulating glucose and insulin metabolism in humans. Diabetes. 59: 1266-75. PMID 20185807 DOI: 10.2337/Db09-1568  1
2010 Saxena R, Hivert MF, Langenberg C, Tanaka T, Pankow JS, Vollenweider P, Lyssenko V, Bouatia-Naji N, Dupuis J, Jackson AU, Kao WH, Li M, Glazer NL, Manning AK, Luan J, ... ... Collins FS, et al. Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. Nature Genetics. 42: 142-8. PMID 20081857 DOI: 10.1038/Ng.521  1
2010 Collins FS. Opportunities for research and NIH Science. 327: 36-37. PMID 20044560 DOI: 10.1126/Science.1185055  1
2009 Rosenfeld MA, Collins FS. Gene therapy for cystic fibrosis. 1996 Chest. 136. PMID 20162780  1
2009 Taimen P, Pfleghaar K, Shimi T, Möller D, Ben-Harush K, Erdos MR, Adam SA, Herrmann H, Medalia O, Collins FS, Goldman AE, Goldman RD. A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization. Proceedings of the National Academy of Sciences of the United States of America. 106: 20788-93. PMID 19926845 DOI: 10.1073/Pnas.0911895106  1
2009 Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, McCarthy MI, Ramos EM, Cardon LR, Chakravarti A, Cho JH, Guttmacher AE, Kong A, Kruglyak L, Mardis E, et al. Finding the missing heritability of complex diseases. Nature. 461: 747-53. PMID 19812666 DOI: 10.1038/Nature08494  1
2009 Guttmacher AE, Nabel EG, Collins FS. Why data-sharing policies matter Proceedings of the National Academy of Sciences of the United States of America. 106: 16894. PMID 19805161 DOI: 10.1073/Pnas.0910378106  1
2009 Temple G, Gerhard DS, Rasooly R, Feingold EA, Good PJ, Robinson C, Mandich A, Derge JG, Lewis J, Shoaf D, Collins FS, Jang W, Wagner L, Shenmen CM, et al. The completion of the Mammalian Gene Collection (MGC). Genome Research. 19: 2324-33. PMID 19767417 DOI: 10.1101/Gr.095976.109  1
2009 Goode EL, Szabo C, Prokunina-Olsson L, Vierkant RA, Fredericksen ZS, Collins FS, White KL, Schmidt M, Fridley BL, Couch FJ. No association between a candidate TCF7L2 variant and risk of breast or ovarian cancer. Bmc Cancer. 9: 312. PMID 19732438 DOI: 10.1186/1471-2407-9-312  1
2009 Manolio TA, Collins FS. The HapMap and genome-wide association studies in diagnosis and therapy. Annual Review of Medicine. 60: 443-56. PMID 19630580 DOI: 10.1146/Annurev.Med.60.061907.093117  1
2009 Khoury MJ, McBride CM, Schully SD, Ioannidis JP, Feero WG, Janssens AC, Gwinn M, Simons-Morton DG, Bernhardt JM, Cargill M, Chanock SJ, Church GM, Coates RJ, Collins FS, Croyle RT, et al. The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 11: 559-67. PMID 19617843 DOI: 10.1097/Gim.0B013E3181B13A6C  1
2009 Prokunina-Olsson L, Welch C, Hansson O, Adhikari N, Scott LJ, Usher N, Tong M, Sprau A, Swift A, Bonnycastle LL, Erdos MR, He Z, Saxena R, Harmon B, Kotova O, ... ... Collins FS, et al. Tissue-specific alternative splicing of TCF7L2. Human Molecular Genetics. 18: 3795-804. PMID 19602480 DOI: 10.1093/Hmg/Ddp321  1
2009 Stancáková A, Kuulasmaa T, Paananen J, Jackson AU, Bonnycastle LL, Collins FS, Boehnke M, Kuusisto J, Laakso M. Association of 18 confirmed susceptibility loci for type 2 diabetes with indices of insulin release, proinsulin conversion, and insulin sensitivity in 5,327 nondiabetic Finnish men. Diabetes. 58: 2129-36. PMID 19502414 DOI: 10.2337/Db09-0117  1
2009 Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, Manolio TA. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proceedings of the National Academy of Sciences of the United States of America. 106: 9362-7. PMID 19474294 DOI: 10.1073/Pnas.0903103106  1
2009 Newton-Cheh C, Johnson T, Gateva V, Tobin MD, Bochud M, Coin L, Najjar SS, Zhao JH, Heath SC, Eyheramendy S, Papadakis K, Voight BF, Scott LJ, Zhang F, Farrall M, ... ... Collins FS, et al. Genome-wide association study identifies eight loci associated with blood pressure. Nature Genetics. 41: 666-76. PMID 19430483 DOI: 10.1038/Ng.361  1
2009 Willer CJ, Speliotes EK, Loos RJ, Li S, Lindgren CM, Heid IM, Berndt SI, Elliott AL, Jackson AU, Lamina C, Lettre G, Lim N, Lyon HN, McCarroll SA, Papadakis K, ... ... Collins FS, et al. Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nature Genetics. 41: 25-34. PMID 19079261 DOI: 10.1038/Ng.287  1
2009 Prokopenko I, Langenberg C, Florez JC, Saxena R, Soranzo N, Thorleifsson G, Loos RJ, Manning AK, Jackson AU, Aulchenko Y, Potter SC, Erdos MR, Sanna S, Hottenga JJ, Wheeler E, ... ... Collins FS, et al. Variants in MTNR1B influence fasting glucose levels. Nature Genetics. 41: 77-81. PMID 19060907 DOI: 10.1038/Ng.290  1
2009 Kathiresan S, Willer CJ, Peloso GM, Demissie S, Musunuru K, Schadt EE, Kaplan L, Bennett D, Li Y, Tanaka T, Voight BF, Bonnycastle LL, Jackson AU, Crawford G, Surti A, ... ... Collins FS, et al. Common variants at 30 loci contribute to polygenic dyslipidemia. Nature Genetics. 41: 56-65. PMID 19060906 DOI: 10.1038/Ng.291  1
2009 Fink L, Collins FS. The human genome project: Evolving status and emerging opportunities for disease prevention Genetics and Public Health in the 21st Century: Using Genetic Information to Improve Health and Prevent Disease. DOI: 10.1093/acprof:oso/9780195128307.003.0003  1
2009 Capell BC, Olive M, Erdos MR, Cao K, Faddah DA, Tavarez UL, Conneely KN, Qu X, San H, Ganesh SK, Chen X, Avallone H, Kolodgie FD, Virmani R, Nabel EG, ... Collins FS, et al. A farnesyltransferase inhibitor prevents both the onset and late progression of cardiovascular disease in a progeria mouse model (Proceedings of the National Academy of Sciences of the United States of America (2008) 105, (15902-15907) DOI: 10.1073/pnas.0807840105) Proceedings of the National Academy of Sciences of the United States of America. 106: 13143. DOI: 10.1073/Pnas.0907672106  1
2008 Capell BC, Olive M, Erdos MR, Cao K, Faddah DA, Tavarez UL, Conneely KN, Qu X, San H, Ganesh SK, Chen X, Avallone H, Kolodgie FD, Virmani R, Nabel EG, ... Collins FS, et al. A farnesyltransferase inhibitor prevents both the onset and late progression of cardiovascular disease in a progeria mouse model. Proceedings of the National Academy of Sciences of the United States of America. 105: 15902-7. PMID 18838683 DOI: 10.1073/Pnas.0807840105  1
2008 Sethupathy P, Collins FS. MicroRNA target site polymorphisms and human disease. Trends in Genetics : Tig. 24: 489-97. PMID 18778868 DOI: 10.1016/J.Tig.2008.07.004  1
2008 Collins FS. Retrospective: Victor A. McKusick (1921-2008) Science (New York, N.Y.). 321: 925. PMID 18703732 DOI: 10.1126/Science.1163901  1
2008 Hudson KL, Holohan MK, Collins FS. Keeping pace with the times - The genetic information nondiscrimination act of 2008 New England Journal of Medicine. 358: 2661-2663. PMID 18565857 DOI: 10.1056/Nejmp0803964  1
2008 Chen WM, Erdos MR, Jackson AU, Saxena R, Sanna S, Silver KD, Timpson NJ, Hansen T, Orrù M, Grazia Piras M, Bonnycastle LL, Willer CJ, Lyssenko V, Shen H, Kuusisto J, ... ... Collins FS, et al. Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels. The Journal of Clinical Investigation. 118: 2620-8. PMID 18521185 DOI: 10.1172/Jci34566  1
2008 Manolio TA, Brooks LD, Collins FS. A HapMap harvest of insights into the genetics of common disease. The Journal of Clinical Investigation. 118: 1590-605. PMID 18451988 DOI: 10.1172/Jci34772  1
2008 Feero WG, Guttmacher AE, Collins FS. The genome gets personal - Almost Jama - Journal of the American Medical Association. 299: 1351-1352. PMID 18349096 DOI: 10.1001/Jama.299.11.1351  1
2008 Shen HC, Rosen JE, Yang LM, Savage SA, Burns AL, Mateo CM, Agarwal SK, Chandrasekharappa SC, Spiegel AM, Collins FS, Marx SJ, Libutti SK. Parathyroid tumor development involves deregulation of homeobox genes. Endocrine-Related Cancer. 15: 267-75. PMID 18310293 DOI: 10.1677/Erc-07-0191  1
2008 Collins FS, Gray GM, Bucher JR. Transforming environmental health protection Science. 319: 906-907. PMID 18276874 DOI: 10.1126/Science.1154619  1
2008 Merideth MA, Gordon LB, Clauss S, Sachdev V, Smith ACM, Perry MB, Brewer CC, Zalewski C, Kim HJ, Solomon B, Brooks BP, Gerber LH, Turner ML, Domingo DL, Hart TC, ... ... Collins FS, et al. Phenotype and course of Hutchinson-Gilford progeria syndrome New England Journal of Medicine. 358: 592-604. PMID 18256394 DOI: 10.1056/Nejmoa0706898  1
2008 Sanna S, Jackson AU, Nagaraja R, Willer CJ, Chen WM, Bonnycastle LL, Shen H, Timpson N, Lettre G, Usala G, Chines PS, Stringham HM, Scott LJ, Dei M, Lai S, ... ... Collins FS, et al. Common variants in the GDF5-UQCC region are associated with variation in human height. Nature Genetics. 40: 198-203. PMID 18193045 DOI: 10.1038/Ng.74  1
2008 Willer CJ, Sanna S, Jackson AU, Scuteri A, Bonnycastle LL, Clarke R, Heath SC, Timpson NJ, Najjar SS, Stringham HM, Strait J, Duren WL, Maschio A, Busonero F, Mulas A, ... ... Collins FS, et al. Newly identified loci that influence lipid concentrations and risk of coronary artery disease. Nature Genetics. 40: 161-9. PMID 18193043 DOI: 10.1038/Ng.76  1
2008 Merideth MA, Collins FS, Gahl WA. The authors reply New England Journal of Medicine. 358: 2410-2411.  1
2007 Feero WG, Manolio TA, Guttmacher AE, Collins FS. Validity of reported genetic risk factors for acute coronary syndrome. Jama. 298: 1757; author reply 1. PMID 17940226 DOI: 10.1001/jama.298.15.1757-a  1
2007 Manolio TA, Rodriguez LL, Brooks L, Abecasis G, Ballinger D, Daly M, Donnelly P, Faraone SV, Frazer K, Gabriel S, Gejman P, ... ... Collins FS, et al. New models of collaboration in genome-wide association studies: the Genetic Association Information Network. Nature Genetics. 39: 1045-51. PMID 17728769 DOI: 10.1038/Ng2127  1
2007 Lowrance WW, Collins FS. Identifiability in genomic research Science. 317: 600-602. PMID 17673640 DOI: 10.1126/Science.1147699  1
2007 Capell BC, Collins FS, Nabel EG. Mechanisms of cardiovascular disease in accelerated aging syndromes Circulation Research. 101: 13-26. PMID 17615378 DOI: 10.1161/Circresaha.107.153692  1
2007 Birney E, Stamatoyannopoulos JA, Dutta A, Guigó R, Gingeras TR, Margulies EH, Weng Z, Snyder M, Dermitzakis ET, Thurman RE, Kuehn MS, Taylor CM, Neph S, Koch CM, ... ... Collins FS, et al. Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Nature. 447: 799-816. PMID 17571346 DOI: 10.1038/Nature05874  1
2007 Chanock SJ, Manolio T, Boehnke M, Boerwinkle E, Hunter DJ, Thomas G, Hirschhorn JN, Abecasis G, Altshuler D, Bailey-Wilson JE, Brooks LD, Cardon LR, Daly M, Donnelly P, ... ... Collins FS, et al. Replicating genotype-phenotype associations. Nature. 447: 655-60. PMID 17554299 DOI: 10.1038/447655A  1
2007 Scott LJ, Mohlke KL, Bonnycastle LL, Willer CJ, Li Y, Duren WL, Erdos MR, Stringham HM, Chines PS, Jackson AU, Prokunina-Olsson L, Ding CJ, Swift AJ, Narisu N, Hu T, ... ... Collins FS, et al. A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science (New York, N.Y.). 316: 1341-5. PMID 17463248 DOI: 10.1126/Science.1142382  1
2007 Collins FS, Finnell RH, Rossant J, Wurst W. A new partner for the international knockout mouse consortium. Cell. 129: 235. PMID 17448981 DOI: 10.1016/J.Cell.2007.04.007  1
2007 Agarwal SK, Impey S, McWeeney S, Scacheri PC, Collins FS, Goodman RH, Spiegel AM, Marx SJ. Distribution of menin-occupied regions in chromatin specifies a broad role of menin in transcriptional regulation. Neoplasia (New York, N.Y.). 9: 101-7. PMID 17356705 DOI: 10.1593/Neo.06706  1
2007 Collins FS, Barker AD. Mapping the cancer genome Scientific American. 296: 50-57. PMID 17348159 DOI: 10.1038/Scientificamerican0307-50  1
2007 Sieving PA, Collins FS. Genetic ophthalmology and the era of clinical care. Jama. 297: 733-6. PMID 17315303 DOI: 10.1001/Jama.297.7.733  1
2007 Ozawa A, Agarwal SK, Mateo CM, Burns AL, Rice TS, Kennedy PA, Quigley CM, Simonds WF, Weinstein LS, Chandrasekharappa SC, Collins FS, Spiegel AM, Marx SJ. The parathyroid/pituitary variant of multiple endocrine neoplasia type 1 usually has causes other than p27Kip1 mutations. The Journal of Clinical Endocrinology and Metabolism. 92: 1948-51. PMID 17299066 DOI: 10.1210/Jc.2006-2563  1
2007 Manolio TA, Collins FS. Genes, environment, health, and disease: facing up to complexity. Human Heredity. 63: 63-6. PMID 17283435 DOI: 10.1159/000099178  1
