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Francis Sellers Collins - Publications

Affiliations: 
National Human Genome Research Institute, USA 
Area:
Human Genetics
Website:
https://www.genome.gov/10000779/

284 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  0.96
2016 Lauer M, Valantine H, Collins FS. Policy: NIH push to stop sexual harassment. Nature. 531: 35. PMID 26935689 DOI: 10.1038/531035b  0.96
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  0.96
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  0.96
2015 Fauci AS, Collins FS. NIH research: think globally. Science (New York, N.Y.). 348: 159. PMID 25859018 DOI: 10.1126/science.aab2733  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2014 Collins FS, Tabak LA. Policy: NIH plans to enhance reproducibility. Nature. 505: 612-3. PMID 24482835 DOI: 10.1038/505612a  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2013 Hudson KL, Collins FS. Biospecimen policy: Family matters. Nature. 500: 141-2. PMID 23925224 DOI: 10.1038/500141a  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2012 Collins FS. NIH basics. Science (New York, N.Y.). 337: 503. PMID 22859455 DOI: 10.1126/science.1227820  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2011 Collins FS. Reengineering translational science: the time is right. Science Translational Medicine. 3: 90cm17. PMID 21734173 DOI: 10.1126/scitranslmed.3002747  0.96
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  0.96
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  0.96
2011 Collins FS. Mining for therapeutic gold. Nature Reviews. Drug Discovery. 10: 397. PMID 21629277 DOI: 10.1038/nrd3461  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2011 Collins FS. Genome-sequencing anniversary. Faces of the genome. Science (New York, N.Y.). 331: 546. PMID 21292963 DOI: 10.1126/science.1202894  0.96
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  0.96
2011 Collins FS. Inside the National Institutes of Health Biopharm International. 24.  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2010 Hamburg MA, Collins FS. The path to personalized medicine New England Journal of Medicine. 363: 301-304. PMID 20551152 DOI: 10.1056/NEJMp1006304  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2010 Collins FS. Opportunities for research and NIH Science. 327: 36-37. PMID 20044560 DOI: 10.1126/science.1185055  0.96
2009 Rosenfeld MA, Collins FS. Gene therapy for cystic fibrosis. 1996 Chest. 136. PMID 20162780  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2008 Collins FS. Retrospective: Victor A. McKusick (1921-2008) Science (New York, N.Y.). 321: 925. PMID 18703732  0.96
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  0.96
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  0.96
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  0.96
2008 Collins FS, Gray GM, Bucher JR. Transforming environmental health protection Science. 319: 906-907. PMID 18276874 DOI: 10.1126/science.1154619  0.96
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  0.96
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  0.96
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  0.96
2008 Merideth MA, Collins FS, Gahl WA. The authors reply New England Journal of Medicine. 358: 2410-2411.  0.96
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  0.96
2007 Lowrance WW, Collins FS. Identifiability in genomic research Science. 317: 600-602. PMID 17673640 DOI: 10.1126/science.1147699  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2007 Collins FS, Barker AD. Mapping the cancer genome Scientific American. 296: 50-57. PMID 17348159  0.96
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  0.96
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  0.96
2007 Collins FS, Manolio TA. Merging and emerging cohorts: necessary but not sufficient. Nature. 445: 259. PMID 17230172 DOI: 10.1038/445259a  0.96
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  0.96
2006 Capell BC, Collins FS. Human laminopathies: Nuclei gone genetically awry Nature Reviews Genetics. 7: 940-952. PMID 17139325 DOI: 10.1038/nrg1906  0.96
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  0.96
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  0.96
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  0.96
2006 Collins FS. No longer just looking under the lamppost American Journal of Human Genetics. 79: 421-426. PMID 16909378 DOI: 10.1086/507611  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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: 10.1034/ng1436  0.96
2004 Collins FS. An audience with...Francis S. Collins [interview] Nature Reviews. Drug Discovery. 3: 640. PMID 15317147  0.96
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  0.96
