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American Journal of Human Genetics
|
October 4, 2024
Joint testing of rare variant burden scores using non-negative least squares
Andrey Ziyatdinov, Joelle Mbatchou, Anthony Marcketta, et al.
Human Molecular Genetics
|
April 11, 2018
MIR137 schizophrenia-associated locus controls synaptic function by regulating synaptogenesis, synapse maturation and synaptic transmission
Enqi He, Miguel A Gonzalez Lozano, Sven Stringer, et al.
Pediatric Neurology
|
January 18, 2017
Clinical Epidemiology and Treatment of Febrile and Afebrile Convulsions With Mild Gastroenteritis: A Multicenter Study
Yousuke Higuchi, Toshihide Kubo, Toshiharu Mitsuhashi, et al.
Cell Reports
|
July 6, 2022
Molecular signatures and cellular diversity during mouse habenula development
Lieke L van de Haar, Danai Riga, Juliska E Boer, et al.
Diabetes Therapy : Research, Treatment and Education of Diabetes and Related Disorders
|
March 21, 2022
Additional Effect of Luseogliflozin on Semaglutide in Nonalcoholic Steatohepatitis Complicated by Type 2 Diabetes Mellitus: An Open-Label, Randomized, Parallel-Group Study
Teruki Miyake, Osamu Yoshida, Bunzo Matsuura, et al.
Journal of Human Genetics
|
August 19, 2011
HRAS mutants identified in Costello syndrome patients can induce cellular senescence: possible implications for the pathogenesis of Costello syndrome
Tetsuya Niihori, Yoko Aoki, Nobuhiko Okamoto, et al.
Nature Genetics
|
June 27, 2018
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways
Mats Nagel, Philip R Jansen, Sven Stringer, et al.
The Journal of Clinical Investigation
|
October 3, 2023
A splice-switching oligonucleotide treatment ameliorates glycogen storage disease type 1a in mice with G6PC c.648G>T
Kentaro Ito, Go Tajima, Chikako Kamisato, et al.
Nature Genetics
|
June 13, 2017
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits
Anke R Hammerschlag, Sven Stringer, Christiaan A de Leeuw, et al.
Brain & Development
|
August 31, 2014
Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications
Shino Shimada, Keiko Shimojima, Nobuhiko Okamoto, et al.
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Search research articles
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Showing results (71-80 of 99) with videos related to
Sort By:
Page
of 10
American Journal of Human Genetics
|
October 4, 2024
Joint testing of rare variant burden scores using non-negative least squares
Andrey Ziyatdinov, Joelle Mbatchou, Anthony Marcketta, et al.
Human Molecular Genetics
|
April 11, 2018
MIR137 schizophrenia-associated locus controls synaptic function by regulating synaptogenesis, synapse maturation and synaptic transmission
Enqi He, Miguel A Gonzalez Lozano, Sven Stringer, et al.
Pediatric Neurology
|
January 18, 2017
Clinical Epidemiology and Treatment of Febrile and Afebrile Convulsions With Mild Gastroenteritis: A Multicenter Study
Yousuke Higuchi, Toshihide Kubo, Toshiharu Mitsuhashi, et al.
Cell Reports
|
July 6, 2022
Molecular signatures and cellular diversity during mouse habenula development
Lieke L van de Haar, Danai Riga, Juliska E Boer, et al.
Diabetes Therapy : Research, Treatment and Education of Diabetes and Related Disorders
|
March 21, 2022
Additional Effect of Luseogliflozin on Semaglutide in Nonalcoholic Steatohepatitis Complicated by Type 2 Diabetes Mellitus: An Open-Label, Randomized, Parallel-Group Study
Teruki Miyake, Osamu Yoshida, Bunzo Matsuura, et al.
Journal of Human Genetics
|
August 19, 2011
HRAS mutants identified in Costello syndrome patients can induce cellular senescence: possible implications for the pathogenesis of Costello syndrome
Tetsuya Niihori, Yoko Aoki, Nobuhiko Okamoto, et al.
Nature Genetics
|
June 27, 2018
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways
Mats Nagel, Philip R Jansen, Sven Stringer, et al.
The Journal of Clinical Investigation
|
October 3, 2023
A splice-switching oligonucleotide treatment ameliorates glycogen storage disease type 1a in mice with G6PC c.648G>T
Kentaro Ito, Go Tajima, Chikako Kamisato, et al.
Nature Genetics
|
June 13, 2017
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits
Anke R Hammerschlag, Sven Stringer, Christiaan A de Leeuw, et al.
Brain & Development
|
August 31, 2014
Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications
Shino Shimada, Keiko Shimojima, Nobuhiko Okamoto, et al.
Page
of 10