2007 Collins FS, Manolio TA. Merging and emerging cohorts: necessary but not sufficient. Nature. 445: 259. PMID 17230172 DOI: 10.1038/445259A  1
2007 Willer CJ, Bonnycastle LL, Conneely KN, Duren WL, Jackson AU, Scott LJ, Narisu N, Chines PS, Skol A, Stringham HM, Petrie J, Erdos MR, Swift AJ, Enloe ST, Sprau AG, ... ... Collins FS, et al. Screening of 134 single nucleotide polymorphisms (SNPs) previously associated with type 2 diabetes replicates association with 12 SNPs in nine genes. Diabetes. 56: 256-64. PMID 17192490 DOI: 10.2337/Db06-0461  1
2007 Shtir C, Nagakawa IS, Duren WL, Conneely KN, Scott LJ, Silander K, Valle TT, Tuomilehto J, Buchanan TA, Bergman RN, Collins FS, Boehnke M, Watanabe RM. Subsets of Finns with high HDL to total cholesterol ratio show evidence for linkage to type 2 diabetes on chromosome 6q. Human Heredity. 63: 17-25. PMID 17179727 DOI: 10.1159/000097927  1
2007 Baffoe-Bonnie AB, Kittles RA, Gillanders E, Ou L, George A, Robbins C, Ahaghotu C, Bennett J, Boykin W, Hoke G, Mason T, Pettaway C, Vijayakumar S, Weinrich S, Jones MP, ... ... Collins FS, et al. Genome-wide linkage of 77 families from the African American Hereditary Prostate Cancer study (AAHPC). The Prostate. 67: 22-31. PMID 17031815 DOI: 10.1002/Pros.20456  1
2006 Capell BC, Collins FS. Human laminopathies: Nuclei gone genetically awry Nature Reviews Genetics. 7: 940-952. PMID 17139325 DOI: 10.1038/Nrg1906  1
2006 Manolio TA, Bailey-Wilson JE, Collins FS. Genes, environment and the value of prospective cohort studies. Nature Reviews. Genetics. 7: 812-20. PMID 16983377 DOI: 10.1038/Nrg1919  1
2006 Scott LJ, Bonnycastle LL, Willer CJ, Sprau AG, Jackson AU, Narisu N, Duren WL, Chines PS, Stringham HM, Erdos MR, Valle TT, Tuomilehto J, Bergman RN, Mohlke KL, Collins FS, et al. Association of transcription factor 7-like 2 (TCF7L2) variants with type 2 diabetes in a Finnish sample. Diabetes. 55: 2649-53. PMID 16936217 DOI: 10.2337/Db06-0341  1
2006 Bonnycastle LL, Willer CJ, Conneely KN, Jackson AU, Burrill CP, Watanabe RM, Chines PS, Narisu N, Scott LJ, Enloe ST, Swift AJ, Duren WL, Stringham HM, Erdos MR, Riebow NL, ... ... Collins FS, et al. Common variants in maturity-onset diabetes of the young genes contribute to risk of type 2 diabetes in Finns. Diabetes. 55: 2534-40. PMID 16936201 DOI: 10.2337/Db06-0178  1
2006 Cerrato A, Parisi M, Anna SS, Missirlis F, Guru S, Agarwal S, Sturgill D, Talbot T, Spiegel A, Collins F, Chandrasekharappa S, Marx S, Oliver B. Genetic interactions between Drosophila melanogaster menin and Jun/Fos Developmental Biology. 298: 59-70. PMID 16930585 DOI: 10.1016/J.Ydbio.2006.06.013  1
2006 Collins FS. No longer just looking under the lamppost American Journal of Human Genetics. 79: 421-426. PMID 16909378 DOI: 10.1086/507611  1
2006 Lewinski MK, Yamashita M, Emerman M, Ciuffi A, Marshall H, Crawford G, Collins F, Shinn P, Leipzig J, Hannenhalli S, Berry CC, Ecker JR, Bushman FD. Retroviral DNA integration: viral and cellular determinants of target-site selection. Plos Pathogens. 2: e60. PMID 16789841 DOI: 10.1371/Journal.Ppat.0020060  1
2006 Shumaker DK, Dechat T, Kohlmaier A, Adam SA, Bozovsky MR, Erdos MR, Eriksson M, Goldman AE, Khuon S, Collins FS, Jenuwein T, Goldman RD. Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging. Proceedings of the National Academy of Sciences of the United States of America. 103: 8703-8. PMID 16738054 DOI: 10.1073/Pnas.0602569103  1
2006 Bernat JA, Crawford GE, Ogurtsov AY, Collins FS, Ginsburg D, Kondrashov AS. Distant conserved sequences flanking endothelial-specific promoters contain tissue-specific DNase-hypersensitive sites and over-represented motifs. Human Molecular Genetics. 15: 2098-105. PMID 16723375 DOI: 10.1093/Hmg/Ddl133  1
2006 Alexander DF, Alving BM, Battey JF, Berg JM, Collins FS, Fauci AS, Gallin JI, Grady PA, Hodes RJ, Hrynkow SH, Insel TR, Jones JF, Katz SI, Landis SC, Li TK, et al. Response to: "Rescuing the NIH before it is too late". The Journal of Clinical Investigation. 116: 1462-3. PMID 16648877 DOI: 10.1172/Jci28894  1
2006 Scacheri PC, Davis S, Odom DT, Crawford GE, Perkins S, Halawi MJ, Agarwal SK, Marx SJ, Spiegel AM, Meltzer PS, Collins FS. Genome-wide analysis of menin binding provides insights into MEN1 tumorigenesis. Plos Genetics. 2: e51. PMID 16604156 DOI: 10.1371/Journal.Pgen.0020051  1
2006 Varga R, Eriksson M, Erdos MR, Olive M, Harten I, Kolodgie F, Capell BC, Cheng J, Faddah D, Perkins S, Avallone H, San H, Qu X, Ganesh S, Gordon LB, ... ... Collins FS, et al. Progressive vascular smooth muscle cell defects in a mouse model of Hutchinson-Gilford progeria syndrome. Proceedings of the National Academy of Sciences of the United States of America. 103: 3250-5. PMID 16492728 DOI: 10.1073/Pnas.0600012103  1
2006 Willer CJ, Scott LJ, Bonnycastle LL, Jackson AU, Chines P, Pruim R, Bark CW, Tsai YY, Pugh EW, Doheny KF, Kinnunen L, Mohlke KL, Valle TT, Bergman RN, Tuomilehto J, ... Collins FS, et al. Tag SNP selection for Finnish individuals based on the CEPH Utah HapMap database. Genetic Epidemiology. 30: 180-90. PMID 16374835 DOI: 10.1002/Gepi.20131  1
2006 Crawford GE, Holt IE, Whittle J, Webb BD, Tai D, Davis S, Margulies EH, Chen Y, Bernat JA, Ginsburg D, Zhou D, Luo S, Vasicek TJ, Daly MJ, Wolfsberg TG, ... Collins FS, et al. Genome-wide mapping of DNase hypersensitive sites using massively parallel signature sequencing (MPSS). Genome Research. 16: 123-31. PMID 16344561 DOI: 10.1101/Gr.4074106  1
2006 Kittles RA, Baffoe-Bonnie AB, Moses TY, Robbins CM, Ahaghotu C, Huusko P, Pettaway C, Vijayakumar S, Bennett J, Hoke G, Mason T, Weinrich S, Trent JM, Collins FS, Mousses S, et al. A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history. Journal of Medical Genetics. 43: 507-11. PMID 16155194 DOI: 10.1136/Jmg.2005.035790  1
2006 Bonilla C, Panguluri RK, Taliaferro-Smith L, Argyropoulos G, Chen G, Adeyemo AA, Amoah A, Owusu S, Acheampong J, Agyenim-Boateng K, Eghan BA, Oli J, Okafor G, Abbiyesuku F, Johnson T, ... ... Collins FS, et al. Agouti-related protein promoter variant associated with leanness and decreased risk for diabetes in West Africans. International Journal of Obesity (2005). 30: 715-21. PMID 16130030 DOI: 10.1038/Sj.Ijo.0803047  1
2005 Guttmacher AE, Collins FS. Realizing the promise of genomics in biomedical research Journal of the American Medical Association. 294: 1399-1402. PMID 16174701 DOI: 10.1001/jama.294.11.1399  1
2005 Mohlke KL, Jackson AU, Scott LJ, Peck EC, Suh YD, Chines PS, Watanabe RM, Buchanan TA, Conneely KN, Erdos MR, Narisu N, Enloe S, Valle TT, Tuomilehto J, Bergman RN, ... ... Collins FS, et al. Mitochondrial polymorphisms and susceptibility to type 2 diabetes-related traits in Finns. Human Genetics. 118: 245-54. PMID 16142453 DOI: 10.1007/S00439-005-0046-4  1
2005 Capell BC, Erdos MR, Madigan JP, Fiordalisi JJ, Varga R, Conneely KN, Gordon LB, Der CJ, Cox AD, Collins FS. Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome. Proceedings of the National Academy of Sciences of the United States of America. 102: 12879-84. PMID 16129833 DOI: 10.1073/Pnas.0506001102  1
2005 Adeyemo AA, Johnson T, Acheampong J, Oli J, Okafor G, Amoah A, Owusu S, Agyenim-Boateng K, Eghan BA, Abbiyesuku F, Fasanmade O, Rufus T, Doumatey A, Chen G, Zhou J, ... ... Collins F, et al. A genome wide quantitative trait linkage analysis for serum lipids in type 2 diabetes in an African population. Atherosclerosis. 181: 389-97. PMID 16039295 DOI: 10.1016/J.Atherosclerosis.2004.12.049  1
2005 Agarwal SK, Kennedy PA, Scacheri PC, Novotny EA, Hickman AB, Cerrato A, Rice TS, Moore JB, Rao S, Ji Y, Mateo C, Libutti SK, Oliver B, Chandrasekharappa SC, Burns AL, ... Collins FS, et al. Menin molecular interactions: insights into normal functions and tumorigenesis. Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et MéTabolisme. 37: 369-74. PMID 16001329 DOI: 10.1055/S-2005-870139  1
2005 Jenkins J, Grady PA, Collins FS. Nurses and the genomic revolution Journal of Nursing Scholarship. 37: 98-101. PMID 15960052 DOI: 10.1111/J.1547-5069.2005.00020.X  1
2005 Mohlke KL, Skol AD, Scott LJ, Valle TT, Bergman RN, Tuomilehto J, Boehnke M, Collins FS. Evaluation of SLC2A10 (GLUT10) as a candidate gene for type 2 diabetes and related traits in Finns. Molecular Genetics and Metabolism. 85: 323-7. PMID 15936967 DOI: 10.1016/J.Ymgme.2005.04.011  1
2005 Chen Y, Kittles R, Zhou J, Chen G, Adeyemo A, Panguluri RK, Chen W, Amoah A, Opoku V, Acheampong J, Agyenim-Boateng K, Eghan BA, Nyantaki A, Oli J, Okafor G, ... ... Collins FS, et al. Calpain-10 gene polymorphisms and type 2 diabetes in West Africans: the Africa America Diabetes Mellitus (AADM) Study. Annals of Epidemiology. 15: 153-9. PMID 15652721 DOI: 10.1016/J.Annepidem.2004.05.014  1
2005 Bonham VL, Warshauer-Baker E, Collins FS. Race and ethnicity in the genome era: The complexity of the constructs American Psychologist. 60: 9-15. PMID 15641917 DOI: 10.1037/0003-066X.60.1.9  1
2005 Chen G, Adeyemo AA, Johnson T, Zhou J, Amoah A, Owusu S, Acheampong J, Agyenim-Boateng K, Eghan BA, Oli J, Okafor G, Abbiyesuku F, Dunston GM, Chen Y, Collins F, et al. A genome-wide scan for quantitative trait loci linked to obesity phenotypes among West Africans International Journal of Obesity. 29: 255-259. PMID 15611782 DOI: 10.1038/Sj.Ijo.0802873  1
2004 Scacheri PC, Crabtree JS, Kennedy AL, Swain GP, Ward JM, Marx SJ, Spiegel AM, Collins FS. Homozygous loss of menin is well tolerated in liver, a tissue not affected in MEN1. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 15: 872-7. PMID 15672591 DOI: 10.1007/S00335-004-2395-Z  1
2004 Guttmacher AE, Collins FS, Carmona RH. The family history - More important than ever New England Journal of Medicine. 351: 2333-2336. PMID 15564550 DOI: 10.1056/Nejmsb042979  1
2004 Austin CP, Brady LS, Insel TR, Collins FS. NIH Molecular Libraries Initiative. Science (New York, N.Y.). 306: 1138-9. PMID 15542455 DOI: 10.1126/Science.1105511  1
2004 Conneely KN, Silander K, Scott LJ, Mohlke KL, Lazaridis KN, Valle TT, Tuomilehto J, Bergman RN, Watanabe RM, Buchanan TA, Collins FS, Boehnke M. Variation in the resistin gene is associated with obesity and insulin-related phenotypes in Finnish subjects. Diabetologia. 47: 1782-8. PMID 15517149 DOI: 10.1007/S00125-004-1537-X  1
2004 Collins FS. What we do and don't know about 'race', 'ethnicity', genetics and health at the dawn of the genome era Nature Genetics. 36. PMID 15507997 DOI: 10.1038/Ng1436  1
2004 Feingold EA, Good PJ, Guyer MS, Kamholz S, Liefer L, Wetterstrand K, Collins FS, Gingeras TR, Kampa D, Sekinger EA, Cheng J, Hirsch H, Ghosh S, Zhu Z, Patel S, et al. The ENCODE (ENCyclopedia of DNA Elements) Project Science. 306: 636-640. PMID 15499007 DOI: 10.1126/Science.1105136  1
2004 Gerhard DS, Wagner L, Feingold EA, Shenmen CM, Grouse LH, Schuler G, Klein SL, Old S, Rasooly R, Good P, Guyer M, Peck AM, Derge JG, Lipman D, Collins FS, et al. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). Genome Research. 14: 2121-7. PMID 15489334 DOI: 10.1101/Gr.2596504  1
2004 Scacheri PC, Kennedy AL, Chin K, Miller MT, Hodgson JG, Gray JW, Marx SJ, Spiegel AM, Collins FS. Pancreatic insulinomas in multiple endocrine neoplasia, type I knockout mice can develop in the absence of chromosome instability or microsatellite instability. Cancer Research. 64: 7039-44. PMID 15466197 DOI: 10.1158/0008-5472.Can-04-1648  1
2004 Austin CP, Battey JF, Bradley A, Bucan M, Capecchi M, Collins FS, Dove WF, Duyk G, Dymecki S, Eppig JT, Grieder FB, Heintz N, Hicks G, Insel TR, Joyner A, et al. The knockout mouse project. Nature Genetics. 36: 921-4. PMID 15340423 DOI: 10.1038/Ng0904-921  1
2004 Collins FS. An audience with...Francis S. Collins [interview] Nature Reviews. Drug Discovery. 3: 640. PMID 15317147 DOI: 10.1038/Nrd1488  1
2004 Lipkin SM, Rozek LS, Rennert G, Yang W, Chen PC, Hacia J, Hunt N, Shin B, Fodor S, Kokoris M, Greenson JK, Fearon E, Lynch H, Collins F, Gruber SB. The MLH1 D132H variant is associated with susceptibility to sporadic colorectal cancer. Nature Genetics. 36: 694-9. PMID 15184898 DOI: 10.1038/Ng1374  1
