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Jeremy McRae

Showing results (1-10 of 18) with videos related to

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Biorxiv : the Preprint Server for Biology|February 14, 2024
Highly parameterized polygenic scores tend to overfit to population stratification via random effectsAlan J Aw, Jeremy McRae, Elior Rahmani, et al.
Nature|May 11, 2022
Genetic and chemotherapeutic influences on germline hypermutationJoanna Kaplanis, Benjamin Ide, Rashesh Sanghvi, et al.
Nature|November 12, 2025
Estimation and mapping of the missing heritability of human phenotypesPierrick Wainschtein, Yuanxiang Zhang, Jeremy Schwartzentruber, et al.
American Journal of Human Genetics|October 15, 2019
Finding Diagnostically Useful Patterns in Quantitative Phenotypic DataStuart Aitken, Helen V Firth, Jeremy McRae, et al.
Nature|September 28, 2018
Common genetic variants contribute to risk of rare severe neurodevelopmental disordersMari E K Niemi, Hilary C Martin, Daniel L Rice, et al.
Nature Communications|January 28, 2021
The contribution of X-linked coding variation to severe developmental disordersHilary C Martin, Eugene J Gardner, Kaitlin E Samocha, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2023
Rare penetrant mutations confer severe risk of common diseasesPetko Fiziev, Jeremy McRae, Jacob C Ulirsch, et al.
Science (New York, N.Y.)|June 1, 2023
Rare penetrant mutations confer severe risk of common diseasesPetko P Fiziev, Jeremy McRae, Jacob C Ulirsch, et al.
American Journal of Human Genetics|August 23, 2016
Biallelic Variants in UBA5 Link Dysfunctional UFM1 Ubiquitin-like Modifier Pathway to Severe Infantile-Onset EncephalopathyMikko Muona, Ryosuke Ishimura, Anni Laari, et al.
American Journal of Human Genetics|July 26, 2016
BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates TranscriptionCristina Dias, Sara B Estruch, Sarah A Graham, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Biorxiv : the Preprint Server for Biology|February 14, 2024
Highly parameterized polygenic scores tend to overfit to population stratification via random effectsAlan J Aw, Jeremy McRae, Elior Rahmani, et al.
Nature|May 11, 2022
Genetic and chemotherapeutic influences on germline hypermutationJoanna Kaplanis, Benjamin Ide, Rashesh Sanghvi, et al.
Nature|November 12, 2025
Estimation and mapping of the missing heritability of human phenotypesPierrick Wainschtein, Yuanxiang Zhang, Jeremy Schwartzentruber, et al.
American Journal of Human Genetics|October 15, 2019
Finding Diagnostically Useful Patterns in Quantitative Phenotypic DataStuart Aitken, Helen V Firth, Jeremy McRae, et al.
Nature|September 28, 2018
Common genetic variants contribute to risk of rare severe neurodevelopmental disordersMari E K Niemi, Hilary C Martin, Daniel L Rice, et al.
Nature Communications|January 28, 2021
The contribution of X-linked coding variation to severe developmental disordersHilary C Martin, Eugene J Gardner, Kaitlin E Samocha, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2023
Rare penetrant mutations confer severe risk of common diseasesPetko Fiziev, Jeremy McRae, Jacob C Ulirsch, et al.
Science (New York, N.Y.)|June 1, 2023
Rare penetrant mutations confer severe risk of common diseasesPetko P Fiziev, Jeremy McRae, Jacob C Ulirsch, et al.
American Journal of Human Genetics|August 23, 2016
Biallelic Variants in UBA5 Link Dysfunctional UFM1 Ubiquitin-like Modifier Pathway to Severe Infantile-Onset EncephalopathyMikko Muona, Ryosuke Ishimura, Anni Laari, et al.
American Journal of Human Genetics|July 26, 2016
BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates TranscriptionCristina Dias, Sara B Estruch, Sarah A Graham, et al.
Pageof 2