| 1 3 Whole-Genome Genotyping SB Gabriel, MP Weiner Genetic Variation: A Laboratory Manual, 213, 2007 | | 2007 |
| 1: Novarino G, Fenstermaker AG, Zaki MS, Hofree M, Silhavy JL, Heiberg AD, Abdellateef M, Rosti B, Scott E, Mansour L, Masri A, Kayserili H, Al-Aama JY, Abdel-Salam GMH … RO Rosti, N Akizu, KK Vaux, A Johansen, AA Koh, H Megahed, A Durr, ... | | |
| 1. Cohort demographics G Lettre, CD Palmer, T Young, KG Ejebe, H Allayee, EJ Benjamin, ... | | |
| 115 IDENTIFICATION OF SUSCEPTIBILITY LOCI FOR THE LOW HDLC/CHD TRAIT M Brousseau, S Demissie, G Peloso, L Cupples, S Gabriel, D Collins, ... Atherosclerosis Supplements 10 (2), e49, 2009 | | 2009 |
| 1314 RECURRENT MUTATIONS IN SPOP DEFINE A DISTINCT MOLECULAR CLASS OF PROSTATE CANCER C Barbieri, S Baca, F Demichelis, M Lawrence, M Blattner, JP Theurillat, ... The Journal of Urology 4 (187), e532-e533, 2012 | | 2012 |
| 716 PROGNOSTIC GENE-EXPRESSION SIGNATURE FOR HEPATITIS C-RELATED EARLY-STAGE LIVER CIRRHOSIS Y Hoshida, A Villanueva, A Sangiovanni, M Solé, C Hur, KL Andersson, ... Journal of Hepatology 56, S283, 2012 | | 2012 |
| 7th Annual European Antibody Congress 2011: November 29–December 1, 2011, Geneva, Switzerland AA Lugovskoy, JM Reichert, A Beck mabs 4 (2), 134, 2012 | 6 | 2012 |
| A 4-arm randomized controlled pilot trial of innovative solutions for jugular central venous access device securement in 221 cardiac surgical patients CM Rickard, M Edwards, AJ Spooner, G Mihala, N Marsh, J Best, T Wendt, ... Journal of critical care 36, 35-42, 2016 | 24 | 2016 |
| A comprehensive pan-cancer molecular study of gynecologic and breast cancers AC Berger, A Korkut, RS Kanchi, AM Hegde, W Lenoir, W Liu, Y Liu, ... Cancer cell 33 (4), 690-705. e9, 2018 | 87 | 2018 |
| A Cryptic Intronic GATA1 Splicing Mutation Provides Insights Into Human Hematopoietic Differentiation N Abdulhay, J Verboon, J Ulirsch, B Zieger, X Mi, E Obeng, M Erlacher, ... Experimental Hematology 64, S53, 2018 | | 2018 |
| A dominant mutation in human RAD51 reveals its function in DNA interstrand crosslink repair independent of homologous recombination AT Wang, T Kim, JE Wagner, BA Conti, FP Lach, AL Huang, H Molina, ... Molecular cell 59 (3), 478-490, 2015 | 162 | 2015 |
| A four-arm randomised controlled pilot trial of innovative solutions for jugular central venous access device securement in 221 cardiac surgical patients CM Rickard, M Edwards, AJ Spooner, G Mihala, N Marsh, J Best, T Wendt, ... | | |
| A framework for the interpretation of de novo mutation in human disease KE Samocha, EB Robinson, SJ Sanders, C Stevens, A Sabo, LM McGrath, ... Nature genetics 46 (9), 944, 2014 | 590 | 2014 |
| A framework for variation discovery and genotyping using next-generation DNA sequencing data MA DePristo, E Banks, R Poplin, KV Garimella, JR Maguire, C Hartl, ... Nature genetics 43 (5), 491, 2011 | 6776 | 2011 |
| A functional landscape of resistance to ALK inhibition in lung cancer FH Wilson, CM Johannessen, F Piccioni, P Tamayo, JW Kim, ... Cancer cell 27 (3), 397-408, 2015 | 107 | 2015 |
| A genome-wide linkage and association scan reveals novel loci for autism LA Weiss, DE Arking, ... Nature 461 (7265), 802, 2009 | 614 | 2009 |
| A glimpse into the somatic mutation landscape of melanoma through exome sequencing of 121 tumor-normal pairs E Hodis, I Watson, JP Theurillat, L Zou, C Place, E Nickerson, D Auclair, ... Cancer Research 72 (8 Supplement), 5056-5056, 2012 | | 2012 |
| A global reference for human genetic variation JT Simpson, R Sudbrak, F Kahveci, CA Albers, SA Sinari, EV Ball, ... Nature Research, 2015 | | 2015 |
| A haplotype map of the human genome D Altshuler, P Donnelly, International HapMap Consortium Nature 437 (7063), 1299, 2005 | 1036 | 2005 |
| A homozygous missense mutation in HERC2 associated with global developmental delay and autism spectrum disorder EG Puffenberger, RN Jinks, H Wang, B Xin, C Fiorentini, EA Sherman, ... Human mutation 33 (12), 1639-1646, 2012 | 78 | 2012 |