2004 Goldman RD, Shumaker DK, Erdos MR, Eriksson M, Goldman AE, Gordon LB, Gruenbaum Y, Khuon S, Mendez M, Varga R, Collins FS. Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome. Proceedings of the National Academy of Sciences of the United States of America. 101: 8963-8. PMID 15184648 DOI: 10.1073/Pnas.0402943101  1
2004 Ahaghotu C, Baffoe-Bonnie A, Kittles R, Pettaway C, Powell I, Royal C, Wang H, Vijayakumar S, Bennett J, Hoke G, Mason T, Bailey-Wilson J, Boykin W, Berg K, Carpten J, ... ... Collins F, et al. Clinical characteristics of African-American men with heriditary prostate cancer: The AAHPC study Prostate Cancer and Prostatic Diseases. 7: 165-169. PMID 15175665 DOI: 10.1038/Sj.Pcan.4500719  1
2004 Collins FS. The case for a US prospective cohort study of genes and environment Nature. 429: 475-477. PMID 15164074 DOI: 10.1038/Nature02628  1
2004 Agarwal SK, Lee Burns A, Sukhodolets KE, Kennedy PA, Obungu VH, Hickman AB, Mullendore ME, Whitten I, Skarulis MC, Simonds WF, Mateo C, Crabtree JS, Scacheri PC, Ji Y, Novotny EA, ... ... Collins FS, et al. Molecular pathology of the MEN1 gene. Annals of the New York Academy of Sciences. 1014: 189-98. PMID 15153434 DOI: 10.1196/Annals.1294.020  1
2004 Silander K, Mohlke KL, Scott LJ, Peck EC, Hollstein P, Skol AD, Jackson AU, Deloukas P, Hunt S, Stavrides G, Chines PS, Erdos MR, Narisu N, Conneely KN, Li C, ... ... Collins FS, et al. Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes. Diabetes. 53: 1141-9. PMID 15047633 DOI: 10.2337/Diabetes.53.4.1141  1
2004 Rotimi CN, Chen G, Adeyemo AA, Furbert-Harris P, Parish-Gause D, Zhou J, Berg K, Adegoke O, Amoah A, Owusu S, Acheampong J, Agyenim-Boateng K, Eghan BA, Oli J, Okafor G, ... ... Collins FS, et al. A genome-wide search for type 2 diabetes susceptibility genes in West Africans: the Africa America Diabetes Mellitus (AADM) Study. Diabetes. 53: 838-41. PMID 14988271 DOI: 10.2337/Diabetes.53.3.838  1
2004 Silander K, Scott LJ, Valle TT, Mohlke KL, Stringham HM, Wiles KR, Duren WL, Doheny KF, Pugh EW, Chines P, Narisu N, White PP, Fingerlin TE, Jackson AU, Li C, ... ... Collins FS, et al. A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14. Diabetes. 53: 821-9. PMID 14988269 DOI: 10.2337/Diabetes.53.3.821  1
2004 Scacheri PC, Rozenblatt-Rosen O, Caplen NJ, Wolfsberg TG, Umayam L, Lee JC, Hughes CM, Shanmugam KS, Bhattacharjee A, Meyerson M, Collins FS. Short interfering RNAs can induce unexpected and divergent changes in the levels of untargeted proteins in mammalian cells. Proceedings of the National Academy of Sciences of the United States of America. 101: 1892-7. PMID 14769924 DOI: 10.1073/Pnas.0308698100  1
2004 Collins FS. Francis S. Collins Nature Reviews Drug Discovery. 3: 640.  1
2003 Collins FS. Genome research: The next generation Cold Spring Harbor Symposia On Quantitative Biology. 68: 49-54. PMID 15338602 DOI: 10.1101/Sqb.2003.68.49  1
2003 Collins FS. An interview with Francis S. Collins, M.D., Ph.D. Director, National Human Genome Research Institute Assay Drug Dev Technol. 1: 119-125. PMID 15090138  1
2003 Albin RL. Genomic medicine. The New England Journal of Medicine. 349: 2170-1; author reply. PMID 14645650 DOI: 10.1056/Nejm200311273492219  1
2003 Collins FS, Watson JD. Genetic discrimination: time to act. Science (New York, N.Y.). 302: 745. PMID 14593134 DOI: 10.1126/Science.302.5646.745  1
2003 Baxevanis AD, Collins FS. Power to the people. A User's Guide to the Human Genome. Foreward Nature Genetics. 35: 2. PMID 14578888 DOI: 10.1038/Ng1185  1
2003 Agarwal SK, Novotny EA, Crabtree JS, Weitzman JB, Yaniv M, Burns AL, Chandrasekharappa SC, Collins FS, Spiegel AM, Marx SJ. Transcription factor JunD, deprived of menin, switches from growth suppressor to growth promoter. Proceedings of the National Academy of Sciences of the United States of America. 100: 10770-5. PMID 12960363 DOI: 10.1073/Pnas.1834524100  1
2003 Guttmacher AE, Collins FS. Welcome to the genomic era New England Journal of Medicine. 349: 996-998. PMID 12954750 DOI: 10.1056/Nejme038132  1
2003 Crabtree JS, Scacheri PC, Ward JM, McNally SR, Swain GP, Montagna C, Hager JH, Hanahan D, Edlund H, Magnuson MA, Garrett-Beal L, Burns AL, Ried T, Chandrasekharappa SC, Marx SJ, ... ... Collins FS, et al. Of mice and MEN1: Insulinomas in a conditional mouse knockout. Molecular and Cellular Biology. 23: 6075-85. PMID 12917331 DOI: 10.1128/Mcb.23.17.6075-6085.2003  1
2003 Patenaude AF, Guttmacher AE, Collins FS. Psychologists' Contributions to the Genetic Revolution American Psychologist. 58: 319-320. PMID 12866400 DOI: 10.1037/0003-066X.58.4.319B  1
2003 Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, Erdos MR, Robbins CM, Moses TY, Berglund P, Dutra A, Pak E, Durkin S, Csoka AB, Boehnke M, ... ... Collins FS, et al. Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome. Nature. 423: 293-8. PMID 12714972 DOI: 10.1038/Nature01629  1
2003 Collins FS, Green ED, Guttmacher AE, Guyer MS. A vision for the future of genomics research Nature. 422: 835-847. PMID 12695777 DOI: 10.1038/Nature01626  1
2003 Collins FS, Morgan M, Patrinos A. The Human Genome Project: Lessons from large-scale biology Science. 300: 286-290. PMID 12690187 DOI: 10.1126/Science.1084564  1
2003 Insel TR, Collins FS. Psychiatry in the genomics era. The American Journal of Psychiatry. 160: 616-20. PMID 12668345 DOI: 10.1176/Appi.Ajp.160.4.616  1
2003 Grady PA, Collins FS. Genetics and nursing science: realizing the potential Nursing Research. 52: 69. PMID 12657981 DOI: 10.1097/00006199-200303000-00001  1
2003 Sukhodolets KE, Hickman AB, Agarwal SK, Sukhodolets MV, Obungu VH, Novotny EA, Crabtree JS, Chandrasekharappa SC, Collins FS, Spiegel AM, Burns AL, Marx SJ. The 32-kilodalton subunit of replication protein A interacts with menin, the product of the MEN1 tumor suppressor gene. Molecular and Cellular Biology. 23: 493-509. PMID 12509449 DOI: 10.1128/Mcb.23.2.493-509.2003  1
2003 Olopade OI, Fackenthal JD, Dunston G, Tainsky MA, Collins F, Whitfield-Broome C. Breast cancer genetics in African Americans. Cancer. 97: 236-45. PMID 12491487 DOI: 10.1002/Cncr.11019  1
2003 Belmont JW, Hardenbol P, Willis TD, Yu F, Yang H, Ch'Ang LY, Huang W, Liu B, Shen Y, Tam PKH, Tsui LC, Waye MMY, Wong JTF, Zeng C, Zhang Q, ... ... Collins FS, et al. The international HapMap project Nature. 426: 789-796. DOI: 10.1038/Nature02168  1
2002 Mohlke KL, Erdos MR, Scott LJ, Fingerlin TE, Jackson AU, Silander K, Hollstein P, Boehnke M, Collins FS. High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools. Proceedings of the National Academy of Sciences of the United States of America. 99: 16928-33. PMID 12482934 DOI: 10.1073/Pnas.262661399  1
2002 Strausberg RL, Feingold EA, Grouse LH, Derge JG, Klausner RD, Collins FS, Wagner L, Shenmen CM, Schuler GD, Altschul SF, Zeeberg B, Buetow KH, Schaefer CF, Bhat NK, Hopkins RF, et al. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Proceedings of the National Academy of Sciences of the United States of America. 99: 16899-903. PMID 12477932 DOI: 10.1073/Pnas.242603899  1
2002 Waterston RH, Lindblad-Toh K, Birney E, Rogers J, Abril JF, Agarwal P, Agarwala R, Ainscough R, Alexandersson M, An P, Antonarakis SE, Attwood J, Baertsch R, Bailey J, ... ... Collins FS, et al. Initial sequencing and comparative analysis of the mouse genome. Nature. 420: 520-62. PMID 12466850 DOI: 10.1038/Nature01262  1
2002 Guttmacher AE, Collins FS. Genomic medicine - A primer New England Journal of Medicine. 347: 1512-1520. PMID 12421895 DOI: 10.1056/Nejmra012240  1
2002 Mykytyn K, Nishimura DY, Searby CC, Shastri M, Yen HJ, Beck JS, Braun T, Streb LM, Cornier AS, Cox GF, Fulton AB, Carmi R, Lüleci G, Chandrasekharappa SC, Collins FS, et al. Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome. Nature Genetics. 31: 435-8. PMID 12118255 DOI: 10.1038/Ng935  1
2002 Lipkin SM, Moens PB, Wang V, Lenzi M, Shanmugarajah D, Gilgeous A, Thomas J, Cheng J, Touchman JW, Green ED, Schwartzberg P, Collins FS, Cohen PE. Meiotic arrest and aneuploidy in MLH3-deficient mice Nature Genetics. 31: 385-390. PMID 12091911 DOI: 10.1038/Ng931  1
2002 Fingerlin TE, Erdos MR, Watanabe RM, Wiles KR, Stringham HM, Mohlke KL, Silander K, Valle TT, Buchanan TA, Tuomilehto J, Bergman RN, Boehnke M, Collins FS. Variation in three single nucleotide polymorphisms in the calpain-10 gene not associated with type 2 diabetes in a large Finnish cohort. Diabetes. 51: 1644-8. PMID 11978669 DOI: 10.2337/Diabetes.51.5.1644  1
2002 Patenaude AF, Guttmacher AE, Collins FS. Genetic testing and psychology: New roles, new responsibilities American Psychologist. 57: 271-282. PMID 11975377 DOI: 10.1037/0003-066X.57.4.271  1
2002 Guttmacher AE, Collins FS, Burke W. Genomic medicine: Genetic testing New England Journal of Medicine. 347: 1867-1875. DOI: 10.1056/NEJMoa012113  1
2002 Baxevanis AD, Collins FS. Power to the people Nature Genetics. 32: 2. DOI: 10.1038/ng962  1
2001 Collins FS, Guttmacher AE. Genetics moves into the medical mainstream Journal of the American Medical Association. 286: 2322-2324. PMID 11710899 DOI: 10.1001/Jama.286.18.2322  1
2001 Scacheri PC, Crabtree JS, Novotny EA, Garrett-Beal L, Chen A, Edgemon KA, Marx SJ, Spiegel AM, Chandrasekharappa SC, Collins FS. Bidirectional transcriptional activity of PGK-neomycin and unexpected embryonic lethality in heterozygote chimeric knockout mice. Genesis (New York, N.Y. : 2000). 30: 259-63. PMID 11536432 DOI: 10.1002/Gene.1072  1
2001 Heppner C, Bilimoria KY, Agarwal SK, Kester M, Whitty LJ, Guru SC, Chandrasekharappa SC, Collins FS, Spiegel AM, Marx SJ, Burns AL. The tumor suppressor protein menin interacts with NF-kappaB proteins and inhibits NF-kappaB-mediated transactivation. Oncogene. 20: 4917-25. PMID 11526476 DOI: 10.1038/Sj.Onc.1204529  1
2001 Mohlke KL, Lange EM, Valle TT, Ghosh S, Magnuson VL, Silander K, Watanabe RM, Chines PS, Bergman RN, Tuomilehto J, Collins FS, Boehnke M. Linkage disequilibrium between microsatellite markers extends beyond 1 cM on chromosome 20 in Finns. Genome Research. 11: 1221-6. PMID 11435404 DOI: 10.1101/Gr.173201  1
2001 Collins FS. Contemplating the end of the beginning Genome Research. 11: 641-643. PMID 11337461 DOI: 10.1101/Gr.1898  1
2001 Lipkin SM, Wang V, Stoler DL, Anderson GR, Kirsch I, Hadley D, Lynch HT, Collins FS. Germline and somatic mutation analyses in the DNA mismatch repair gene MLH3: Evidence for somatic mutation in colorectal cancers Human Mutation. 17: 389-396. PMID 11317354 DOI: 10.1002/Humu.1114  1
2001 Douglas JA, Erdos MR, Watanabe RM, Braun A, Johnston CL, Oeth P, Mohlke KL, Valle TT, Ehnholm C, Buchanan TA, Bergman RN, Collins FS, Boehnke M, Tuomilehto J. The peroxisome proliferator-activated receptor-gamma2 Pro12A1a variant: association with type 2 diabetes and trait differences. Diabetes. 50: 886-90. PMID 11289057 DOI: 10.2337/Diabetes.50.4.886  1
2001 Guru SC, Prasad NB, Shin EJ, Hemavathy K, Lu J, Ip YT, Agarwal SK, Marx SJ, Spiegel AM, Collins FS, Oliver B, Chandrasekharappa SC. Characterization of a MEN1 ortholog from Drosophila melanogaster. Gene. 263: 31-8. PMID 11223240 DOI: 10.1016/S0378-1119(00)00562-X  1
2001 Collins FS, McKusick VA. Implications of the Human Genome Project for medical science. Jama. 285: 540-4. PMID 11176855 DOI: 10.1001/Jama.285.5.540  1
2001 Rotimi CN, Dunston GM, Berg K, Akinsete O, Amoah A, Owusu S, Acheampong J, Boateng K, Oli J, Okafor G, Onyenekwe B, Osotimehin B, Abbiyesuku F, Johnson T, Fasanmade O, ... ... Collins F, et al. In search of susceptibility genes for type 2 diabetes in West Africa: The design and results of the first phase of the AADM study Annals of Epidemiology. 11: 51-58. PMID 11164120 DOI: 10.1016/S1047-2797(00)00180-0  1
2001 Crabtree JS, Scacheri PC, Ward JM, Garrett-Beal L, Emmert-Buck MR, Edgemon KA, Lorang D, Libutti SK, Chandrasekharappa SC, Marx SJ, Spiegel AM, Collins FS. A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors. Proceedings of the National Academy of Sciences of the United States of America. 98: 1118-23. PMID 11158604 DOI: 10.1073/Pnas.98.3.1118  1
