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Saharon Rosset

Showing results (41-50 of 64) with videos related to

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American Journal of Human Genetics|June 4, 2016
Fast and Accurate Construction of Confidence Intervals for HeritabilityRegev Schweiger, Shachar Kaufman, Reijo Laaksonen, et al.
Genetics|September 16, 2008
Maximum-likelihood estimation of site-specific mutation rates in human mitochondrial DNA from partial phylogenetic classificationSaharon Rosset, R Spencer Wells, David F Soria-Hernanz, et al.
Infection|October 29, 2024
Characterizing CRP dynamics during acute infectionsStacey S Cherny, Rafael Y Brzezinski, Asaf Wasserman, et al.
Genetics|October 14, 2017
RL-SKAT: An Exact and Efficient Score Test for Heritability and Set TestsRegev Schweiger, Omer Weissbrod, Elior Rahmani, et al.
Nature Communications|August 2, 2019
Cell-type-specific resolution epigenetics without the need for cell sorting or single-cell biologyElior Rahmani, Regev Schweiger, Brooke Rhead, et al.
Nature Communications|November 23, 2018
Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-testsRegev Schweiger, Eyal Fisher, Omer Weissbrod, et al.
American Journal of Human Genetics|April 10, 2012
A "Copernican" reassessment of the human mitochondrial DNA tree from its rootDoron M Behar, Mannis van Oven, Saharon Rosset, et al.
Parkinsonism & Related Disorders|June 19, 2012
Dyskinesias in patients with Parkinson's disease: effect of the leucine-rich repeat kinase 2 (LRRK2) G2019S mutationGilad Yahalom, Natalie Kaplan, Aya Vituri, et al.
Human Genetics|August 12, 2009
Extended Y chromosome haplotypes resolve multiple and unique lineages of the Jewish priesthoodMichael F Hammer, Doron M Behar, Tatiana M Karafet, et al.
Human Genetics|July 17, 2010
Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 geneShay Tzur, Saharon Rosset, Revital Shemer, et al.
Pageof 7

Showing results (41-50 of 64) with videos related to

Sort By:
Pageof 7
American Journal of Human Genetics|June 4, 2016
Fast and Accurate Construction of Confidence Intervals for HeritabilityRegev Schweiger, Shachar Kaufman, Reijo Laaksonen, et al.
Genetics|September 16, 2008
Maximum-likelihood estimation of site-specific mutation rates in human mitochondrial DNA from partial phylogenetic classificationSaharon Rosset, R Spencer Wells, David F Soria-Hernanz, et al.
Infection|October 29, 2024
Characterizing CRP dynamics during acute infectionsStacey S Cherny, Rafael Y Brzezinski, Asaf Wasserman, et al.
Genetics|October 14, 2017
RL-SKAT: An Exact and Efficient Score Test for Heritability and Set TestsRegev Schweiger, Omer Weissbrod, Elior Rahmani, et al.
Nature Communications|August 2, 2019
Cell-type-specific resolution epigenetics without the need for cell sorting or single-cell biologyElior Rahmani, Regev Schweiger, Brooke Rhead, et al.
Nature Communications|November 23, 2018
Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-testsRegev Schweiger, Eyal Fisher, Omer Weissbrod, et al.
American Journal of Human Genetics|April 10, 2012
A "Copernican" reassessment of the human mitochondrial DNA tree from its rootDoron M Behar, Mannis van Oven, Saharon Rosset, et al.
Parkinsonism & Related Disorders|June 19, 2012
Dyskinesias in patients with Parkinson's disease: effect of the leucine-rich repeat kinase 2 (LRRK2) G2019S mutationGilad Yahalom, Natalie Kaplan, Aya Vituri, et al.
Human Genetics|August 12, 2009
Extended Y chromosome haplotypes resolve multiple and unique lineages of the Jewish priesthoodMichael F Hammer, Doron M Behar, Tatiana M Karafet, et al.
Human Genetics|July 17, 2010
Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 geneShay Tzur, Saharon Rosset, Revital Shemer, et al.
Pageof 7