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Bone
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November 28, 2017
Gnathodiaphyseal dysplasia: Severe atypical presentation with novel heterozygous mutation of the anoctamin gene (ANO5)
Ghada A Otaify, Michael P Whyte, Gary S Gottesman, et al.
Genome Medicine
|
March 29, 2018
Elevated polygenic burden for autism is associated with differential DNA methylation at birth
Eilis Hannon, Diana Schendel, Christine Ladd-Acosta, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 9, 2021
Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain
Felix Marbach, Georgi Stoyanov, Florian Erger, et al.
Communications Biology
|
August 16, 2023
Global endometrial DNA methylation analysis reveals insights into mQTL regulation and associated endometriosis disease risk and endometrial function
Sally Mortlock, Sahar Houshdaran, Idit Kosti, et al.
Journal of Environmental Management
|
October 30, 2024
Using systems mapping to understand the constraints and enablers of solutions to plastic pollution
E K Morasae, Z L R Botterell, S H V Andrews, et al.
Genome Medicine
|
August 16, 2017
Phenotypic and molecular characterisation of CDK13-related congenital heart defects, dysmorphic facial features and intellectual developmental disorders
Bret L Bostwick, Scott McLean, Jennifer E Posey, et al.
Molecular Neurodegeneration
|
August 7, 2025
LRRK2 kinase activity regulates Parkinson's disease-relevant lipids at the lysosome
Michael T Maloney, Xiang Wang, Rajarshi Ghosh, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 28, 2023
The Genetic Drivers of Juvenile, Young, and Early-Onset Parkinson's Disease in India
Shan V Andrews, Prashanth L Kukkle, Ramesh Menon, et al.
Biorxiv : the Preprint Server for Biology
|
October 1, 2025
A Common PD-Risk <i>GBA1</i> Variant Disrupts LIMP2 Interaction, Impairs Glucocerebrosidase Function, and Drives Lysosomal and Mitochondrial Dysfunction
Oliver B Davis, Jennifer E Kung, Sonnet S Davis, et al.
Cancer Research
|
May 13, 2020
A Custom Genotyping Array Reveals Population-Level Heterogeneity for the Genetic Risks of Prostate Cancer and Other Cancers in Africa
Maxine Harlemon, Olabode Ajayi, Paidamoyo Kachambwa, et al.
Page
of 16
Search research articles
Search
Showing results (141-150 of 157) with videos related to
Sort By:
Page
of 16
Bone
|
November 28, 2017
Gnathodiaphyseal dysplasia: Severe atypical presentation with novel heterozygous mutation of the anoctamin gene (ANO5)
Ghada A Otaify, Michael P Whyte, Gary S Gottesman, et al.
Genome Medicine
|
March 29, 2018
Elevated polygenic burden for autism is associated with differential DNA methylation at birth
Eilis Hannon, Diana Schendel, Christine Ladd-Acosta, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 9, 2021
Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain
Felix Marbach, Georgi Stoyanov, Florian Erger, et al.
Communications Biology
|
August 16, 2023
Global endometrial DNA methylation analysis reveals insights into mQTL regulation and associated endometriosis disease risk and endometrial function
Sally Mortlock, Sahar Houshdaran, Idit Kosti, et al.
Journal of Environmental Management
|
October 30, 2024
Using systems mapping to understand the constraints and enablers of solutions to plastic pollution
E K Morasae, Z L R Botterell, S H V Andrews, et al.
Genome Medicine
|
August 16, 2017
Phenotypic and molecular characterisation of CDK13-related congenital heart defects, dysmorphic facial features and intellectual developmental disorders
Bret L Bostwick, Scott McLean, Jennifer E Posey, et al.
Molecular Neurodegeneration
|
August 7, 2025
LRRK2 kinase activity regulates Parkinson's disease-relevant lipids at the lysosome
Michael T Maloney, Xiang Wang, Rajarshi Ghosh, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 28, 2023
The Genetic Drivers of Juvenile, Young, and Early-Onset Parkinson's Disease in India
Shan V Andrews, Prashanth L Kukkle, Ramesh Menon, et al.
Biorxiv : the Preprint Server for Biology
|
October 1, 2025
A Common PD-Risk <i>GBA1</i> Variant Disrupts LIMP2 Interaction, Impairs Glucocerebrosidase Function, and Drives Lysosomal and Mitochondrial Dysfunction
Oliver B Davis, Jennifer E Kung, Sonnet S Davis, et al.
Cancer Research
|
May 13, 2020
A Custom Genotyping Array Reveals Population-Level Heterogeneity for the Genetic Risks of Prostate Cancer and Other Cancers in Africa
Maxine Harlemon, Olabode Ajayi, Paidamoyo Kachambwa, et al.
Page
of 16