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European Journal of Human Genetics : EJHG
|
April 9, 2025
Benchmark of computational methods to detect digenism in sequencing data
Marie-Sophie C Ogloblinsky, Donald F Conrad, Anaïs Baudot, et al.
Elife
|
June 26, 2019
Unified single-cell analysis of testis gene regulation and pathology in five mouse strains
Min Jung, Daniel Wells, Jannette Rusch, et al.
BMC Genomics
|
May 29, 2015
Using whole-genome sequences of the LG/J and SM/J inbred mouse strains to prioritize quantitative trait genes and nucleotides
Igor Nikolskiy, Donald F Conrad, Sung Chun, et al.
Genome Research
|
November 20, 2023
A naturally occurring variant of <i>MBD4</i> causes maternal germline hypermutation in primates
Alexandra M Stendahl, Rashesh Sanghvi, Samuel Peterson, et al.
Bioinformatics (Oxford, England)
|
October 10, 2022
SATINN: an automated neural network-based classification of testicular sections allows for high-throughput histopathology of mouse mutants
Ran Yang, Alexandra M Stendahl, Katinka A Vigh-Conrad, et al.
Human Molecular Genetics
|
April 2, 2009
Inverted duplications on acentric markers: mechanism of formation
Andrea E Murmann, Donald F Conrad, Heather Mashek, et al.
Nature Genetics
|
November 8, 2016
Genome-wide significance testing of variation from single case exomes
Amy B Wilfert, Katherine R Chao, Madhurima Kaushal, et al.
Digestive Diseases and Sciences
|
March 27, 2002
Validation of Spanish language dyspepsia questionnaire
Jonathan Goldman, Donald F Conrad, Catherine Ley, et al.
Nature Genetics
|
October 24, 2006
A worldwide survey of haplotype variation and linkage disequilibrium in the human genome
Donald F Conrad, Mattias Jakobsson, Graham Coop, et al.
Nature Genetics
|
April 6, 2010
Mutation spectrum revealed by breakpoint sequencing of human germline CNVs
Donald F Conrad, Christine Bird, Ben Blackburne, et al.
Page
of 11
Search research articles
Search
Showing results (21-30 of 106) with videos related to
Sort By:
Page
of 11
European Journal of Human Genetics : EJHG
|
April 9, 2025
Benchmark of computational methods to detect digenism in sequencing data
Marie-Sophie C Ogloblinsky, Donald F Conrad, Anaïs Baudot, et al.
Elife
|
June 26, 2019
Unified single-cell analysis of testis gene regulation and pathology in five mouse strains
Min Jung, Daniel Wells, Jannette Rusch, et al.
BMC Genomics
|
May 29, 2015
Using whole-genome sequences of the LG/J and SM/J inbred mouse strains to prioritize quantitative trait genes and nucleotides
Igor Nikolskiy, Donald F Conrad, Sung Chun, et al.
Genome Research
|
November 20, 2023
A naturally occurring variant of <i>MBD4</i> causes maternal germline hypermutation in primates
Alexandra M Stendahl, Rashesh Sanghvi, Samuel Peterson, et al.
Bioinformatics (Oxford, England)
|
October 10, 2022
SATINN: an automated neural network-based classification of testicular sections allows for high-throughput histopathology of mouse mutants
Ran Yang, Alexandra M Stendahl, Katinka A Vigh-Conrad, et al.
Human Molecular Genetics
|
April 2, 2009
Inverted duplications on acentric markers: mechanism of formation
Andrea E Murmann, Donald F Conrad, Heather Mashek, et al.
Nature Genetics
|
November 8, 2016
Genome-wide significance testing of variation from single case exomes
Amy B Wilfert, Katherine R Chao, Madhurima Kaushal, et al.
Digestive Diseases and Sciences
|
March 27, 2002
Validation of Spanish language dyspepsia questionnaire
Jonathan Goldman, Donald F Conrad, Catherine Ley, et al.
Nature Genetics
|
October 24, 2006
A worldwide survey of haplotype variation and linkage disequilibrium in the human genome
Donald F Conrad, Mattias Jakobsson, Graham Coop, et al.
Nature Genetics
|
April 6, 2010
Mutation spectrum revealed by breakpoint sequencing of human germline CNVs
Donald F Conrad, Christine Bird, Ben Blackburne, et al.
Page
of 11