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/vufind/Search/Results?lookfor=%22Lange%2C+Ethan+M.%22&type=Person&page=5
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PubPharm (260)
41
A robust and powerful two-step testing procedure for local ancestry adjusted allelic association analysis in admixed populations
enthalten in:
Genetic epidemiology
| 2018
von
Duan, Q.
|
Xu, Z.
|
Raffield, L.
| +5
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42
Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey
enthalten in:
PLoS genetics
| 2018
von
Spracklen, C.
|
Shi, J.
|
Vadlamudi, S.
| +18
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43
Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults study
enthalten in:
Journal of human genetics
| 2018
von
Raffield, L.
|
Ellis, J.
|
Olson, N.
| +16
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44
Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease
enthalten in:
PLoS genetics
| 2018
von
Raffield, L.
|
Ulirsch, J.
|
Naik, R.
| +23
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45
D-Dimer in African Americans : Whole Genome Sequence Analysis and Relationship to Cardiovascular Disease Risk in the Jackson Heart Study
enthalten in:
Arteriosclerosis, thrombosis, and vascular biology
| 2017
von
Raffield, L.
|
Zakai, N.
|
Duan, Q.
| +23
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46
D-Dimer in African Americans: Whole Genome Sequence Analysis and Relationship to Cardiovascular Disease Risk in the Jackson Heart Study
enthalten in:
Arteriosclerosis, thrombosis, and vascular biology
| 2017
von
Raffield, L.
|
Zakai, N.
|
Duan, Q.
| +22
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47
REVEL : An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants
enthalten in:
American journal of human genetics
| 2016
von
Ioannidis, N.
|
Rothstein, J.
|
Pejaver, V.
| +38
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48
Evidence for Association between SH2B1 Gene Variants and Glycated Hemoglobin in Nondiabetic European American Young Adults : The Add Health Study
enthalten in:
Annals of human genetics
| 2016
von
Lange, L.
|
Graff, M.
|
Lange, E.
| +6
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49
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21
enthalten in:
Human genetics
| 2016
von
Teerlink, C.
|
Leongamornlert, D.
|
Dadaev, T.
| +40
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50
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21
enthalten in:
Human genetics
| 2016
von
Teerlink, C.
|
Leongamornlert, D.
|
Dadaev, T.
| +38
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