2001 Collins FS, Mansoura MK. The human genome project: Revealing the shared inheritance of all humankind Cancer. 91: 221-225. PMID 11148583 DOI: 10.1002/1097-0142(20010101)91:1+<221::Aid-Cncr8>3.3.Co;2-0  1
2000 Royal C, Baffoe-Bonnie A, Kittles R, Powell I, Bennett J, Hoke G, Pettaway C, Weinrich S, Vijayakumar S, Ahaghotu C, Mason T, Johnson E, Obeikwe M, Simpson C, Mejia R, ... ... Collins F, et al. Recruitment experience in the first phase of the African American Hereditary Prostate Cancer (AAHPC) study Annals of Epidemiology. 10. PMID 11189095 DOI: 10.1016/S1047-2797(00)00194-0  1
2000 Knapp JI, Heppner C, Hickman AB, Burns AL, Chandrasekharappa SC, Collins FS, Marx SJ, Spiegel AM, Agarwal SK. Identification and characterization of JunD missense mutants that lack menin binding. Oncogene. 19: 4706-12. PMID 11032020 DOI: 10.1038/Sj.Onc.1203832  1
2000 Karanjawala ZE, Kääriäinen H, Ghosh S, Tannenbaum J, Martin C, Ally D, Tuomilehto J, Valle T, Collins FS. Complete maternal isodisomy of chromosome 8 in an individual with an early-onset ileal carcinoid tumor. American Journal of Medical Genetics. 93: 207-10. PMID 10925383 DOI: 10.1002/1096-8628(20000731)93:3<207::Aid-Ajmg9>3.0.Co;2-A  1
2000 Manickam P, Vogel AM, Agarwal SK, Oda T, Spiegel AM, Marx SJ, Collins FS, Weinstein BM, Chandrasekharappa SC. Isolation, characterization, expression and functional analysis of the zebrafish ortholog of MEN1. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 11: 448-54. PMID 10818209 DOI: 10.1007/S003350010085  1
2000 Debelenko LV, Swalwell JI, Kelley MJ, Brambilla E, Manickam P, Baibakov G, Agarwal SK, Spiegel AM, Marx SJ, Chandrasekharappa SC, Collins FS, Travis WD, Emmert-Buck MR. MEN1 gene mutation analysis of high-grade neuroendocrine lung carcinoma. Genes, Chromosomes & Cancer. 28: 58-65. PMID 10738303 DOI: 10.1002/(Sici)1098-2264(200005)28:1<58::Aid-Gcc7>3.0.Co;2-2  1
2000 Guttmacher AE, Collins FS. Genetics resources on the Web (GROW) Genetics in Medicine. 2: 296-299. DOI: 10.1097/00125817-200009000-00005  1
1999 Collins FS, Jegalian KG. Deciphering the Code of Life Scientific American. 281: 86-91. PMID 10614070 DOI: 10.1038/Scientificamerican1299-86  1
1999 Kim YS, Burns AL, Goldsmith PK, Heppner C, Park SY, Chandrasekharappa SC, Collins FS, Spiegel AM, Marx SJ. Stable overexpression of MEN1 suppresses tumorigenicity of RAS. Oncogene. 18: 5936-42. PMID 10557080 DOI: 10.1038/Sj.Onc.1203005  1
1999 Hacia JG, Collins FS. Mutational analysis using oligonucleotide microarrays Journal of Medical Genetics. 36: 730-736. PMID 10528850 DOI: 10.1136/Jmg.36.10.730  1
1999 Strausberg RL, Feingold EA, Klausner RD, Collins FS. The mammalian gene collection. Science (New York, N.Y.). 286: 455-7. PMID 10521335 DOI: 10.1126/Science.286.5439.455  1
1999 Marx SJ, Agarwal SK, Heppner C, Kim YS, Kester MB, Goldsmith PK, Skarulis MC, Spiegel AM, Burns AL, Debelenko LV, Zhuang Z, Lubensky IA, Liotta LA, Emmert-Buck MR, Guru SC, ... ... Collins FS, et al. The gene for multiple endocrine neoplasia type 1: recent findings. Bone. 25: 119-22. PMID 10423035 DOI: 10.1016/S8756-3282(99)00112-X  1
1999 Collins FS. The Human Genome Project and the future of medicine Annals of the New York Academy of Sciences. 882: 42-55. PMID 10415885 DOI: 10.1111/J.1749-6632.1999.Tb08532.X  1
1999 Collins FS. Shattuck lecture - Medical and societal consequences of the human genome project New England Journal of Medicine. 341: 28-37. PMID 10387940 DOI: 10.1056/Nejm199907013410106  1
1999 Hacia JG, Fan JB, Ryder O, Jin L, Edgemon K, Ghandour G, Mayer RA, Sun B, Hsie L, Robbins CM, Brody LC, Wang D, Lander ES, Lipshutz R, Fodor SP, ... Collins FS, et al. Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays. Nature Genetics. 22: 164-7. PMID 10369258 DOI: 10.1038/9674  1
1999 Watanabe RM, Valle T, Hauser ER, Ghosh S, Eriksson J, Kohtamäki K, Ehnholm C, Tuomilehto J, Collins FS, Bergman RN, Boehnke M. Familiality of quantitative metabolic traits in Finnish families with non-insulin-dependent diabetes mellitus. Finland-United States Investigation of NIDDM Genetics (FUSION) Study investigators. Human Heredity. 49: 159-68. PMID 10364681 DOI: 10.1159/000022865  1
1999 Guru SC, Crabtree JS, Brown KD, Dunn KJ, Manickam P, Prasad NB, Wangsa D, Burns AL, Spiegel AM, Marx SJ, Pavan WJ, Collins FS, Chandrasekharappa SC. Isolation, genomic organization, and expression analysis of Men1, the murine homolog of the MEN1 gene. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 10: 592-6. PMID 10341092 DOI: 10.1007/S003359901051  1
1999 Ghosh S, Langefeld CD, Ally D, Watanabe RM, Hauser ER, Magnuson VL, Nylund SJ, Valle T, Eriksson J, Bergman RN, Tuomilehto J, Collins FS, Boehnke M. The W64R variant of the beta3-adrenergic receptor is not associated with type II diabetes or obesity in a large Finnish sample. Diabetologia. 42: 238-44. PMID 10064105 DOI: 10.1007/S001250051144  1
1999 Ghosh S, Watanabe RM, Hauser ER, Valle T, Magnuson VL, Erdos MR, Langefeld CD, Balow J, Ally DS, Kohtamaki K, Chines P, Birznieks G, Kaleta HS, Musick A, Te C, ... ... Collins FS, et al. Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs. Proceedings of the National Academy of Sciences of the United States of America. 96: 2198-203. PMID 10051618 DOI: 10.1073/Pnas.96.5.2198  1
1999 Agarwal SK, Guru SC, Heppner C, Erdos MR, Collins RM, Park SY, Saggar S, Chandrasekharappa SC, Collins FS, Spiegel AM, Marx SJ, Burns AL. Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription. Cell. 96: 143-52. PMID 9989505 DOI: 10.1016/S0092-8674(00)80967-8  1
1999 Collins FS. Genetics: An explosion of knowledge is transforming clinical practice Geriatrics. 54: 41-47. PMID 9934355  1
1999 Collins FS, Bochm K. Avoiding casualties in the genetic revolution: The urgent need to educate physicians about genetics Academic Medicine. 74: 48-49. PMID 9934295  1
1999 Collins FS. Microarrays and macroconsequences Nature Genetics. 21: 2-2. DOI: 10.1038/4425  1
1998 Krkljus S, Abernathy CR, Johnson JS, Williams CA, Driscoll DJ, Zori R, Stalker HJ, Rasmussen SA, Collins FS, Kousseff BG, Baumbach L, Wallace MR. Analysis of CpG C-to-T mutations in neurofibromatosis type 1. Mutations in brief no. 129. Online. Human Mutation. 11: 411. PMID 10336779 DOI: 10.1002/(Sici)1098-1004(1998)11:5<411::Aid-Humu11>3.0.Co;2-2  1
1998 Collins FS, Brooks LD, Chakravarti A. A DNA polymorphism discovery resource for research on human genetic variation Genome Research. 8: 1229-1231. PMID 9872978 DOI: 10.1101/Gr.8.12.1229  1
1998 Hacia JG, Brody LC, Collins FS. Applications of DNA chips for genomic analysis Molecular Psychiatry. 3: 483-492. PMID 9857973 DOI: 10.1038/Sj.Mp.4000475  1
1998 Centola M, Chen X, Sood R, Deng Z, Aksentijevich I, Blake T, Ricke DO, Chen X, Wood G, Zaks N, Richards N, Krizman D, Mansfield E, Apostolou S, Liu J, ... ... Collins FS, et al. Construction of an approximately 700-kb transcript map around the familial Mediterranean fever locus on human chromosome 16p13.3. Genome Research. 8: 1172-91. PMID 9847080 DOI: 10.1101/Gr.8.11.1172  1
1998 Karanjawala ZE, Collins FS. Genetics in the context of medical practice Journal of the American Medical Association. 280: 1533-1534. PMID 9809738 DOI: 10.1001/Jama.280.17.1533-Jms1104-3-1  1
1998 Xu J, Meyers D, Freije D, Isaacs S, Wiley K, Nusskern D, Ewing C, Wilkens E, Bujnovszky P, Bova GS, Walsh P, Isaacs W, Schleutker J, Matikainen M, Tammela T, ... ... Collins F, et al. Evidence for a prostate cancer susceptibility locus on the X chromosome. Nature Genetics. 20: 175-9. PMID 9771711 DOI: 10.1016/S0022-5347(01)61689-6  1
1998 Marx S, Spiegel AM, Skarulis MC, Doppman JL, Collins FS, Liotta LA. Multiple endocrine neoplasia type 1: clinical and genetic topics. Annals of Internal Medicine. 129: 484-94. PMID 9735087 DOI: 10.7326/0003-4819-129-6-199809150-00011  1
1998 Ghosh S, Hauser ER, Magnuson VL, Valle T, Ally DS, Karanjawala ZE, Rayman JB, Knapp JI, Musick A, Tannenbaum J, Te C, Eldridge W, Shapiro S, Musick T, Martin C, et al. A large sample of finnish diabetic sib-pairs reveals no evidence for a non-insulin-dependent diabetes mellitus susceptibility locus at 2qter. The Journal of Clinical Investigation. 102: 704-9. PMID 9710438 DOI: 10.1172/Jci2512  1
1998 Marx SJ, Agarwal SK, Kester MB, Heppner C, Kim YS, Emmert-Buck MR, Debelenko LV, Lubensky IA, Zhuang Z, Guru SC, Manickam P, Olufemi SE, Skarulis MC, Doppman JL, Alexander RH, ... ... Collins FS, et al. Germline and somatic mutation of the gene for multiple endocrine neoplasia type 1 (MEN1). Journal of Internal Medicine. 243: 447-53. PMID 9681842 DOI: 10.1046/J.1365-2796.1998.00348.X  1
1998 Agarwal SK, Debelenko LV, Kester MB, Guru SC, Manickam P, Olufemi SE, Skarulis MC, Heppner C, Crabtree JS, Lubensky IA, Zhuang Z, Kim YS, Chandrasekharappa SC, Collins FS, Liotta LA, et al. Analysis of recurrent germline mutations in the MEN1 gene encountered in apparently unrelated families. Human Mutation. 12: 75-82. PMID 9671267 DOI: 10.1002/(Sici)1098-1004(1998)12:2<75::Aid-Humu1>3.0.Co;2-T  1
1998 Burke W, Thomson E, Khoury MJ, McDonnell SM, Press N, Adams PC, Barton JC, Beutler E, Brittenham G, Buchanan A, Clayton EW, Cogswell ME, Meslin EM, Motulsky AG, Powell LW, ... ... Collins FS, et al. Hereditary hemochromatosis: gene discovery and its implications for population-based screening. Jama. 280: 172-8. PMID 9669792 DOI: 10.1001/Jama.280.2.172  1
1998 Valle T, Tuomilehto J, Bergman RN, Ghosh S, Hauser ER, Eriksson J, Nylund SJ, Kohtamäki K, Toivanen L, Vidgren G, Tuomilehto-Wolf E, Ehnholm C, Blaschak J, Langefeld CD, Watanabe RM, ... ... Collins F, et al. Mapping genes for NIDDM. Design of the Finland-United States Investigation of NIDDM Genetics (FUSION) Study. Diabetes Care. 21: 949-58. PMID 9614613 DOI: 10.2337/Diacare.21.6.949  1
1998 Emmert-Buck MR, Debelenko LV, Agarwal S, Kester MB, Manickam P, Zhuang Z, Guru SC, Olufemi SE, Burns AL, Chandrasekharappa SC, Lubensky IA, Liotta LA, Skarulis MC, Spiegel AM, Marx SJ, ... Collins FS, et al. 11q13 allelotype analysis in 27 northern American MEN1 kindreds identifies two distinct founder chromosomes. Molecular Genetics and Metabolism. 63: 151-5. PMID 9562970 DOI: 10.1006/Mgme.1997.2649  1
1998 Olufemi SE, Green JS, Manickam P, Guru SC, Agarwal SK, Kester MB, Dong Q, Burns AL, Spiegel AM, Marx SJ, Collins FS, Chandrasekharappa SC. Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1Burin) in four kindreds from Newfoundland. Human Mutation. 11: 264-9. PMID 9554741 DOI: 10.1002/(Sici)1098-1004(1998)11:4<264::Aid-Humu2>3.0.Co;2-V  1
1998 Guru SC, Goldsmith PK, Burns AL, Marx SJ, Spiegel AM, Collins FS, Chandrasekharappa SC. Menin, the product of the MEN1 gene, is a nuclear protein. Proceedings of the National Academy of Sciences of the United States of America. 95: 1630-4. PMID 9465067 DOI: 10.1073/Pnas.95.4.1630  1
1998 Hacia JG, Makalowski W, Edgemon K, Erdos MR, Robbins CM, Fodor SP, Brody LC, Collins FS. Evolutionary sequence comparisons using high-density oligonucleotide arrays. Nature Genetics. 18: 155-8. PMID 9462745 DOI: 10.1038/Ng0298-155  1
1998 Hacia JG, Brody LC, Collins FS. New approaches to BRCA1 mutation detection Breast Disease. 10: 45-59. DOI: 10.3233/Bd-1998-101-207  1
1997 Kahn MJ, Jamison KR, Collins FS. Protecting our 'family secrets' The Washington Post. A15. PMID 11647280  1
1997 Collins FS, Guyer MS, Chakravarti A. Variations on a theme: Cataloging human DNA sequence variation Science. 278: 1580-1581. PMID 9411782 DOI: 10.1126/Science.278.5343.1580  1
1997 Manickam P, Guru SC, Debelenko LV, Agarwal SK, Olufemi SE, Weisemann JM, Boguski MS, Crabtree JS, Wang Y, Roe BA, Lubensky IA, Zhuang Z, Kester MB, Burns AL, Spiegel AM, ... ... Collins FS, et al. Eighteen new polymorphic markers in the multiple endocrine neoplasia type 1 (MEN1) region. Human Genetics. 101: 102-8. PMID 9385379 DOI: 10.1007/s004390050595  1
1997 Debelenko LV, Brambilla E, Agarwal SK, Swalwell JI, Kester MB, Lubensky IA, Zhuang Z, Guru SC, Manickam P, Olufemi SE, Chandrasekharappa SC, Crabtree JS, Kim YS, Heppner C, Burns AL, ... ... Collins FS, et al. Identification of MEN1 gene mutations in sporadic carcinoid tumors of the lung. Human Molecular Genetics. 6: 2285-90. PMID 9361035 DOI: 10.1093/Hmg/6.13.2285  1
