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Donald F Conrad

Showing results (91-100 of 106) with videos related to

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Human Genetics|May 8, 2021
Variants in GCNA, X-linked germ-cell genome integrity gene, identified in men with primary spermatogenic failureJimmaline J Hardy, Margot J Wyrwoll, William Mcfadden, et al.
Frontiers in Endocrinology|April 24, 2024
Undiagnosed RASopathies in infertile menAnna-Grete Juchnewitsch, Kristjan Pomm, Avirup Dutta, et al.
Nature|October 13, 2017
Dynamic landscape and regulation of RNA editing in mammalsMeng How Tan, Qin Li, Raghuvaran Shanmugam, et al.
Nature Communications|August 9, 2024
Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertilityBirgit Stallmeyer, Clara Bühlmann, Rytis Stakaitis, et al.
Human Molecular Genetics|July 23, 2015
Low-frequency germline variants across 6p22.2-6p21.33 are associated with non-obstructive azoospermia in Han Chinese menBixian Ni, Yuan Lin, Liangdan Sun, et al.
Biological Psychiatry|July 23, 2013
Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophreniaJennifer Gladys Mulle, Ann E Pulver, John A McGrath, et al.
American Journal of Human Genetics|July 17, 2020
Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male InfertilityMargot J Wyrwoll, Şehime G Temel, Liina Nagirnaja, et al.
Science (New York, N.Y.)|May 9, 2015
Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptomeManuel A Rivas, Matti Pirinen, Donald F Conrad, et al.
Biorxiv : the Preprint Server for Biology|April 3, 2026
A Complete Genome for the Common MarmosetPrajna Hebbar, Tamara Potapova, Hailey Loucks, et al.
Nature|November 24, 2006
Global variation in copy number in the human genomeRichard Redon, Shumpei Ishikawa, Karen R Fitch, et al.
Pageof 11

Showing results (91-100 of 106) with videos related to

Sort By:
Pageof 11
Human Genetics|May 8, 2021
Variants in GCNA, X-linked germ-cell genome integrity gene, identified in men with primary spermatogenic failureJimmaline J Hardy, Margot J Wyrwoll, William Mcfadden, et al.
Frontiers in Endocrinology|April 24, 2024
Undiagnosed RASopathies in infertile menAnna-Grete Juchnewitsch, Kristjan Pomm, Avirup Dutta, et al.
Nature|October 13, 2017
Dynamic landscape and regulation of RNA editing in mammalsMeng How Tan, Qin Li, Raghuvaran Shanmugam, et al.
Nature Communications|August 9, 2024
Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertilityBirgit Stallmeyer, Clara Bühlmann, Rytis Stakaitis, et al.
Human Molecular Genetics|July 23, 2015
Low-frequency germline variants across 6p22.2-6p21.33 are associated with non-obstructive azoospermia in Han Chinese menBixian Ni, Yuan Lin, Liangdan Sun, et al.
Biological Psychiatry|July 23, 2013
Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophreniaJennifer Gladys Mulle, Ann E Pulver, John A McGrath, et al.
American Journal of Human Genetics|July 17, 2020
Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male InfertilityMargot J Wyrwoll, Şehime G Temel, Liina Nagirnaja, et al.
Science (New York, N.Y.)|May 9, 2015
Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptomeManuel A Rivas, Matti Pirinen, Donald F Conrad, et al.
Biorxiv : the Preprint Server for Biology|April 3, 2026
A Complete Genome for the Common MarmosetPrajna Hebbar, Tamara Potapova, Hailey Loucks, et al.
Nature|November 24, 2006
Global variation in copy number in the human genomeRichard Redon, Shumpei Ishikawa, Karen R Fitch, et al.
Pageof 11