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Medrxiv : the Preprint Server for Health Sciences
|
May 3, 2024
CWAS-Plus: Estimating category-wide association of rare noncoding variation from whole-genome sequencing data with cell-type-specific functional data
Yujin Kim, Minwoo Jeong, In Gyeong Koh, et al.
American Journal of Human Genetics
|
August 30, 2016
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families
Virpi M Leppa, Stephanie N Kravitz, Christa Lese Martin, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
December 12, 2025
Targeted BDNF upregulation via upstream open reading frame disruption
Ning Feng, Thomas Goedert, Nenad Svrzikapa, et al.
Cell Reports
|
June 8, 2024
Five autism-associated transcriptional regulators target shared loci proximal to brain-expressed genes
Siavash Fazel Darbandi, Joon-Yong An, Kenneth Lim, et al.
American Journal of Human Genetics
|
June 26, 2012
Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders
Rui Luo, Stephan J Sanders, Yuan Tian, et al.
JAMA Psychiatry
|
April 17, 2024
Examining Sex Differences in Autism Heritability
Sven Sandin, Benjamin H K Yip, Weiyao Yin, et al.
Brain & Development
|
December 20, 2011
Searching for Potocki-Lupski syndrome phenotype: a patient with language impairment and no autism
A Gulhan Ercan-Sencicek, Nicole R Davis Wright, Stephen J Frost, et al.
Plos Genetics
|
August 23, 2013
Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes
Xin He, Stephan J Sanders, Li Liu, et al.
Cell Reports
|
November 2, 2022
Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development
Winston H Cuddleston, Xuanjia Fan, Laura Sloofman, et al.
Biorxiv : the Preprint Server for Biology
|
April 10, 2023
Multiplex, single-cell CRISPRa screening for cell type specific regulatory elements
Florence M Chardon, Troy A McDiarmid, Nicholas F Page, et al.
Page
of 16
Search research articles
Search
Showing results (41-50 of 154) with videos related to
Sort By:
Page
of 16
Medrxiv : the Preprint Server for Health Sciences
|
May 3, 2024
CWAS-Plus: Estimating category-wide association of rare noncoding variation from whole-genome sequencing data with cell-type-specific functional data
Yujin Kim, Minwoo Jeong, In Gyeong Koh, et al.
American Journal of Human Genetics
|
August 30, 2016
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families
Virpi M Leppa, Stephanie N Kravitz, Christa Lese Martin, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
December 12, 2025
Targeted BDNF upregulation via upstream open reading frame disruption
Ning Feng, Thomas Goedert, Nenad Svrzikapa, et al.
Cell Reports
|
June 8, 2024
Five autism-associated transcriptional regulators target shared loci proximal to brain-expressed genes
Siavash Fazel Darbandi, Joon-Yong An, Kenneth Lim, et al.
American Journal of Human Genetics
|
June 26, 2012
Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders
Rui Luo, Stephan J Sanders, Yuan Tian, et al.
JAMA Psychiatry
|
April 17, 2024
Examining Sex Differences in Autism Heritability
Sven Sandin, Benjamin H K Yip, Weiyao Yin, et al.
Brain & Development
|
December 20, 2011
Searching for Potocki-Lupski syndrome phenotype: a patient with language impairment and no autism
A Gulhan Ercan-Sencicek, Nicole R Davis Wright, Stephen J Frost, et al.
Plos Genetics
|
August 23, 2013
Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes
Xin He, Stephan J Sanders, Li Liu, et al.
Cell Reports
|
November 2, 2022
Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development
Winston H Cuddleston, Xuanjia Fan, Laura Sloofman, et al.
Biorxiv : the Preprint Server for Biology
|
April 10, 2023
Multiplex, single-cell CRISPRa screening for cell type specific regulatory elements
Florence M Chardon, Troy A McDiarmid, Nicholas F Page, et al.
Page
of 16