1997 Collins FS. Preparing health professionals for the genetic revolution Journal of the American Medical Association. 278: 1285-1286. PMID 9333274 DOI: 10.1001/Jama.1997.03550150089043  1
1997 Woodage T, Basrai MA, Baxevanis AD, Hieter P, Collins FS. Characterization of the CHD family of proteins Proceedings of the National Academy of Sciences of the United States of America. 94: 11472-11477. PMID 9326634 DOI: 10.1073/Pnas.94.21.11472  1
1997 Balow JE, Shelton DA, Orsborn A, Mangelsdorf M, Aksentijevich I, Blake T, Sood R, Gardner D, Liu R, Pras E, Levy EN, Centola M, Deng Z, Zaks N, Wood G, ... ... Collins FS, et al. A high-resolution genetic map of the familial Mediterranean fever candidate region allows identification of haplotype-sharing among ethnic groups. Genomics. 44: 280-91. PMID 9325049 DOI: 10.1006/Geno.1997.4860  1
1997 Aksentijevich I, Centola M, Deng Z, Sood R, Balow J.E. J, Wood G, Zaks N, Mansfield E, Chen X, Eisenberg S, Vedula A, Shafran N, Raben N, Pras E, Pras M, ... ... Collins FS, et al. Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever Cell. 90: 797-807. PMID 9288758 DOI: 10.1016/S0092-8674(00)80539-5  1
1997 Guru SC, Agarwal SK, Manickam P, Olufemi SE, Crabtree JS, Weisemann JM, Kester MB, Kim YS, Wang Y, Emmert-Buck MR, Liotta LA, Spiegel AM, Boguski MS, Roe BA, Collins FS, et al. A transcript map for the 2.8-Mb region containing the multiple endocrine neoplasia type 1 locus. Genome Research. 7: 725-35. PMID 9253601 DOI: 10.1101/Gr.7.7.725  1
1997 Heppner C, Kester MB, Agarwal SK, Debelenko LV, Emmert-Buck MR, Guru SC, Manickam P, Olufemi SE, Skarulis MC, Doppman JL, Alexander RH, Kim YS, Saggar SK, Lubensky IA, Zhuang Z, ... ... Collins FS, et al. Somatic mutation of the MEN1 gene in parathyroid tumours. Nature Genetics. 16: 375-8. PMID 9241276 DOI: 10.1038/ng0897-375  1
1997 Agarwal SK, Kester MB, Debelenko LV, Heppner C, Emmert-Buck MR, Skarulis MC, Doppman JL, Kim YS, Lubensky IA, Zhuang Z, Green JS, Guru SC, Manickam P, Olufemi SE, Liotta LA, ... ... Collins FS, et al. Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states. Human Molecular Genetics. 6: 1169-75. PMID 9215689 DOI: 10.1093/Hmg/6.7.1169  1
1997 Guru SC, Olufemi SE, Manickam P, Cummings C, Gieser LM, Pike BL, Bittner ML, Jiang Y, Chinault AC, Nowak NJ, Brzozowska A, Crabtree JS, Wang Y, Roe BA, Weisemann JM, ... ... Collins FS, et al. A 2.8-Mb clone contig of the multiple endocrine neoplasia type 1 (MEN1) region at 11q13. Genomics. 42: 436-45. PMID 9205115 DOI: 10.1006/Geno.1997.4783  1
1997 Sood R, Blake T, Aksentijevich I, Wood G, Chen X, Gardner D, Shelton DA, Mangelsdorf M, Orsborn A, Pras E, Balow JE, Centola M, Deng Z, Zaks N, Chen X, et al. Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the familial Mediterranean fever locus (MEFV) on chromosome 16p 13.3. Genomics. 42: 83-95. PMID 9177779 DOI: 10.1006/Geno.1997.4629  1
1997 Humphrey JS, Salim A, Erdos MR, Collins FS, Brody LC, Klausner RD. Human BRCA1 inhibits growth in yeast: potential use in diagnostic testing. Proceedings of the National Academy of Sciences of the United States of America. 94: 5820-5. PMID 9159158 DOI: 10.1073/Pnas.94.11.5820  1
1997 Dong Q, Debelenko LV, Chandrasekharappa SC, Emmert-Buck MR, Zhuang Z, Guru SC, Manickam P, Skarulis M, Lubensky IA, Liotta LA, Collins FS, Marx SJ, Spiegel AM. Loss of heterozygosity at 11q13: analysis of pituitary tumors, lung carcinoids, lipomas, and other uncommon tumors in subjects with familial multiple endocrine neoplasia type 1. The Journal of Clinical Endocrinology and Metabolism. 82: 1416-20. PMID 9141526 DOI: 10.1210/Jcem.82.5.3944  1
1997 Rothenberg K, Fuller B, Rothstein M, Duster T, Kahn MJE, Cunningham R, Fine B, Hudson K, King MC, Murphy P, Swergold G, Collins F. Genetic information and the workplace: Legislative approaches and policy challenges Science. 275: 1755-1757. PMID 9122681 DOI: 10.1126/Science.275.5307.1755  1
1997 Chandrasekharappa SC, Guru SC, Manickam P, Olufemi SE, Collins FS, Emmert-Buck MR, Debelenko LV, Zhuang Z, Lubensky IA, Liotta LA, Crabtree JS, Wang Y, Roe BA, Weisemann J, Boguski MS, et al. Positional cloning of the gene for multiple endocrine neoplasia-type 1. Science (New York, N.Y.). 276: 404-7. PMID 9103196 DOI: 10.1126/Science.276.5311.404  1
1997 Highsmith WE, Burch LH, Zhou Z, Olsen JC, Strong TV, Smith T, Friedman KJ, Silverman LM, Boucher RC, Collins FS, Knowles MR. Identification of a splice site mutation (2789 +5 G > A) associated with small amounts of normal CFTR mRNA and mild cystic fibrosis. Human Mutation. 9: 332-8. PMID 9101293 DOI: 10.1002/(Sici)1098-1004(1997)9:4<332::Aid-Humu5>3.0.Co;2-7  1
1997 Brown KD, Ziv Y, Sadanandan SN, Chessa L, Collins FS, Shiloh Y, Tagle DA. The ataxia-telangiectasia gene product, a constitutively expressed nuclear protein that is not up-regulated following genome damage. Proceedings of the National Academy of Sciences of the United States of America. 94: 1840-5. PMID 9050866 DOI: 10.1073/Pnas.94.5.1840  1
1997 Ghosh S, Karanjawala ZE, Hauser ER, Ally D, Knapp JI, Rayman JB, Musick A, Tannenbaum J, Te C, Shapiro S, Eldridge W, Musick T, Martin C, Smith JR, Carpten JD, ... ... Collins FS, et al. Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. FUSION (Finland-U.S. Investigation of NIDDM Genetics) Study Group. Genome Research. 7: 165-78. PMID 9049634 DOI: 10.1101/Gr.7.2.165  1
1997 Fink L, Collins FS. The Human Genome Project: view from the National Institutes of Health Journal of the American Medical Women's Association (1972). 52. PMID 9033164  1
1997 Russell MW, Du Manoir S, Collins FS, Brody LC. Cloning of the human NADH: Ubiquinone oxidoreductase subunit B13: Localization to Chromosome 7q32 and identification of a pseudogene on 11p15 Mammalian Genome. 8: 60-61. PMID 9021153 DOI: 10.1007/S003359900350  1
1997 Collins FS. Sequencing the human genome Hospital Practice. 32. DOI: 10.1080/21548331.1997.11443403  1
1996 Burke W, Kahn MJ, Garber JE, Collins FS. "First do no harm" also applies to cancer susceptibility testing The Cancer Journal From Scientific American.. 2: 250-252. PMID 9166540  1
1996 Hajra A, Collins FS. Structure of the leukemia-associated human CBFB gene Genomics. 38: 107. PMID 9064279 DOI: 10.1016/0888-7543(95)80177-N  1
1996 Russell MWW, Du Manoir S, Munroe DJ, Collins FS, Brody LC. Chromosomal localization of 15 ion channel genes Somatic Cell and Molecular Genetics. 22: 425-431. PMID 9039851 DOI: 10.1007/Bf02369898  1
1996 Hacia JG, Brody LC, Chee MS, Fodor SPA, Collins FS. Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colour fluorescence analysis Nature Genetics. 14: 441-449. PMID 8944024 DOI: 10.1016/S0165-4608(97)90265-X  1
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, ... ... Collins FS, 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  1
1996 Smith JR, Freije D, Carpten JD, Grönberg H, Xu J, Isaacs SD, Brownstein MJ, Bova GS, Guo H, Bujnovszky P, Nusskern DR, Damber JE, Bergh A, Emanuelsson M, Kallioniemi OP, ... ... Collins FS, et al. Major susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide search. Science (New York, N.Y.). 274: 1371-4. PMID 8910276 DOI: 10.1126/Science.274.5291.1371  1
1996 Magnuson VL, Ally DS, Nylund SJ, Karanjawala ZE, Rayman JB, Knapp JI, Lowe AL, Ghosh S, Collins FS. Substrate nucleotide-determined non-templated addition of adenine by Taq DNA polymerase: implications for PCR-based genotyping and cloning. Biotechniques. 21: 700-9. PMID 8891224 DOI: 10.2144/96214Rr03  1
1996 Russell MW, Dick M, Collins FS, Brody LC. KVLQT1 mutations in three families with familial or sporadic long QT syndrome Human Molecular Genetics. 5: 1319-1324. PMID 8872472 DOI: 10.1093/Hmg/5.9.1319  1
1996 Nasr SZ, Strong TV, Mansoura MK, Dawson DC, Collins FS. Novel missense mutation (G314R) in a cystic fibrosis patient with hepatic failure. Human Mutation. 7: 151-4. PMID 8829633 DOI: 10.1002/(Sici)1098-1004(1996)7:2<151::Aid-Humu10>3.0.Co;2-1  1
1996 Liu PP, Wijmenga C, Hajra A, Blake TB, Kelley CA, Adelstein RS, Bagg A, Rector J, Cotelingam J, Willman CL, Collins FS. Identification of the chimeric protein product of the CBFB-MYH11 fusion gene in inv(16) leukemia cells. Genes, Chromosomes & Cancer. 16: 77-87. PMID 8818654 DOI: 10.1002/(Sici)1098-2264(199606)16:2<77::Aid-Gcc1>3.0.Co;2-#  1
1996 Ghosh S, Collins FS. The geneticist's approach to complex disease Annual Review of Medicine. 47: 333-353. PMID 8712786 DOI: 10.1146/Annurev.Med.47.1.333  1
1996 Russell MW, Munroe DJ, Bric E, Housman DE, Dietz-Band J, Riethman HC, Collins FS, Brody LC. A 500-kb physical map and contig from the Harvey ras-1 gene to the 11p telomere. Genomics. 35: 353-60. PMID 8661149 DOI: 10.1006/Geno.1996.0367  1
1996 Pecker I, Avraham KB, Gilbert DJ, Savitsky K, Rotman G, Harnik R, Fukao T, Schröck E, Hirotsune S, Tagle DA, Collins FS, Wynshaw-Boris A, Ried T, Copeland NG, Jenkins NA, et al. Identification and chromosomal localization of Atm, the mouse homolog of the ataxia-telangiectasia gene. Genomics. 35: 39-45. PMID 8661102 DOI: 10.1006/Geno.1996.0320  1
1996 Savitsky K, Ziv Y, Bar-Shira A, Gilad S, Tagle DA, Smith S, Uziel T, Sfez S, Nahmias J, Sartiel A, Eddy RL, Shows TB, Collins FS, Shiloh Y, Rotman G. A human gene (DDX10) encoding a putative DEAD-box RNA helicase at 11q22-q23. Genomics. 33: 199-206. PMID 8660968 DOI: 10.1006/Geno.1996.0184  1
1996 Feigenbaum L, Fujita K, Collins FS, Jay G. Repression of the NFL gene by tax may explain the development of neurofibromas in human T-lymphotropic virus type 1 transgenic mice Journal of Virology. 70: 3280-3285. PMID 8627811  1
1996 Bryan SS, Mitchell AL, Collins F, Miao W, Marshall M, Jove R. N-terminal sequences contained in the Src homology 2 and 3 domains of p120 GTPase-activating protein are required for full catalytic activity toward Ras Journal of Biological Chemistry. 271: 5195-5199. PMID 8617802 DOI: 10.1074/Jbc.271.9.5195  1
1996 Rosenblatt DS, Foulkes WD, Narod SA, Collins FS. Genetic screening for breast cancer [3] New England Journal of Medicine. 334: 1200-1201. PMID 8602200 DOI: 10.1056/NEJM199605023341815  1
1996 Jordan E, Collins FS. A march of genetic maps Nature. 380: 111-112. PMID 8600381 DOI: 10.1038/380111A0  1
1996 Hajra A, Liu PP, Collins FS. Transforming properties of the leukemic Inv(16) fusion gene CBFB-MYH11 Current Topics in Microbiology and Immunology. 211: 289-298. PMID 8585960  1
1996 Rosenfeld MA, Collins FS. Gene therapy for cystic fibrosis Chest. 109: 241-252. PMID 8549191 DOI: 10.1378/Chest.109.1.241  1
1996 Collins FS. BRCA1 - Lots of mutations, lots of dilemmas New England Journal of Medicine. 334: 186-188. PMID 8531977 DOI: 10.1056/Nejm199601183340311  1
1995 Merajver SD, Frank TS, Xu J, Pham TM, Calzone KA, Bennett-Baker P, Chamberlain J, Boyd J, Garber JE, Collins FS. Germline BRCA1 mutations and loss of the wild-type allele in tumors from families with early onset breast and ovarian cancer. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 1: 539-44. PMID 9816013  1
1995 Ho PP, Couch FJ, Brody LC, Abel KJ, Boehnke M, Shearon TH, Chandrasekharappa SC, Collins FS. Localization of the human homolog of the yeast cell division control 27 gene (CDC27) proximal to ITGB3 on human chromosome 17q21.3 Somatic Cell and Molecular Genetics. 21: 351-355. PMID 8619132 DOI: 10.1007/BF02257470  1
1995 Smith JR, Carpten JD, Brownstein MJ, Ghosh S, Magnuson VL, Gilbert DA, Trent JM, Collins FS. Approach to genotyping errors caused by nontemplated nucleotide addition by Taq DNA polymerase. Genome Research. 5: 312-7. PMID 8593617 DOI: 10.1101/Gr.5.3.312  1
1995 Savitsky K, Sfez S, Tagle DA, Ziv Y, Sartiel A, Collins FS, Shiloh Y, Rotman G. The complete sequence of the coding region of the ATM gene reveals similarity to cell cycle regulators in different species. Human Molecular Genetics. 4: 2025-32. PMID 8589678 DOI: 10.1093/Hmg/4.11.2025  1
