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Susan Walker

Showing results (231-240 of 260) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Blood-based RNA-Seq of 5412 individuals with rare disease identifies new candidate diagnoses in the National Genomic Research LibraryJenny Lord, Alistair T Pagnamenta, Letizia Vestito, et al.
JAMA|September 2, 2015
Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum DisorderKristiina Tammimies, Christian R Marshall, Susan Walker, et al.
Human Molecular Genetics|May 27, 2025
KDM2B variants in the CxxC domain impair its DNA-binding ability and cause a distinct neurodevelopmental syndromeAmber S E van Oirsouw, Michael A Hadders, Martijn Koetsier, et al.
American Journal of Human Genetics|July 16, 2013
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencingYong-hui Jiang, Ryan K C Yuen, Xin Jin, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 31, 2024
Large-Scale Pharmacogenomics Analysis of Patients With Cancer Within the 100,000 Genomes Project Combining Whole-Genome Sequencing and Medical Records to Inform Clinical PracticeIvone U S Leong, Claudia P Cabrera, Valentina Cipriani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 22, 2023
Secondary (additional) findings from the 100,000 Genomes Project: Disease manifestation, health care outcomes, and costs of disclosureJoshua Nolan, James Buchanan, John Taylor, et al.
G3 (Bethesda, Md.)|January 15, 2017
<i>De Novo</i> Genome and Transcriptome Assembly of the Canadian Beaver (<i>Castor canadensis</i>)Si Lok, Tara A Paton, Zhuozhi Wang, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2025
Single-cell immune profiling of third trimester pregnancies defines importance of chemokine receptors and prevalence of CMV-induced NK cells in the periphery and deciduaJennifer R Habel, Thi H O Nguyen, Lilith F Allen, et al.
Frontiers in Public Health|February 13, 2026
Replanting the Birthing Trees to support Aboriginal and Torres Strait Islander parents and babies: protocol for developmental evaluation of a comprehensive culturally responsive, trauma-aware, healing-informed, continuity of care(r) modelCatherine Chamberlain, Jacqui Sundbery, Leonie Segal, et al.
NPJ Genomic Medicine|August 16, 2016
Genome-wide characteristics of <i>de novo</i> mutations in autismRyan K C Yuen, Daniele Merico, Hongzhi Cao, et al.
Pageof 26

Showing results (231-240 of 260) with videos related to

Sort By:
Pageof 26
Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Blood-based RNA-Seq of 5412 individuals with rare disease identifies new candidate diagnoses in the National Genomic Research LibraryJenny Lord, Alistair T Pagnamenta, Letizia Vestito, et al.
JAMA|September 2, 2015
Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum DisorderKristiina Tammimies, Christian R Marshall, Susan Walker, et al.
Human Molecular Genetics|May 27, 2025
KDM2B variants in the CxxC domain impair its DNA-binding ability and cause a distinct neurodevelopmental syndromeAmber S E van Oirsouw, Michael A Hadders, Martijn Koetsier, et al.
American Journal of Human Genetics|July 16, 2013
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencingYong-hui Jiang, Ryan K C Yuen, Xin Jin, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 31, 2024
Large-Scale Pharmacogenomics Analysis of Patients With Cancer Within the 100,000 Genomes Project Combining Whole-Genome Sequencing and Medical Records to Inform Clinical PracticeIvone U S Leong, Claudia P Cabrera, Valentina Cipriani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 22, 2023
Secondary (additional) findings from the 100,000 Genomes Project: Disease manifestation, health care outcomes, and costs of disclosureJoshua Nolan, James Buchanan, John Taylor, et al.
G3 (Bethesda, Md.)|January 15, 2017
<i>De Novo</i> Genome and Transcriptome Assembly of the Canadian Beaver (<i>Castor canadensis</i>)Si Lok, Tara A Paton, Zhuozhi Wang, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2025
Single-cell immune profiling of third trimester pregnancies defines importance of chemokine receptors and prevalence of CMV-induced NK cells in the periphery and deciduaJennifer R Habel, Thi H O Nguyen, Lilith F Allen, et al.
Frontiers in Public Health|February 13, 2026
Replanting the Birthing Trees to support Aboriginal and Torres Strait Islander parents and babies: protocol for developmental evaluation of a comprehensive culturally responsive, trauma-aware, healing-informed, continuity of care(r) modelCatherine Chamberlain, Jacqui Sundbery, Leonie Segal, et al.
NPJ Genomic Medicine|August 16, 2016
Genome-wide characteristics of <i>de novo</i> mutations in autismRyan K C Yuen, Daniele Merico, Hongzhi Cao, et al.
Pageof 26