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Harrison Brand

Showing results (11-20 of 86) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|October 9, 2014
CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitorsAarathi Sugathan, Marta Biagioli, Christelle Golzio, et al.
Nature Genetics|January 24, 2024
Author Correction: GATK-gCNV enables the discovery of rare copy number variants from exome sequencing dataMehrtash Babadi, Jack M Fu, Samuel K Lee, et al.
Nature Genetics|August 21, 2023
GATK-gCNV enables the discovery of rare copy number variants from exome sequencing dataMehrtash Babadi, Jack M Fu, Samuel K Lee, et al.
The New England Journal of Medicine|November 22, 2023
High-Resolution and Noninvasive Fetal Exome ScreeningHarrison Brand, Christopher W Whelan, Michael Duyzend, et al.
Biorxiv : the Preprint Server for Biology|May 15, 2024
Rare germline structural variants increase risk for pediatric solid tumorsRiaz Gillani, Ryan L Collins, Jett Crowdis, et al.
Cell Stem Cell|December 18, 2014
Efficient ablation of genes in human hematopoietic stem and effector cells using CRISPR/Cas9Pankaj K Mandal, Leonardo M R Ferreira, Ryan Collins, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 1, 2026
De novo rare EMX2 variants lead to idiopathic hypogonadotropic hypogonadismMaria Stamou, Miranda Tompkins, Hannah Bow, et al.
Science (New York, N.Y.)|January 2, 2025
Rare germline structural variants increase risk for pediatric solid tumorsRiaz Gillani, Ryan L Collins, Jett Crowdis, et al.
Nature Genetics|October 13, 2020
Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathyMaria Kousi, Onuralp Söylemez, Aysegül Ozanturk, et al.
American Journal of Human Genetics|October 4, 2014
Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disordersHarrison Brand, Vamsee Pillalamarri, Ryan L Collins, et al.
Pageof 9

Showing results (11-20 of 86) with videos related to

Sort By:
Pageof 9
Proceedings of the National Academy of Sciences of the United States of America|October 9, 2014
CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitorsAarathi Sugathan, Marta Biagioli, Christelle Golzio, et al.
Nature Genetics|January 24, 2024
Author Correction: GATK-gCNV enables the discovery of rare copy number variants from exome sequencing dataMehrtash Babadi, Jack M Fu, Samuel K Lee, et al.
Nature Genetics|August 21, 2023
GATK-gCNV enables the discovery of rare copy number variants from exome sequencing dataMehrtash Babadi, Jack M Fu, Samuel K Lee, et al.
The New England Journal of Medicine|November 22, 2023
High-Resolution and Noninvasive Fetal Exome ScreeningHarrison Brand, Christopher W Whelan, Michael Duyzend, et al.
Biorxiv : the Preprint Server for Biology|May 15, 2024
Rare germline structural variants increase risk for pediatric solid tumorsRiaz Gillani, Ryan L Collins, Jett Crowdis, et al.
Cell Stem Cell|December 18, 2014
Efficient ablation of genes in human hematopoietic stem and effector cells using CRISPR/Cas9Pankaj K Mandal, Leonardo M R Ferreira, Ryan Collins, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 1, 2026
De novo rare EMX2 variants lead to idiopathic hypogonadotropic hypogonadismMaria Stamou, Miranda Tompkins, Hannah Bow, et al.
Science (New York, N.Y.)|January 2, 2025
Rare germline structural variants increase risk for pediatric solid tumorsRiaz Gillani, Ryan L Collins, Jett Crowdis, et al.
Nature Genetics|October 13, 2020
Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathyMaria Kousi, Onuralp Söylemez, Aysegül Ozanturk, et al.
American Journal of Human Genetics|October 4, 2014
Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disordersHarrison Brand, Vamsee Pillalamarri, Ryan L Collins, et al.
Pageof 9