1995 Hajra A, Liu PP, Wang Q, Kelley CA, Stacy T, Adelstein RS, Speck NA, Collins FS. The leukemic core binding factor β-smooth muscle myosin heavy chain (CBFβ-SMMHC) chimeric protein requires both CBFβ and myosin heavy chain domains for transformation of NIH 3T3 cells Proceedings of the National Academy of Sciences of the United States of America. 92: 1926-1930. PMID 7892201 DOI: 10.1073/Pnas.92.6.1926  1
1995 Merajver SD, Pham TM, Caduff RF, Chen M, Poy EL, Cooney KA, Weber BL, Collins FS, Johnston C, Frank TS. Somatic mutations in the BRCA1 gene in sporadic ovarian tumours. Nature Genetics. 9: 439-43. PMID 7795652 DOI: 10.1038/Ng0495-439  1
1995 Collins FS. Positional cloning moves from perditional to traditional Nature Genetics. 9: 347-350. PMID 7795639 DOI: 10.1038/Ng0495-347  1
1995 Savitsky K, Bar-Shira A, Gilad S, Rotman G, Ziv Y, Vanagaite L, Tagle DA, Smith S, Uziel T, Sfez S, Ashkenazi M, Pecker I, Frydman M, Harnik R, Patanjali SR, ... ... Collins FS, et al. A single ataxia telangiectasia gene with a product similar to PI-3 kinase. Science (New York, N.Y.). 268: 1749-53. PMID 7792600  1
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, ... ... Collins FS, 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  1
1995 Brody LC, Abel KJ, Castilla LH, Couch FJ, McKinley DR, Yin G, Ho PP, Merajver S, Chandrasekharappa SC, Xu J, Cole JL, Struewing JP, Valdes JM, Collins FS, Weber BL. Construction of a transcription map surrounding the BRCA1 locus of human chromosome 17 Genomics. 25: 238-247. PMID 7774924 DOI: 10.1016/0888-7543(95)80131-5  1
1995 Smit LS, Strong TV, Wilkinson DJ, Macek M, Mansoura MK, Wood DL, Cole JL, Cutting GR, Cohn JA, Dawson DC. Missense mutation (G480C) in the CFTR gene associated with protein mislocalization but normal chloride channel activity. Human Molecular Genetics. 4: 269-73. PMID 7757078 DOI: 10.1093/Hmg/4.2.269  1
1995 Weber BL, Abel KJ, Couch FJ, Merajver S, Castilla L, Brody LC, Collins FS. Transcript identification in the BRCA1 candidate region Breast Cancer Research and Treatment. 33: 115-124. PMID 7749139 DOI: 10.1007/Bf00682719  1
1995 Liu PP, Hajra A, Wijmenga C, Collins FS. Molecular pathogenesis of the chromosome 16 inversion in the M4Eo subtype of acute myeloid leukemia Blood. 85: 2289-2302. PMID 7727763 DOI: 10.1182/Blood.V85.9.2289.Bloodjournal8592289  1
1995 Couch FJ, Kiousis S, Castilla LH, Xu J, Chandrasekharappa SC, Chamberlain JS, Collins FS, Weber BL. Characterization of 10 new polymorphic dinucleotide repeats and generation of a high-density microsatellite-based physical map of the BRCA1 region of chromosome 17q21. Genomics. 24: 419-24. PMID 7713491 DOI: 10.1006/Geno.1994.1647  0.32
1995 Vanagaite L, James MR, Rotman G, Savitsky K, Bar-Shira A, Gilad S, Ziv Y, Uchenik V, Sartiel A, Collins FS, Sheffield VC, Richard CW, Weissenbach J, Shiloh Y. A high-density microsatellite map of the ataxia-telangiectasia locus. Human Genetics. 95: 451-4. PMID 7705845 DOI: 10.1007/Bf00208975  1
1995 Hajra A, Liu PP, Speck NA, Collins FS. Overexpression of core-binding factor α (CBFα) reverses cellular transformation by the CBFβ-smooth muscle myosin heavy chain chimeric oncoprotein Molecular and Cellular Biology. 15: 4980-4989. PMID 7651416 DOI: 10.1128/Mcb.15.9.4980  1
1995 Rotman G, Vanagaite L, Collins FS, Shiloh Y. Rapid identification of polymorphic CA-repeats in YAC clones Molecular Biotechnology. 3: 85-92. PMID 7620980 DOI: 10.1007/Bf02789104  1
1995 Gutmann DH, Cole JL, Collins FS. Expression of the neurofibromatosis type 1 (NF1) gene during mouse embryonic development. Progress in Brain Research. 105: 327-35. PMID 7568895 DOI: 10.1016/S0079-6123(08)63311-7  1
1995 Struewing JP, Abeliovich D, Peretz T, Avishai N, Kaback MM, Collins FS, Brody LC. The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals Nature Genetics. 11: 198-200. PMID 7550349 DOI: 10.1038/Ng1095-198  1
1995 Morrow DM, Tagle DA, Shiloh Y, Collins FS, Hieter P. TEL1, an S. cerevisiae homolog of the human gene mutated in ataxia telangiectasia, is functionally related to the yeast checkpoint gene MEC1 Cell. 82: 831-840. PMID 7545545 DOI: 10.1016/0092-8674(95)90480-8  1
1995 Guyer MS, Collins FS. How is the Human Genome Project doing, and what have we learned so far? Proceedings of the National Academy of Sciences of the United States of America. 92: 10841-10848. PMID 7479895 DOI: 10.1073/Pnas.92.24.10841  1
1995 Collins FS. Ahead of schedule and under budget: The Genome Project passes its fifth birthday Proceedings of the National Academy of Sciences of the United States of America. 92: 10821-10823. PMID 7479891 DOI: 10.1073/Pnas.92.24.10821  1
1994 Boyer MJ, Gutmann DH, Collins FS, Bar-Sagi D. Crosslinking of the surface immunoglobulin receptor in B lymphocytes induces a redistribution of neurofibromin but not p120-GAP Oncogene. 9: 349-357. PMID 8290249  1
1994 Valdes JM, Tagle DA, Collins FS. Island rescue PCR: A rapid and efficient method for isolating transcribed sequences from yeast artificial chromosomes and cosmids Proceedings of the National Academy of Sciences of the United States of America. 91: 5377-5381. PMID 8202494 DOI: 10.1073/Pnas.91.12.5377  1
1994 Gutmann DH, Cole JL, Collins FS. Modulation of neurofibromatosis type 1 gene expression during in vitro myoblast differentiation. Journal of Neuroscience Research. 37: 398-405. PMID 8176761 DOI: 10.1002/Jnr.490370312  1
1994 McDonald MT, Papenberg KA, Ghosh S, Glatfelter AA, Biesecker BB, Helmbold EA, Markel DS, Zolotor A, McKinnon WC, Vanderstoep JL, Jackson CE, Iannuzzi M, Collins FS, Boehnke M, Porteous ME, et al. A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33-34 Nature Genetics. 6: 197-204. PMID 8162075 DOI: 10.1038/Ng0294-197  1
1994 Collins FS, Benjamin LJ, Botstein D, Cox JR, Davidson N, Gray JW, Housman DE, Holtzman N, Jamison KR, Rothstein R, Smith DC, Smith LM, Spence MA, Tilghman SM. Statement on Use of DNA Testing for Presymptomatic Identification of Cancer Risk Jama: the Journal of the American Medical Association. 271: 785. PMID 8114217 DOI: 10.1001/Jama.1994.03510340075038  1
1994 Couch FJ, Abel KJ, Brody LC, Boehnke M, Collins FS, Weber BL. Localization of the Gene for ATP Citrate Lyase (ACLY) Distal to Gastrin (GAS) and Proximal to D17S856 on Chromosome 17q12-q21 Genomics. 21: 444-446. PMID 8088842 DOI: 10.1006/Geno.1994.1293  1
1994 Legius E, Hall BK, Wallace MR, Collins FS, Glover TW. Ten base pair duplication in exon 38 of the NF1 gene. Human Molecular Genetics. 3: 829-30. PMID 8081372 DOI: 10.1093/Hmg/3.5.829  0.36
1994 Weber BL, Abel KJ, Brody LC, Flejter WL, Chandrasekharappa SC, Couch FJ, Merajver SD, Collins FS. Familial breast cancer: Approaching the isolation of a susceptibility gene Cancer. 74: 1013-1020. PMID 8039134 DOI: 10.1002/1097-0142(19940801)74:3+<1013::Aid-Cncr2820741507>3.0.Co;2-#  1
1994 Vanagaite L, Savitsky K, Rotman G, Ziv Y, Gerken SC, White R, Weissenbach J, Gillett G, Benham FJ, Richard CW, James MR, Collins FS, Shiloh Y. Physical localization of microsatellite markers at the ataxia-telangiectasia locus at 11q22-q23. Genomics. 22: 231-3. PMID 7959777 DOI: 10.1006/Geno.1994.1370  1
1994 Castilla LH, Couch FJ, Erdos MR, Hoskins KF, Calzone K, Garber JE, Boyd J, Lubin MB, Deshano ML, Brody LC, Collins FS, Weber BL. Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer Nature Genetics. 8: 387-391. PMID 7894491 DOI: 10.1038/Ng1294-387  1
1994 Rotman G, Vanagaite L, Collins FS, Shiloh Y. Three dinucleotide repeat polymorphisms at the ataxia-telangiectasia locus Human Molecular Genetics. 3: 2079. PMID 7874134  1
1994 Gottesman MM, Collins FS. The Role of the Human Genome Project in Disease Prevention Preventive Medicine. 23: 591-594. PMID 7845920 DOI: 10.1006/pmed.1994.1094  1
1994 Rotman G, Savitsky K, Ziv Y, Cole CG, Higgins MJ, Bar-Am I, Dunham I, Bar-Shira A, Vanagaite L, Qin S, Zhang J, Nowak NJ, Chandrasekharappa SC, Lehrach H, Avivi L, ... ... Collins FS, et al. A YAC contig spanning the ataxia-telangiectasia locus (groups A and C) at 11q22-q23. Genomics. 24: 234-42. PMID 7698744 DOI: 10.1006/Geno.1994.1611  1
1994 Liu P, Seidel N, Bodine D, Speck N, Tarlé S, Collins FS. Acute myeloid leukemia with Inv (16) produces a chimeric transcription factor with a myosin heavy chain tail. Cold Spring Harbor Symposia On Quantitative Biology. 59: 547-53. PMID 7587111 DOI: 10.1101/Sqb.1994.059.01.061  1
1994 Nasr SZ, Strong TV, Collins FS. Identification of a CFTR frameshift mutation (1013 delAA) in trans to delta F508 in a pancreatic sufficient cystic fibrosis patient. Human Molecular Genetics. 3: 2063-4. PMID 7533026  1
1994 Gutmann DH, Cole JL, Stone WJ, Ponder BA, Collins FS. Loss of neurofibromin in adrenal gland tumors from patients with neurofibromatosis type I. Genes, Chromosomes & Cancer. 10: 55-8. PMID 7519874 DOI: 10.1002/Gcc.2870100109  1
1994 Strong TV, Boehm K, Collins FS. Localization of cystic fibrosis transmembrane conductance regulator mRNA in the human gastrointestinal tract by in situ hybridization Journal of Clinical Investigation. 93: 347-354. PMID 7506713 DOI: 10.1172/Jci116966  1
1994 Collins FS. Response [2] Science. 264: 13-14. DOI: 10.1126/Science.334.6058.903  1
1993 Legius E, Marchuk DA, Collins FS, Glover TW. Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis. Nature Genetics. 3: 122-6. PMID 8499945 DOI: 10.1038/Ng0293-122  1
1993 Andersen LB, Fountain JW, Gutmann DH, Tarlé SA, Glover TW, Dracopoli NC, Housman DE, Collins FS. Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell lines. Nature Genetics. 3: 118-21. PMID 8499944 DOI: 10.1038/Ng0293-118  0.36
1993 Gutmann DH, Collins FS. The neurofibromatosis type 1 gene and its protein product, neurofibromin Neuron. 10: 335-343. PMID 8461130 DOI: 10.1016/0896-6273(93)90324-K  1
1993 MacDonald ME, Ambrose CM, Duyao MP, Myers RH, Lin C, Srinidhi L, Barnes G, Taylor SA, James M, Groot N, MacFarlane H, Jenkins B, Anderson MA, Wexler NS, Gusella JF, ... ... Collins FS, et al. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes Cell. 72: 971-983. PMID 8458085 DOI: 10.1016/0092-8674(93)90585-E  1
1993 Tagle DA, Swaroop M, Lovett M, Collins FS. Magnetic bead capture of expressed sequences encoded within large genomic segments. Nature. 361: 751-3. PMID 8441473 DOI: 10.1038/361751A0  1
1993 Gutmann DH, Boguski M, Marchuk D, Wigler M, Collins FS, Ballester R. Analysis of the neurofibromatosis type 1 (NF1) GAP-related domain by site-directed mutagenesis. Oncogene. 8: 761-9. PMID 8437860  1
1993 Andersen LB, Ballester R, Marchuk DA, Chang E, Gutmann DH, Saulino AM, Camonis J, Wigler M, Collins FS. A conserved alternative splice in the von Recklinghausen neurofibromatosis (NF1) gene produces two neurofibromin isoforms, both of which have GTPase-activating protein activity. Molecular and Cellular Biology. 13: 487-95. PMID 8417346 DOI: 10.1128/Mcb.13.1.487  1
1993 Decker RA, Collins FS. Dinucleotide repeat polymorphism at the D10S469 locus Human Molecular Genetics. 2: 1330. PMID 8401525 DOI: 10.1093/Hmg/2.8.1330-A  1
1993 Gutman DH, Andersen LB, Cole JL, Swaroop M, Collins FS. An alternatively-spliced mRNA in the carboxy terminus of the neurofibromatosis type 1 (NF1) gene is expressed in muscle. Human Molecular Genetics. 2: 989-92. PMID 8364582 DOI: 10.1093/Hmg/2.7.989  1
1993 Andersen LB, Tarlé SA, Marchuk DA, Legius E, Collins FS. A compound nucleotide repeat in the neurofibromatosis (NF1) gene. Human Molecular Genetics. 2: 1083. PMID 8364559 DOI: 10.1093/Hmg/2.7.1083-A  0.36
1993 Valdes JM, Tagle DA, Elmer LW, Collins FS. A simple non-radioactive method for diagnosis of huntington's disease Human Molecular Genetics. 2: 633-634. PMID 8353481 DOI: 10.1093/Hmg/2.6.633  1
1993 Baxendale S, MacDonald ME, Mott R, Francis F, Lin C, Kirby SF, James M, Zehetner G, Hummerich H, Valdes J. A cosmid contig and high resolution restriction map of the 2 megabase region containing the Huntington's disease gene. Nature Genetics. 4: 181-6. PMID 8348156 DOI: 10.1038/Ng0693-181  1
1993 Gregory PE, Gutmann DH, Mitchell A, Park S, Boguski M, Jacks T, Wood DL, Jove R, Collins FS. Neurofibromatosis type 1 gene product (neurofibromin) associates with microtubules. Somatic Cell and Molecular Genetics. 19: 265-74. PMID 8332934 DOI: 10.1007/Bf01233074  0.36
