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Hilary C Martin

Showing results (51-60 of 68) with videos related to

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Nature|October 15, 2020
Evidence for 28 genetic disorders discovered by combining healthcare and research dataJoanna Kaplanis, Kaitlin E Samocha, Laurens Wiel, et al.
Nature Medicine|May 29, 2023
Polygenic prediction of preeclampsia and gestational hypertensionMichael C Honigberg, Buu Truong, Raiyan R Khan, et al.
Nature|September 11, 2024
Genetic links between ovarian ageing, cancer risk and de novo mutation ratesStasa Stankovic, Saleh Shekari, Qin Qin Huang, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
An ancestry-enriched HNF4A variant and GP2 reveal distinct mechanisms of type 2 diabetes in exome-wide study of 13,674 cases and 41,024 controlsSam Hodgson, Vi Bui, Siqi Hu, et al.
The Journal of Clinical Endocrinology and Metabolism|June 20, 2023
Prevalence of Deleterious Variants in MC3R in Patients With Constitutional Delay of Growth and PubertyKatie Duckett, Alice Williamson, John W R Kincaid, et al.
Science (New York, N.Y.)|November 10, 2018
Quantifying the contribution of recessive coding variation to developmental disordersHilary C Martin, Wendy D Jones, Rebecca McIntyre, et al.
American Journal of Human Genetics|May 3, 2016
Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female FertilityHamdi Mbarek, Stacy Steinberg, Dale R Nyholt, et al.
Nature|October 8, 2025
Somatic mutation and selection at population scaleAndrew R J Lawson, Federico Abascal, Pantelis A Nicola, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaborationDuncan S Palmer, Barney Hill, Sam Hodgson, et al.
Nature Genetics|March 28, 2026
Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosityHye In Kim, Christopher DeBoever, Klaudia Walter, et al.
Pageof 7

Showing results (51-60 of 68) with videos related to

Sort By:
Pageof 7
Nature|October 15, 2020
Evidence for 28 genetic disorders discovered by combining healthcare and research dataJoanna Kaplanis, Kaitlin E Samocha, Laurens Wiel, et al.
Nature Medicine|May 29, 2023
Polygenic prediction of preeclampsia and gestational hypertensionMichael C Honigberg, Buu Truong, Raiyan R Khan, et al.
Nature|September 11, 2024
Genetic links between ovarian ageing, cancer risk and de novo mutation ratesStasa Stankovic, Saleh Shekari, Qin Qin Huang, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
An ancestry-enriched HNF4A variant and GP2 reveal distinct mechanisms of type 2 diabetes in exome-wide study of 13,674 cases and 41,024 controlsSam Hodgson, Vi Bui, Siqi Hu, et al.
The Journal of Clinical Endocrinology and Metabolism|June 20, 2023
Prevalence of Deleterious Variants in MC3R in Patients With Constitutional Delay of Growth and PubertyKatie Duckett, Alice Williamson, John W R Kincaid, et al.
Science (New York, N.Y.)|November 10, 2018
Quantifying the contribution of recessive coding variation to developmental disordersHilary C Martin, Wendy D Jones, Rebecca McIntyre, et al.
American Journal of Human Genetics|May 3, 2016
Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female FertilityHamdi Mbarek, Stacy Steinberg, Dale R Nyholt, et al.
Nature|October 8, 2025
Somatic mutation and selection at population scaleAndrew R J Lawson, Federico Abascal, Pantelis A Nicola, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaborationDuncan S Palmer, Barney Hill, Sam Hodgson, et al.
Nature Genetics|March 28, 2026
Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosityHye In Kim, Christopher DeBoever, Klaudia Walter, et al.
Pageof 7