Search research articles
Contact Us
Filters
Showing results (1-10 of 65) with videos related to
Page
of 7
Sort By:
Biorxiv : the Preprint Server for Biology
|
May 22, 2023
Insights from a genome-wide truth set of tandem repeat variation
Ben Weisburd, Grace Tiao, Heidi L Rehm
Acta Neuropathologica Communications
|
February 3, 2026
Muscle transcriptome profiling reveals novel molecular pathways and biomarkers in laminin-α2 deficient patients
Veronica Pini, Francesco Catapano, Rosa Bonaccorso, et al.
Biorxiv : the Preprint Server for Biology
|
June 6, 2025
A Tandem Repeat Atlas for the Genome of Inbred Mouse Strains: A Genetic Variation Resource
Wenlong Ren, Weida Liu, Zhuoqing Fang, et al.
Iscience
|
October 27, 2025
A tandem repeat atlas for the genome of inbred mouse strains: A genetic variation resource
Wenlong Ren, Weida Liu, Zhuoqing Fang, et al.
Wellcome Open Research
|
June 21, 2017
ClinVar data parsing
Xiaolei Zhang, Eric V Minikel, Anne H O'Donnell-Luria, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 3, 2024
STRchive: a dynamic resource detailing population-level and locus-specific insights at tandem repeat disease loci
Laurel Hiatt, Ben Weisburd, Egor Dolzhenko, et al.
Plos Pathogens
|
January 24, 2014
KSHV 2.0: a comprehensive annotation of the Kaposi's sarcoma-associated herpesvirus genome using next-generation sequencing reveals novel genomic and functional features
Carolina Arias, Ben Weisburd, Noam Stern-Ginossar, et al.
Neurology. Genetics
|
August 4, 2022
Questioning the Association of the <i>STMN2</i> Dinucleotide Repeat With Amyotrophic Lateral Sclerosis
Jay P Ross, Fulya Akçimen, Calwing Liao, et al.
Genome Medicine
|
March 27, 2025
STRchive: a dynamic resource detailing population-level and locus-specific insights at tandem repeat disease loci
Laurel Hiatt, Ben Weisburd, Egor Dolzhenko, et al.
Human Mutation
|
February 24, 2017
Pathogenic ASXL1 somatic variants in reference databases complicate germline variant interpretation for Bohring-Opitz Syndrome
Colleen M Carlston, Anne H O'Donnell-Luria, Hunter R Underhill, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 65) with videos related to
Sort By:
Page
of 7
Biorxiv : the Preprint Server for Biology
|
May 22, 2023
Insights from a genome-wide truth set of tandem repeat variation
Ben Weisburd, Grace Tiao, Heidi L Rehm
Acta Neuropathologica Communications
|
February 3, 2026
Muscle transcriptome profiling reveals novel molecular pathways and biomarkers in laminin-α2 deficient patients
Veronica Pini, Francesco Catapano, Rosa Bonaccorso, et al.
Biorxiv : the Preprint Server for Biology
|
June 6, 2025
A Tandem Repeat Atlas for the Genome of Inbred Mouse Strains: A Genetic Variation Resource
Wenlong Ren, Weida Liu, Zhuoqing Fang, et al.
Iscience
|
October 27, 2025
A tandem repeat atlas for the genome of inbred mouse strains: A genetic variation resource
Wenlong Ren, Weida Liu, Zhuoqing Fang, et al.
Wellcome Open Research
|
June 21, 2017
ClinVar data parsing
Xiaolei Zhang, Eric V Minikel, Anne H O'Donnell-Luria, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 3, 2024
STRchive: a dynamic resource detailing population-level and locus-specific insights at tandem repeat disease loci
Laurel Hiatt, Ben Weisburd, Egor Dolzhenko, et al.
Plos Pathogens
|
January 24, 2014
KSHV 2.0: a comprehensive annotation of the Kaposi's sarcoma-associated herpesvirus genome using next-generation sequencing reveals novel genomic and functional features
Carolina Arias, Ben Weisburd, Noam Stern-Ginossar, et al.
Neurology. Genetics
|
August 4, 2022
Questioning the Association of the <i>STMN2</i> Dinucleotide Repeat With Amyotrophic Lateral Sclerosis
Jay P Ross, Fulya Akçimen, Calwing Liao, et al.
Genome Medicine
|
March 27, 2025
STRchive: a dynamic resource detailing population-level and locus-specific insights at tandem repeat disease loci
Laurel Hiatt, Ben Weisburd, Egor Dolzhenko, et al.
Human Mutation
|
February 24, 2017
Pathogenic ASXL1 somatic variants in reference databases complicate germline variant interpretation for Bohring-Opitz Syndrome
Colleen M Carlston, Anne H O'Donnell-Luria, Hunter R Underhill, et al.
Page
of 7