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  1
1993 Strong TV, Tagle DA, Valdes JM, Elmer LW, Boehm K, Swaroop M, Kaatz KW, Collins FS, Albin RL. Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues. Nature Genetics. 5: 259-65. PMID 8275091 DOI: 10.1038/Ng1193-259  1
1993 Colman SD, Collins FS, Wallace MR. Characterization of a single base-pair deletion in neurofibromatosis type 1 Human Molecular Genetics. 2: 1709-1711. PMID 8268926 DOI: 10.1093/Hmg/2.10.1709  1
1993 Flejter WL, Barcroft CL, Guo SW, Lynch ED, Boehnke M, Chandrasekharappa S, Hayes S, Collins FS, Weber BL, Glover TW. Multicolor FISH Mapping with Alu-PCR-Amplified YAC Clone DNA Determines the Order of Markers in the BRCA1 Region on Chromosome 17q12-q21 Genomics. 17: 624-631. PMID 8244379 DOI: 10.1006/geno.1993.1382  1
1993 Gutmann DH, Collins FS. Neurofibromatosis Type 1: Beyond Positional Cloning Archives of Neurology. 50: 1185-1193. PMID 8215978 DOI: 10.1001/Archneur.1993.00540110065007  1
1993 Reyniers E, De Boulle K, Marchuk DA, Andersen LB, Collins FS, Willems PJ. An EcoRI RFLP in the 5' region of the human NF1 gene. Human Genetics. 92: 631. PMID 7903272 DOI: 10.1007/Bf00420953  0.36
1993 Drumm ML, Collins FS. Molecular biology of cystic fibrosis Molecular Genetic Medicine. 3: 33-68. PMID 7693108 DOI: 10.1016/B978-0-12-462003-2.50006-7  1
1993 Yang Y, Devor DC, Engelhardt JF, Ernst SA, Strong TV, Collins FS, Cohn JA, Frizzell RA, Wilson JM. Molecular basis of defective anion transport in L cells expressing recombinant forms of CFTR. Human Molecular Genetics. 2: 1253-61. PMID 7691345 DOI: 10.1093/Hmg/2.8.1253  1
1993 Koh J, Sferra TJ, Collins FS. Characterization of the cystic fibrosis transmembrane conductance regulator promoter region: Chromatin context and tissue-specificity Journal of Biological Chemistry. 268: 15912-15921. PMID 7688000  1
1993 Smit LS, Nasr SZ, Iannuzzi MC, Collins FS. An African-American cystic fibrosis patient homozygous for a novel frameshift mutation associated with reduced CFTR mRNA levels. Human Mutation. 2: 148-51. PMID 7686423 DOI: 10.1002/Humu.1380020217  1
1993 Chandrasekharappa SC, Gross LA, King SE, Collins FS. The human NME2 gene lies within 18kb of NME1 in chromosome 17 Genes Chromosomes and Cancer. 6: 245-248. PMID 7685630 DOI: 10.1002/Gcc.2870060411  1
1993 Strong TV, Wilkinson DJ, Monsoura MK, Devor DC, Henze K, Yang Y, Wilson JM, Cohn JA, Dawson DC, Frizzell RA, Collins FS. Expression of an abundant alternatively spliced form of the cystic fibrosis transmembrane conductance regulator (CFTR) gene is not associated with a camp-activated chloride conductance Human Molecular Genetics. 2: 225-230. PMID 7684641 DOI: 10.1093/Hmg/2.3.225  1
1993 Sferra TJ, Collins FS. The molecular biology of cystic fibrosis Annual Review of Medicine. 44: 133-144. PMID 7682803 DOI: 10.1146/Annurev.Me.44.020193.001025  1
1993 Gutmann DH, Tennekoon GI, Cole JL, Collins FS, Rutkowski JL. Modulation of the neurofibromatosis type 1 gene product, neurofibromin, during Schwann cell differentiation. Journal of Neuroscience Research. 36: 216-23. PMID 7505343 DOI: 10.1002/Jnr.490360212  1
1993 Cohn JA, Strong TV, Picciotto MR, Nairn AC, Collins FS, Fitz JG. Localization of the cystic fibrosis transmembrane conductance regulator in human bile duct epithelial cells. Gastroenterology. 105: 1857-64. PMID 7504645 DOI: 10.1016/0016-5085(93)91085-V  1
1992 Chandrasekharappa SC, Marchuk DA, Collins FS. Analysis of yeast artificial chromosome clones. Methods in Molecular Biology (Clifton, N.J.). 12: 235-57. PMID 21409638 DOI: 10.1385/0-89603-229-9:235  0.36
1992 Marchuk DA, Tavakkol R, Wallace MR, Brownstein BH, Taillon-Miller P, Fong CT, Legius E, Andersen LB, Glover TW, Collins FS. A yeast artificial chromosome contig encompassing the type 1 neurofibromatosis gene. Genomics. 13: 672-80. PMID 1639394 DOI: 10.1016/0888-7543(92)90140-N  0.36
1992 Gutmann DH, Collins FS. Recent progress toward understanding the molecular biology of von Recklinghausen neurofibromatosis Annals of Neurology. 31: 555-561. PMID 1596091 DOI: 10.1002/Ana.410310515  1
1992 Wilson JM, Collins FS. More from the modellers Nature. 359: 195-196. PMID 1528259 DOI: 10.1038/359195A0  1
1992 Collins FS, Wilson JM. A welcome animal model Nature. 358: 708-709. PMID 1508266 DOI: 10.1038/358708A0  1
1992 Legius E, Marchuk DA, Hall BK, Andersen LB, Wallace MR, Collins FS, Glover TW. NF1-related locus on chromosome 15. Genomics. 13: 1316-8. PMID 1505963 DOI: 10.1016/0888-7543(92)90055-W  0.36
1992 Gumucio DL, Heilstedt-Williamson H, Gray TA, Tarlé SA, Shelton DA, Tagle DA, Slightom JL, Goodman M, Collins FS. Phylogenetic footprinting reveals a nuclear protein which binds to silencer sequences in the human γ and ε globin genes Molecular and Cellular Biology. 12: 4919-4929. PMID 1406669 DOI: 10.1128/Mcb.12.11.4919  1
1992 Collins FS. Cystic fibrosis: Molecular biology and therapeutic implications Science. 256: 774-779. PMID 1375392 DOI: 10.1126/Science.1375392  1
1992 Kayes LM, Schroeder WT, Marchuk DA, Collins FS, Riccardi VM, Duvic M, Stephens K. The gene for a novel epidermal antigen maps near the neurofibromatosis 1 gene. Genomics. 14: 369-76. PMID 1358802 DOI: 10.1016/S0888-7543(05)80228-9  0.36
1992 McCombie WR, Martin-Gallardo A, Gocayne JD, FitzGerald M, Dubnick M, Kelley JM, Castilla L, Liu LI, Wallace S, Trapp S, Tagle D, Whaley WL, Cheng S, Gusella J, Frischauf AM, ... ... Collins FS, et al. Expressed genes, Alu repeats and polymorphisms in cosmids sequenced from chromosome 4p16.3 Nature Genetics. 1: 348-353. PMID 1338771 DOI: 10.1038/Ng0892-348  1
1992 Martin-Gallardo A, Marchuk DA, Gocayne J, Kerlavage AR, McCombie WR, Venter JC, Collins FS, Wallace MR. Sequencing and analysis of genomic fragments from the NF1 locus. Dna Sequence : the Journal of Dna Sequencing and Mapping. 3: 237-43. PMID 1338369 DOI: 10.3109/10425179209034023  0.36
1992 Bates GP, Valdes J, Hummerich H, Baxendale S, Le Paslier DL, Monaco AP, Tagle D, MacDonald ME, Altherr M, Ross M. Characterization of a yeast artificial chromosome contig spanning the Huntington's disease gene candidate region. Nature Genetics. 1: 180-7. PMID 1303232 DOI: 10.1038/Ng0692-180  1
1992 Tagle DA, Blanchard-mcquate KL, Collins FS. Dinucleotide repeat polymorphism in the huntington's disease region at the D4S43 locus Human Molecular Genetics. 1: 215. PMID 1303186 DOI: 10.1093/hmg/1.3.215  1
1992 Collins FS. Positional cloning: Let’s not call it reverse anymore Nature Genetics. 1: 3-6. PMID 1301996 DOI: 10.1038/Ng0492-3  1
1992 Tagle DA, Collins FS. An optimized Alu-PCR primer pair for human-specific amplification of YACS and somatic cell hybrids Human Molecular Genetics. 1: 121-122. PMID 1301148 DOI: 10.1093/Hmg/1.2.121  1
1992 Strong TV, Smit LS, Nasr S, Wood DL, Cole JL, Iannuzzi MC, Stern RC, Collins FS. Characterization of an intron 12 splice donor mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Human Mutation. 1: 380-7. PMID 1284540 DOI: 10.1002/Humu.1380010506  1
1991 Marchuk D, Drumm M, Saulino A, Collins FS. Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR products. Nucleic Acids Research. 19: 1154. PMID 2020552 DOI: 10.1093/Nar/19.5.1154  1
1991 Collins FS. The Genome Project and human health Faseb Journal. 5: 77. PMID 1991592 DOI: 10.1096/Fasebj.5.1.1991592  1
1991 Goldberg NS, Collins FS. The Hunt for the Neurofibromatosis Gene Archives of Dermatology. 127: 1705-1707. PMID 1952978 DOI: 10.1001/archderm.1991.01680100105014  1
1991 Gutmann DH, Wood DL, Collins FS. Identification of the neurofibromatosis type 1 gene product Proceedings of the National Academy of Sciences of the United States of America. 88: 9658-9662. PMID 1946382 DOI: 10.1073/Pnas.88.21.9658  1
1991 Strong TV, Smit LS, Turpin SV, Cole JL, Hon CT, Markiewicz D, Petty TL, Craig MW, Rosenow EC, Tsui LC. Cystic fibrosis gene mutation in two sisters with mild disease and normal sweat electrolyte levels. The New England Journal of Medicine. 325: 1630-4. PMID 1944451 DOI: 10.1056/Nejm199112053252307  1
1991 Collins FS. Identification of disease genes: Recent successes Hospital Practice. 26: 93-98. PMID 1918209 DOI: 10.1080/21548331.1991.11705307  1
1991 Shukla H, Gillespie GA, Srivastava R, Collins FS, Chorney MJ. A class I jumping clone places the HLA-G gene approximately 100 kilobases from HLA-H within the HLA-A subregion of the human MHC. Genomics. 10: 905-914. PMID 1916822 DOI: 10.1016/0888-7543(91)90178-H  0.4
1991 Gumucio DL, Rood KL, Blanchard-McQuate KL, Gray TA, Saulino A, Collins FS. Interaction of Sp1 with the human gamma globin promoter: binding and transactivation of normal and mutant promoters. Blood. 78: 1853-63. PMID 1912570 DOI: 10.1182/Blood.V78.7.1853.Bloodjournal7871853  1
1991 Collins FS. Medical and ethical consequences of the human genome project The Journal of Clinical Ethics. 2: 260-267. PMID 1804396  1
1991 Wallace MR, Collins FS. Molecular genetics of von Recklinghausen neurofibromatosis Advances in Human Genetics. 20: 267-307. PMID 1801591 DOI: 10.1007/978-1-4684-5958-6_5  1
1991 Marchuk DA, Saulino AM, Tavakkol R, Swaroop M, Wallace MR, Andersen LB, Mitchell AL, Gutmann DH, Boguski M, Collins FS. cDNA cloning of the type 1 neurofibromatosis gene: complete sequence of the NF1 gene product. Genomics. 11: 931-40. PMID 1783401 DOI: 10.1016/0888-7543(91)90017-9  1
1991 Collins FS. Of needles and haystacks: finding human disease genes by positional cloning Clinical Research. 39: 615-623. PMID 1764889  1
1991 Gibson AL, Wagner LM, Collins FS, Oxender DL. A bacterial system for investigating transport effects of cystic fibrosis--associated mutations. Science (New York, N.Y.). 254: 109-11. PMID 1718037 DOI: 10.1126/Science.1718037  1
1991 Ton CCT, Hirvonen H, Miwa H, Weil MM, Monaghan P, Jordan T, van Heyningen V, Hastie ND, Meijers-Heijboer H, Drechsler M, Royer-Pokora B, Collins F, Swaroop A, Strong LC, Saunders GF. Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region Cell. 67: 1059-1074. PMID 1684738 DOI: 10.1016/0092-8674(91)90284-6  1
1991 Andersen LB, Wallace MR, Marchuk DA, Tavakkol R, Mitchell A, Saulino AM, Collins FS. A highly polymorphic cDNA probe in the NF1 gene. Nucleic Acids Research. 19: 3754. PMID 1677185 DOI: 10.1093/Nar/19.13.3754  0.36
1991 Andersen LB, Wallace MR, Marchuk DA, Cawthon RM, Odeh HM, Letcher R, White RL, Collins FS. A polymorphic cDNA probe on chromosome 17q11.2 located within the NF1 gene [D17S376]. Nucleic Acids Research. 19: 197. PMID 1672744 DOI: 10.1093/nar/19.1.197-a  1
1991 Allitto BA, MacDonald ME, Bucan M, Richards J, Romano D, Whaley WL, Falcone B, Ianazzi J, Wexler NS, Wasmuth JJ. Increased recombination adjacent to the Huntington disease-linked D4S10 marker. Genomics. 9: 104-12. PMID 1672283 DOI: 10.1016/0888-7543(91)90226-5  1
1990 Ledbetter SA, Wallace MR, Collins FS, Ledbetter DH. Human chromosome 17 NotI linking clones and their use in long-range restriction mapping of the Miller-Dieker chromosome region (MDCR) in 17p13.3 Genomics. 7: 264-269. PMID 2347590 DOI: 10.1016/0888-7543(90)90549-A  1
1990 Merry DE, Lesko JG, Siu V, Funtoff WF, Collins F, Lewis RA, Nussbaum RL. DXS165 detects a translocation breakpoint in a woman with choroideremia and a de novo X; 13 translocation Genomics. 6: 609-615. PMID 2341150 DOI: 10.1016/0888-7543(90)90494-F  1
1990 Tanaka M, Nolan JA, Bhargava AK, Rood K, Collins FS, Weissman SM, Forget BG, Chamberlain JW. Expression of human globin genes in transgenic mice carrying the beta-globin gene cluster with a mutation causing G gamma beta + hereditary persistence of fetal hemoglobin. Annals of the New York Academy of Sciences. 612: 167-78. PMID 2291546 DOI: 10.1111/J.1749-6632.1990.Tb24303.X  1
1990 Wallace MR, Andersen LB, Fountain JW, Odeh HM, Viskochil D, Marchuk DA, O'Connell P, White R, Collins FS. A chromosome jump crosses a translocation breakpoint in the von Recklinghausen neurofibromatosis region. Genes, Chromosomes & Cancer. 2: 271-7. PMID 2176541 DOI: 10.1002/Gcc.2870020404  1
1990 Collins FS. Identifying human disease genes by positional cloning Harvey Lectures. 86: 149-164. PMID 2152136  1
