| Exome sequencing identifies the cause of a mendelian disorder SB Ng, KJ Buckingham, C Lee, AW Bigham, HK Tabor, KM Dent, CD Huff, ... Nature genetics 42 (1), 30, 2010 | 2101 | 2010 |
| Analysis of genetic inheritance in a family quartet by whole-genome sequencing JC Roach, G Glusman, AFA Smit, CD Huff, R Hubley, PT Shannon, ... Science 328 (5978), 636-639, 2010 | 1058 | 2010 |
| Genetic evidence for high-altitude adaptation in Tibet TS Simonson, Y Yang, CD Huff, H Yun, G Qin, DJ Witherspoon, Z Bai, ... Science 329 (5987), 72-75, 2010 | 863 | 2010 |
| Mobile elements create structural variation: analysis of a complete human genome J Xing, Y Zhang, K Han, AH Salem, SK Sen, CD Huff, Q Zhou, EF Kirkness, ... Genome research 19 (9), 1516-1526, 2009 | 295 | 2009 |
| De novo mutations in ATP1A3 cause alternating hemiplegia of childhood EL Heinzen, KJ Swoboda, Y Hitomi, F Gurrieri, S Nicole, B de Vries, ... Nature genetics 44 (9), 1030-1034, 2012 | 279 | 2012 |
| A comprehensive map of mobile element insertion polymorphisms in humans C Stewart, D Kural, MP Strömberg, JA Walker, MK Konkel, AM Stütz, ... PLoS genetics 7 (8), 2011 | 238 | 2011 |
| A genetic mechanism for Tibetan high-altitude adaptation FR Lorenzo, C Huff, M Myllymäki, B Olenchock, S Swierczek, T Tashi, ... Nature genetics 46 (9), 951, 2014 | 236 | 2014 |
| A probabilistic disease-gene finder for personal genomes M Yandell, C Huff, H Hu, M Singleton, B Moore, J Xing, LB Jorde, ... Genome research 21 (9), 1529-1542, 2011 | 223 | 2011 |
| Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency AF Rope, K Wang, R Evjenth, J Xing, JJ Johnston, JJ Swensen, ... The American Journal of Human Genetics 89 (1), 28-43, 2011 | 201 | 2011 |
| Genomic diversity and evolution of the head crest in the rock pigeon MD Shapiro, Z Kronenberg, C Li, ET Domyan, H Pan, M Campbell, H Tan, ... Science 339 (6123), 1063-1067, 2013 | 185 | 2013 |
| VAAST 2.0: Improved variant classification and disease‐gene identification using a conservation‐controlled amino acid substitution matrix H Hu, CD Huff, B Moore, S Flygare, MG Reese, M Yandell Genetic epidemiology 37 (6), 622-634, 2013 | 123 | 2013 |
| Maximum-likelihood estimation of recent shared ancestry (ERSA) CD Huff, DJ Witherspoon, TS Simonson, J Xing, WS Watkins, Y Zhang, ... Genome research 21 (5), 768-774, 2011 | 119 | 2011 |
| Phevor combines multiple biomedical ontologies for accurate identification of disease-causing alleles in single individuals and small nuclear families MV Singleton, SL Guthery, KV Voelkerding, K Chen, B Kennedy, ... The American Journal of Human Genetics 94 (4), 599-610, 2014 | 118 | 2014 |
| A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data H Hu, JC Roach, H Coon, SL Guthery, KV Voelkerding, RL Margraf, ... Nature biotechnology 32 (7), 663, 2014 | 87 | 2014 |
| Toward a more uniform sampling of human genetic diversity: a survey of worldwide populations by high-density genotyping J Xing, WS Watkins, A Shlien, E Walker, CD Huff, DJ Witherspoon, ... Genomics 96 (4), 199-210, 2010 | 76 | 2010 |
| Metabolic insight into mechanisms of high-altitude adaptation in Tibetans RL Ge, TS Simonson, RC Cooksey, U Tanna, G Qin, CD Huff, ... Molecular genetics and metabolism 106 (2), 244-247, 2012 | 68 | 2012 |
| Variant annotation, analysis and selection tool MG Reese, M Yandell, C Huff, H Hu, M Moore US Patent App. 13/822,242, 2013 | 58 | 2013 |
| Genetic diversity in India and the inference of Eurasian population expansion J Xing, WS Watkins, Y Hu, CD Huff, A Sabo, DM Muzny, MJ Bamshad, ... Genome biology 11 (11), R113, 2010 | 57 | 2010 |
| Linkage disequilibrium between loci with unknown phase AR Rogers, C Huff Genetics 182 (3), 839-844, 2009 | 55 | 2009 |
| Crohn’s disease and genetic hitchhiking at IBD5 CD Huff, DJ Witherspoon, Y Zhang, C Gatenbee, LA Denson, ... Molecular biology and evolution 29 (1), 101-111, 2012 | 52 | 2012 |
