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Donald F Conrad

Showing results (71-80 of 106) with videos related to

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Nature Communications|October 13, 2019
Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertilityArthur S Lee, Jannette Rusch, Ana C Lima, et al.
Molecular Biology and Evolution|February 18, 2009
Haplotypic background of a private allele at high frequency in the AmericasKari B Schroeder, Mattias Jakobsson, Michael H Crawford, et al.
Nature Genetics|June 14, 2011
Variation in genome-wide mutation rates within and between human familiesDonald F Conrad, Jonathan E M Keebler, Mark A DePristo, et al.
Human Genetics|November 8, 2011
Exploration of signals of positive selection derived from genotype-based human genome scans using re-sequencing dataMin Hu, Qasim Ayub, José Afonso Guerra-Assunção, et al.
Biorxiv : the Preprint Server for Biology|January 23, 2024
Taking identity-by-descent analysis into the wild: Estimating realized relatedness in free-ranging macaquesAnnika Freudiger, Vladimir M Jovanovic, Yilei Huang, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 14, 2025
Estimating realized relatedness in free-ranging macaques by inferring identity-by-descent segmentsAnnika Freudiger, Vladimir M Jovanovic, Yilei Huang, et al.
Frontiers in Genetics|October 13, 2025
A partially automated method for DNA extraction from marmoset hair follicles to avoid blood chimerismAlexandra M Stendahl, Qiangge Zhang, Ana C Lima, et al.
Molecular Cell|February 15, 2024
C19ORF84 connects piRNA and DNA methylation machineries to defend the mammalian germ lineAnsgar Zoch, Gabriela Konieczny, Tania Auchynnikava, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2020
Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic menCsilla Krausz, Antoni Riera-Escamilla, Daniel Moreno-Mendoza, et al.
The New England Journal of Medicine|August 4, 2021
Variant <i>PNLDC1</i>, Defective piRNA Processing, and AzoospermiaLiina Nagirnaja, Nina Mørup, John E Nielsen, et al.
Pageof 11

Showing results (71-80 of 106) with videos related to

Sort By:
Pageof 11
Nature Communications|October 13, 2019
Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertilityArthur S Lee, Jannette Rusch, Ana C Lima, et al.
Molecular Biology and Evolution|February 18, 2009
Haplotypic background of a private allele at high frequency in the AmericasKari B Schroeder, Mattias Jakobsson, Michael H Crawford, et al.
Nature Genetics|June 14, 2011
Variation in genome-wide mutation rates within and between human familiesDonald F Conrad, Jonathan E M Keebler, Mark A DePristo, et al.
Human Genetics|November 8, 2011
Exploration of signals of positive selection derived from genotype-based human genome scans using re-sequencing dataMin Hu, Qasim Ayub, José Afonso Guerra-Assunção, et al.
Biorxiv : the Preprint Server for Biology|January 23, 2024
Taking identity-by-descent analysis into the wild: Estimating realized relatedness in free-ranging macaquesAnnika Freudiger, Vladimir M Jovanovic, Yilei Huang, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 14, 2025
Estimating realized relatedness in free-ranging macaques by inferring identity-by-descent segmentsAnnika Freudiger, Vladimir M Jovanovic, Yilei Huang, et al.
Frontiers in Genetics|October 13, 2025
A partially automated method for DNA extraction from marmoset hair follicles to avoid blood chimerismAlexandra M Stendahl, Qiangge Zhang, Ana C Lima, et al.
Molecular Cell|February 15, 2024
C19ORF84 connects piRNA and DNA methylation machineries to defend the mammalian germ lineAnsgar Zoch, Gabriela Konieczny, Tania Auchynnikava, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2020
Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic menCsilla Krausz, Antoni Riera-Escamilla, Daniel Moreno-Mendoza, et al.
The New England Journal of Medicine|August 4, 2021
Variant <i>PNLDC1</i>, Defective piRNA Processing, and AzoospermiaLiina Nagirnaja, Nina Mørup, John E Nielsen, et al.
Pageof 11