1990 Lux SE, Tse WT, Menninger JC, John KM, Harris P, Shalev O, Chilcote RR, Marchesi SL, Watkins PC, Bennett V, McIntosh S, Collins FS, Francke U, Ward DC, Forget BG. Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8 Nature. 345: 736-739. PMID 2141669 DOI: 10.1038/345736A0  1
1990 Bu?an M, Zimmer M, Whaley WL, Poustka A, Youngman S, Allitto BA, Ormondroyd E, Smith B, Pohl TM, MacDonald M, Bates GP, Richards J, Volinia S, Gilliam TC, Sedlacek Z, ... Collins FS, et al. Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation Genomics. 6: 1-15. PMID 2137426 DOI: 10.1016/0888-7543(90)90442-W  1
1990 Wallace MR, Marchuk DA, Andersen LB, Letcher R, Odeh HM, Saulino AM, Fountain JW, Brereton A, Nicholson J, Mitchell AL, Brownstein BH, Collins FS. Type 1 neurofibromatosis gene: Identification of a large transcript disrupted in three NF1 patients Science. 249: 181-186. PMID 2134734 DOI: 10.1126/Science.2134734  1
1990 Ballester R, Marchuk D, Boguski M, Saulino A, Letcher R, Wigler M, Collins F. The NF1 locus encodes a protein functionally related to mammalian GAP and yeast IRA proteins. Cell. 63: 851-9. PMID 2121371 DOI: 10.1016/0092-8674(90)90151-4  1
1990 Dean M, Amos JA, Lynch J, Romeo G, Devoto M, Ward K, Halley D, Oostra B, Ferrari M, Russo S. Prenatal diagnosis and linkage disequilibrium with cystic fibrosis for markers surrounding D7S8. Human Genetics. 85: 275-8. PMID 1975555 DOI: 10.1007/Bf00206745  1
1990 Walker AP, Collins FS, Siddique T, Yamaoka LH, Herbstreith MH, Pericak-Vance MA, Secore SL, Hung WY, Goate AM, Hardy JA. D21S194, a jump clone from D21S16. Nucleic Acids Research. 18: 1931. PMID 1970875 DOI: 10.1093/Nar/18.7.1931-A  1
1990 Dean M, Drumm ML, Stewart C, Gerrard B, Perry A, Hidaka N, Cole JL, Collins FS, Iannuzzi MC. Approaches to localizing disease genes as applied to cystic fibrosis. Nucleic Acids Research. 18: 345-50. PMID 1970161 DOI: 10.1093/Nar/18.2.345  1
1990 Patel PI, Ledbetter DH, Frances S, Franco B, Wallace MR, Collins FS, Lupski JR. Isolation of a polymorphic DNA sequence (LL101) from the short arm of chromosome 17 [D17S251] Nucleic Acids Research. 18: 1087-1087. PMID 1969146 DOI: 10.1093/Nar/18.4.1087  0.36
1990 Collins FS, Riordan JR, Tsui LC. The cystic fibrosis gene: Isolation and significance Hospital Practice. 25: 47-57. PMID 1698801 DOI: 10.1080/21548331.1990.11704019  1
1990 Donlon TA, Krensky AM, Wallace MR, Collins FS, Lovett M, Clayberger C. Localization of a human T-cell-specific gene, RANTES (D17S136E), to chromosome 17q11.2-q12. Genomics. 6: 548-53. PMID 1691736 DOI: 10.1016/0888-7543(90)90485-D  0.36
1990 Iannuzzi MC, Collins FS. Reverse genetics and cystic fibrosis American Journal of Respiratory Cell and Molecular Biology. 2: 309-316. PMID 1691007 DOI: 10.1165/Ajrcmb/2.4.309  1
1990 Gumucio DL, Lockwood WK, Weber JL, Saulino AM, Delgrosso K, Surrey S, Schwartz E, Goodman M, Collins FS. The -175T → C mutation increases promoter strength in erythroid cells: Correlation with evolutionary conservation of binding sites for two trans-acting factors Blood. 75: 756-761. PMID 1688723 DOI: 10.1182/Blood.V75.3.756.Bloodjournal753756  1
1989 Wallace MR, Fountain JW, Brereton AM, Collins FS. Direct construction of a chromosome-specific Noti linking library from flow-sorted chromosomes Nucleic Acids Research. 17: 1665-1677. PMID 2784207 DOI: 10.1093/Nar/17.4.1665  1
1989 Rommens JM, Iannuzzi MC, Kerem B, Drumm ML, Melmer G, Dean M, Rozmahel R, Cole JL, Kennedy D, Hidaka N. Identification of the cystic fibrosis gene: chromosome walking and jumping. Science (New York, N.Y.). 245: 1059-65. PMID 2772657 DOI: 10.1126/Science.2772657  1
1989 Dean M, Stewart C, Perry A, Gerrard B, Beck T, Rapp U, Drumm M, Iannuzzi M, Collins F, O'Brien S. Genetic markers for oncogenes, growth factors, and cystic fibrosis Hamatologie Und Bluttransfusion. 32: 360-365. PMID 2576235 DOI: 10.1007/978-3-642-74621-5_63  1
1989 Boehnke M, Arnheim N, Li H, Collins FS. Fine-structure genetic mapping of human chromosomes using the polymerase chain reaction on single sperm: Experimental design considerations American Journal of Human Genetics. 45: 21-32. PMID 2568090  1
1989 Fountain JW, Wallace MR, Bruce MA, Seizinger BR, Menon AG, Gusella JF, Michels VV, Schmidt MA, Dewald GW, Collins FS. Physical mapping of a translocation breakpoint in neurofibromatosis Science. 244: 1085-1087. PMID 2543076 DOI: 10.1126/Science.2543076  1
1989 Nigro JM, Baker SJ, Preisinger AC, Jessup JM, Hostetter R, Cleary K, Bigner SH, Davidson N, Baylin S, Devilee P. Mutations in the p53 gene occur in diverse human tumour types. Nature. 342: 705-8. PMID 2531845 DOI: 10.1038/342705A0  1
1989 Collins FS, O'Connell P, Ponder BAJ, Seizinger BR. Progress towards identifying the neurofibromatosis (NF1) gene Trends in Genetics. 5: 217-221. PMID 2506682 DOI: 10.1016/0168-9525(89)90085-1  1
1988 Kenwrick SJ, Smith TJ, England S, Collins F, Davies KE. Localisation of the endpoints of deletions in the 5′ region of the duchenne gene using a sequence isolated by chromosome jumping Nucleic Acids Research. 16: 1305-1317. PMID 3347492 DOI: 10.1093/Nar/16.4.1305  1
1988 Engelke DR, Hoener PA, Collins FS. Direct sequencing of enzymatically amplified human genomic DNA Proceedings of the National Academy of Sciences of the United States of America. 85: 544-548. PMID 3267215 DOI: 10.1073/Pnas.85.2.544  1
1988 Marchuk D, Collins FS. pYAC-RC, a yeast artificial chromosome vector for cloning DNA cut with infrequently cutting restriction endonucleases. Nucleic Acids Research. 16: 7743. PMID 3045765 DOI: 10.1093/Nar/16.15.7743  1
1988 Richards JE, Gilliam TC, Cole JL, Drumm ML, Wasmuth JJ, Gusella JF, Collins FS. Chromosome jumping from D4S10 (G8) toward the Huntington disease gene. Proceedings of the National Academy of Sciences of the United States of America. 85: 6437-41. PMID 2901098 DOI: 10.1073/Pnas.85.17.6437  1
1988 Drumm ML, Smith CL, Dean M, Cole JL, Iannuzzi MC, Collins FS. Physical mapping of the cystic fibrosis region by pulsed-field gel electrophoresis. Genomics. 2: 346-54. PMID 2851537 DOI: 10.1016/0888-7543(88)90024-9  1
1988 Fountain JW, Lockwood WK, Collins FS. Transfection of primary human skin fibroblasts by electroporation Gene. 68: 167-172. PMID 2851491 DOI: 10.1016/0378-1119(88)90610-5  1
1988 Roth MS, Collins FS, Ginsburg D. Sizing of the human T cell receptor α locus and detection of a large deletion in the Molt-4 cell line Blood. 71: 1744-1747. PMID 2836005  1
1988 Gumucio DL, Rood KL, Gray TA, Riordan MF, Sartor CI, Collins FS. Nuclear proteins that bind the human gamma-globin gene promoter: alterations in binding produced by point mutations associated with hereditary persistence of fetal hemoglobin. Molecular and Cellular Biology. 8: 5310-22. PMID 2468996 DOI: 10.1128/Mcb.8.12.5310  1
1987 Treisman J, Collins FS. Adult Turner syndrome associated with chylous ascites and vascular anomalies. Clinical Genetics. 31: 218-23. PMID 3594929 DOI: 10.1111/J.1399-0004.1987.Tb02799.X  1
1987 Shows TB, McAlpine PJ, Boucheix C, Collins FS, Conneally PM, Frézal J, Gershowitz H, Goodfellow PN, Hall JG, Issitt P, Jones CA, Knowles BB, Lewis M, McKusick VA, Meisler M, et al. Guidelines for human gene nomenclature. An international system for human gene nomenclature (ISGN, 1987). Cytogenetics and Cell Genetics. 46: 11-28. PMID 3507270  1
1987 Collins FS, Drumm ML, Cole JL, Lockwood WK, Vande Woude GF, Iannuzzi MC. Construction of a general human chromosome jumping library, with application to cystic fibrosis. Science (New York, N.Y.). 235: 1046-9. PMID 2950591 DOI: 10.1126/Science.2950591  1
1987 Diehl SR, Boehnke M, Erickson RP, Baxter AB, Bruce MA, Lieberman JL, Platt DJ, Ploughman LM, Seiler KA, Sweet AM. Linkage analysis of von Recklinghausen neurofibromatosis to DNA markers on chromosome 17. Genomics. 1: 361-3. PMID 2896631 DOI: 10.1016/0888-7543(87)90039-5  1
1987 Iannuzzi MC, Konkle BA, Ginsburg D, Collins FS. Rsai RFLP in the human von willebrand factor gene Nucleic Acids Research. 15: 5909. PMID 2886983 DOI: 10.1093/Nar/15.16.6766  1
1987 Seizinger BR, Rouleau GA, Ozelius LJ, Lane AH, Faryniarz AG, Chao MV, Huson S, Korf BR, Parry DM, Pericak-Vance MA. Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene. Cell. 49: 589-94. PMID 2884037 DOI: 10.1016/0092-8674(87)90534-4  1
1987 Smith CL, Lawrance SK, Gillespie GA, Cantor CR, Weissman SM, Collins FS. Strategies for mapping and cloning macroregions of mammalian genomes Methods in Enzymology. 151: 461-489. PMID 2828836 DOI: 10.1016/S0076-6879(87)51038-2  1
1987 Collins FS, Cole JL, Lockwood WK, Iannuzzi MC. The deletion in both common types of hereditary persistence of fetal hemoglobin is approximately 105 kilobases. Blood. 70: 1797-803. PMID 2445400 DOI: 10.1182/Blood.V70.6.1797.Bloodjournal7061797  1
1986 Metherall JE, Collins FS, Pan J, Weissman SM, Forget BG. Beta zero thalassemia caused by a base substitution that creates an alternative splice acceptor site in an intron Embo Journal. 5: 2551-2557. PMID 3780671 DOI: 10.1002/J.1460-2075.1986.Tb04534.X  1
1986 Lawrence SK, Srivastava R, Rigas B, Chorney MJ, Gillespie GA, Smith CL, Cantor CR, Collins FS, Weissman SM. Molecular approaches to the characterization of megabase regions of DNA: Applications to the human major histocompatibility complex Cold Spring Harbor Symposia On Quantitative Biology. 51: 123-130. PMID 3472708 DOI: 10.1101/Sqb.1986.051.01.015  1
1985 Collins FS, Metherall JE, Yamakawa M, Pan J, Weissman SM, Forget BG. A point mutation in the Aγ-globin gene promoter in Greek hereditary persistence of fetal haemoglobin Nature. 313: 325-326. PMID 2578620 DOI: 10.1038/313325A0  1
1985 Feingold EA, Collins FS, Metherall JE, Stoeckert CJ, Weissman SM, Forget BG. Analysis of mutations associated with deletion and nondeletion hereditary persistence of fetal hemoglobin Progress in Clinical and Biological Research. 191: 107-124. PMID 2413468  1
1985 Feingold EA, Collins FS, Metherall JE, Stoeckert CJ, Weissman SM, Forget BG. Molecular analysis of deletion and nondeletion hereditary persistence of fetal hemoglobin and identification of a new mutation causing beta-thalassemia. Annals of the New York Academy of Sciences. 445: 159-69. PMID 2409868 DOI: 10.1111/J.1749-6632.1985.Tb17185.X  1
1984 Collins FS, Weissman SM. The molecular genetics of human hemoglobin Progress in Nucleic Acid Research and Molecular Biology. 31: 315-462. PMID 6397774  1
1984 Stoeckert CJ, Collins FS, Weissman SM. Human fetal globin DNA sequences suggest novel conversion event Nucleic Acids Research. 12: 4469-4479. PMID 6330670 DOI: 10.1093/nar/12.11.4469  1
1984 Collins FS, Boehm CD, Waber PG, Stoeckert CJ, Weissman SM, Forget BG, Kazazian HH. Concordance of a point mutation 5' to the (G)γ globin gene with (G)γβ+ hereditary persistence of fetal hemoglobin in the black population Blood. 64: 1292-1296. PMID 6208955  1
1984 Collins FS, Stoeckert CJ, Serjeant GR, Forget BG, Weissman SM. (G)γβ+ Hereditary persistence of fetal hemoglobin: Cosmid cloning and identification of a specific mutation 5' to the (G)γ gene Proceedings of the National Academy of Sciences of the United States of America. 81: 4894-4898. PMID 6205403 DOI: 10.1073/Pnas.81.15.4894  1
1984 Collins FS, Weissman SM. Directional cloning of DNA fragments at a large distance from an initial probe: A circularization method Proceedings of the National Academy of Sciences of the United States of America. 81: 6812-6816. PMID 6093122 DOI: 10.1073/Pnas.81.21.6812  1
1976 Collins FS, Cross RJ. Vibrationally inelastic scattering at high energies: H+ +H 2 The Journal of Chemical Physics. 65: 644-652.  1
1974 Collins FS, Preston RK, Cross RJ. Vibrationally inelastic scattering of H+ + H2 Chemical Physics Letters. 25: 608-610. DOI: 10.1016/0009-2614(74)85381-9  1
1972 Collins FS, George JK, Trindle C. Molecular orbital view of the stereochemical behavior in the interaction of bicyclo[2.1.0]pentane and unsaturated molecules Journal of the American Chemical Society. 94: 3732-3737.  1
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