Chad Huff
Chad Huff
Assistant Professor of Epidemiology, MD Anderson Cancer Center
כתובת אימייל מאומתת בדומיין mdanderson.org - דף הבית
כותרת
צוטט על ידי
צוטט על ידי
שנה
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), 30-35, 2010
22672010
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
11492010
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
10192010
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
3292012
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
3262009
A genetic mechanism for Tibetan high-altitude adaptation
FR Lorenzo, C Huff, M Myllymäki, B Olenchock, S Swierczek, T Tashi, ...
Nature genetics 46 (9), 951-956, 2014
3132014
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), e1002236, 2011
2702011
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
2342013
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
2322011
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
2312011
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
1512014
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
1402013
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
1332011
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), 663-669, 2014
962014
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
842010
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
802012
Early history of Neanderthals and Denisovans
AR Rogers, RJ Bohlender, CD Huff
Proceedings of the National Academy of Sciences 114 (37), 9859-9863, 2017
772017
Variant annotation, analysis and selection tool
MG Reese, M Yandell, C Huff, H Hu, M Moore
US Patent App. 13/822,242, 2013
732013
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry …
MCY Ng, M Graff, Y Lu, AE Justice, P Mudgal, CT Liu, K Young, LR Yanek, ...
PLoS genetics 13 (4), e1006719, 2017
642017
Linkage disequilibrium between loci with unknown phase
AR Rogers, C Huff
Genetics 182 (3), 839-844, 2009
632009
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מאמרים 1–20