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Mark D Fleming

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American Journal of Human Genetics|April 2, 2024

Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic diseaseGabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.

Medrxiv : the Preprint Server for Health Sciences|October 24, 2023

Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic diseaseGabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.

HGG Advances|January 20, 2022

Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disordersMichael A Levy, Haley McConkey, Jennifer Kerkhof, et al.

Human Mutation|July 29, 2022

Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disordersMichael A Levy, Raissa Relator, Haley McConkey, et al.

Diabetes|September 23, 2010

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathwaysNicole Soranzo, Serena Sanna, Eleanor Wheeler, et al.

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Search research articles

Showing results (211-220 of 215) with videos related to

Sort By:

Pageof 22

You have reached the last page of results.This site can display upto 215 results.

American Journal of Human Genetics|April 2, 2024

Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic diseaseGabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.

Medrxiv : the Preprint Server for Health Sciences|October 24, 2023

Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic diseaseGabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.

HGG Advances|January 20, 2022

Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disordersMichael A Levy, Haley McConkey, Jennifer Kerkhof, et al.

Human Mutation|July 29, 2022

Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disordersMichael A Levy, Raissa Relator, Haley McConkey, et al.

Diabetes|September 23, 2010

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathwaysNicole Soranzo, Serena Sanna, Eleanor Wheeler, et al.

Pageof 22