2004 Collins FS. Francis S. Collins Nature Reviews Drug Discovery. 3: 640.  0.96
2003 Collins FS. Genome research: The next generation Cold Spring Harbor Symposia On Quantitative Biology. 68: 49-54. PMID 15338602  0.96
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  0.96
2003 Albin RL. Genomic medicine. The New England Journal of Medicine. 349: 2170-1; author reply. PMID 14645650 DOI: 10.1056/NEJM200311273492219  0.96
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  0.96
2003 Baxevanis AD, Collins FS. Power to the people. A User's Guide to the Human Genome. Foreward Nature Genetics. 35: 2. PMID 14578888  0.96
2003 Guttmacher AE, Collins FS. Welcome to the genomic era New England Journal of Medicine. 349: 996-998. PMID 12954750 DOI: 10.1056/NEJMe038132  0.96
2003 Patenaude AF, Guttmacher AE, Collins FS. Psychologists' Contributions to the Genetic Revolution American Psychologist. 58: 319-320. PMID 12866400  0.96
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  0.96
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  0.96
2003 Insel TR, Collins FS. Psychiatry in the genomics era. The American Journal of Psychiatry. 160: 616-20. PMID 12668345  0.96
2003 Grady PA, Collins FS. Genetics and nursing science: realizing the potential Nursing Research. 52: 69. PMID 12657981  0.96
2002 Guttmacher AE, Collins FS. Genomic medicine - A primer New England Journal of Medicine. 347: 1512-1520. PMID 12421895 DOI: 10.1056/NEJMra012240  0.96
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  0.96
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  0.96
2002 Guttmacher AE, Collins FS, Burke W. Genomic medicine: Genetic testing New England Journal of Medicine. 347: 1867-1875. DOI: 10.1056/NEJMoa012113  0.96
2002 Baxevanis AD, Collins FS. Power to the people Nature Genetics. 32: 2. DOI: 10.1038/ng962  0.96
2001 Collins FS, Guttmacher AE. Genetics moves into the medical mainstream Journal of the American Medical Association. 286: 2322-2324. PMID 11710899  0.96
2001 Collins FS. Contemplating the end of the beginning Genome Research. 11: 641-643. PMID 11337461 DOI: 10.1101/gr.189801  0.96
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  0.96
2001 Collins FS, McKusick VA. Implications of the Human Genome Project for medical science. Jama. 285: 540-4. PMID 11176855  0.96
2001 Collins FS, Mansoura MK. The human genome project: Revealing the shared inheritance of all humankind Cancer. 91: 221-225. PMID 11148583  0.96
2000 Guttmacher AE, Collins FS. Genetics resources on the Web (GROW) Genetics in Medicine. 2: 296-299.  0.96
1999 Collins FS, Jegalian KG. Deciphering the Code of Life Scientific American. 281: 86-91. PMID 10614070  0.96
1999 Hacia JG, Collins FS. Mutational analysis using oligonucleotide microarrays Journal of Medical Genetics. 36: 730-736. PMID 10528850  0.96
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  0.96
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  0.96
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  0.96
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  0.96
1999 Collins FS. Genetics: An explosion of knowledge is transforming clinical practice Geriatrics. 54: 41-47. PMID 9934355  0.96
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  0.96
1999 Collins FS. Microarrays and macroconsequences Nature Genetics. 21: 2-2. DOI: 10.1038/4425  0.96
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  0.96
1998 Hacia JG, Brody LC, Collins FS. Applications of DNA chips for genomic analysis Molecular Psychiatry. 3: 483-492. PMID 9857973  0.96
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  0.96
1998 Hacia JG, Brody LC, Collins FS. New approaches to BRCA1 mutation detection Breast Disease. 10: 45-59.  0.96
1997 Kahn MJ, Jamison KR, Collins FS. Protecting our 'family secrets' The Washington Post. A15. PMID 11647280  0.96
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  0.96
1997 Collins FS. Preparing health professionals for the genetic revolution Journal of the American Medical Association. 278: 1285-1286. PMID 9333274  0.96
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  0.96
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  0.96
1997 Collins FS. Sequencing the human genome Hospital Practice. 32.  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
1996 Jordan E, Collins FS. A march of genetic maps Nature. 380: 111-112. PMID 8600381 DOI: 10.1038/380111a0  0.96
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  0.96
1996 Rosenfeld MA, Collins FS. Gene therapy for cystic fibrosis Chest. 109: 241-252. PMID 8549191  0.96
1996 Collins FS. BRCA1 - Lots of mutations, lots of dilemmas New England Journal of Medicine. 334: 186-188. PMID 8531977 DOI: 10.1056/NEJM199601183340311  0.96
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  0.96
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  0.96
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  0.96
1995 Collins FS. Positional cloning moves from perditional to traditional Nature Genetics. 9: 347-350. PMID 7795639 DOI: 10.1038/ng0495-347  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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-#  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
1994 Collins FS. Response [2] Science. 264: 13-14. DOI: 10.1126/science.334.6058.903  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.32
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  0.96
1993 Chandrasekharappa SC, King SE, Freedman ML, Hayes ST, Bowcock AM, Collins FS. The CA repeat marker D17S791 is located within 40 kb of the WNT3 gene on chromosome 17q. Genomics. 18: 728-9. PMID 8307586 DOI: 10.1016/S0888-7543(05)80386-6  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.32
1993 Drumm ML, Collins FS. Molecular biology of cystic fibrosis Molecular Genetic Medicine. 3: 33-68. PMID 7693108  0.96
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  0.96
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  0.96
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  0.96
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  0.96
1993 Sferra TJ, Collins FS. The molecular biology of cystic fibrosis Annual Review of Medicine. 44: 133-144. PMID 7682803  0.96
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  0.96
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  0.32
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  0.32
1992 Gutmann DH, Collins FS. Recent progress toward understanding the molecular biology of von Recklinghausen neurofibromatosis Annals of Neurology. 31: 555-561. PMID 1596091  0.96
1992 Wilson JM, Collins FS. More from the modellers Nature. 359: 195-196. PMID 1528259  0.96
1992 Collins FS, Wilson JM. A welcome animal model Nature. 358: 708-709. PMID 1508266  0.96
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  0.32
1992 Collins FS. Cystic fibrosis: Molecular biology and therapeutic implications Science. 256: 774-779. PMID 1375392  0.96
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  0.32
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  0.32
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  0.96
1992 Collins FS. Positional cloning: Let’s not call it reverse anymore Nature Genetics. 1: 3-6. PMID 1301996 DOI: 10.1038/ng0492-3  0.96
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  0.96
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  0.96
1991 Collins FS. The Genome Project and human health Faseb Journal. 5: 77. PMID 1991592  0.96
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  0.96
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  0.96
1991 Collins FS. Identification of disease genes: Recent successes Hospital Practice. 26: 93-98. PMID 1918209  0.96
1991 Collins FS. Medical and ethical consequences of the human genome project The Journal of Clinical Ethics. 2: 260-267. PMID 1804396  0.96
1991 Wallace MR, Collins FS. Molecular genetics of von Recklinghausen neurofibromatosis Advances in Human Genetics. 20: 267-307. PMID 1801591  0.96
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  0.96
1991 Collins FS. Of needles and haystacks: finding human disease genes by positional cloning Clinical Research. 39: 615-623. PMID 1764889  0.96
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  0.96
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  0.32
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  0.96
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  0.96
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  0.96
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  0.96
1990 Collins FS. Identifying human disease genes by positional cloning Harvey Lectures. 86: 149-164. PMID 2152136  0.96
1990 Collins FS, Riordan JR, Tsui LC. The cystic fibrosis gene: Isolation and significance Hospital Practice. 25: 47-57. PMID 1698801  0.96
1990 Iannuzzi MC, Collins FS. Reverse genetics and cystic fibrosis American Journal of Respiratory Cell and Molecular Biology. 2: 309-316. PMID 1691007  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
1987 Treisman J, Collins FS. Adult Turner syndrome associated with chylous ascites and vascular anomalies. Clinical Genetics. 31: 218-23. PMID 3594929  0.96
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/15.14.5909  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
1984 Collins FS, Weissman SM. The molecular genetics of human hemoglobin Progress in Nucleic Acid Research and Molecular Biology. 31: 315-462. PMID 6397774  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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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