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BMC Neuroscience
|
July 9, 2016
Characterization of a novel zebrafish (Danio rerio) gene, wdr81, associated with cerebellar ataxia, mental retardation and dysequilibrium syndrome (CAMRQ)
Fusun Doldur-Balli, Mehmet Neset Ozel, Suleyman Gulsuner, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 2, 2018
De novo mutation in <i>RING1</i> with epigenetic effects on neurodevelopment
Sarah B Pierce, Mikaela D Stewart, Suleyman Gulsuner, et al.
European Journal of Human Genetics : EJHG
|
August 16, 2012
Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion
Onur Emre Onat, Suleyman Gulsuner, Kaya Bilguvar, et al.
Plos One
|
September 30, 2020
Effects of germline and somatic events in candidate BRCA-like genes on breast-tumor signatures
Weston R Bodily, Brian H Shirts, Tom Walsh, et al.
NPJ Breast Cancer
|
January 22, 2021
Inherited predisposition to breast cancer in the Carolina Breast Cancer Study
Tom Walsh, Suleyman Gulsuner, Ming K Lee, et al.
Genome Research
|
September 13, 2024
Long-read DNA and cDNA sequencing identify cancer-predisposing deep intronic variation in tumor-suppressor genes
Suleyman Gulsuner, Amal AbuRayyan, Jessica B Mandell, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 21, 2020
NKX2-2 Mutation Causes Congenital Diabetes and Infantile Obesity With Paradoxical Glucose-Induced Ghrelin Secretion
Adi Auerbach, Amitay Cohen, Noa Ofek Shlomai, et al.
Human Molecular Genetics
|
April 19, 2023
A paradoxical genotype-phenotype relationship: Low level of GOSR2 translation from a non-AUG start codon in a family with profound hearing loss
Amal Aburayyan, Ryan J Carlson, Grace N Rabie, et al.
Human Molecular Genetics
|
September 25, 2018
Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE)
Aaron Seo, Suleyman Gulsuner, Sarah Pierce, et al.
Haematologica
|
July 16, 2016
Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients
Siobán B Keel, Angela Scott, Marilyn Sanchez-Bonilla, et al.
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of 7
Search research articles
Search
Showing results (11-20 of 63) with videos related to
Sort By:
Page
of 7
BMC Neuroscience
|
July 9, 2016
Characterization of a novel zebrafish (Danio rerio) gene, wdr81, associated with cerebellar ataxia, mental retardation and dysequilibrium syndrome (CAMRQ)
Fusun Doldur-Balli, Mehmet Neset Ozel, Suleyman Gulsuner, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 2, 2018
De novo mutation in <i>RING1</i> with epigenetic effects on neurodevelopment
Sarah B Pierce, Mikaela D Stewart, Suleyman Gulsuner, et al.
European Journal of Human Genetics : EJHG
|
August 16, 2012
Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion
Onur Emre Onat, Suleyman Gulsuner, Kaya Bilguvar, et al.
Plos One
|
September 30, 2020
Effects of germline and somatic events in candidate BRCA-like genes on breast-tumor signatures
Weston R Bodily, Brian H Shirts, Tom Walsh, et al.
NPJ Breast Cancer
|
January 22, 2021
Inherited predisposition to breast cancer in the Carolina Breast Cancer Study
Tom Walsh, Suleyman Gulsuner, Ming K Lee, et al.
Genome Research
|
September 13, 2024
Long-read DNA and cDNA sequencing identify cancer-predisposing deep intronic variation in tumor-suppressor genes
Suleyman Gulsuner, Amal AbuRayyan, Jessica B Mandell, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 21, 2020
NKX2-2 Mutation Causes Congenital Diabetes and Infantile Obesity With Paradoxical Glucose-Induced Ghrelin Secretion
Adi Auerbach, Amitay Cohen, Noa Ofek Shlomai, et al.
Human Molecular Genetics
|
April 19, 2023
A paradoxical genotype-phenotype relationship: Low level of GOSR2 translation from a non-AUG start codon in a family with profound hearing loss
Amal Aburayyan, Ryan J Carlson, Grace N Rabie, et al.
Human Molecular Genetics
|
September 25, 2018
Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE)
Aaron Seo, Suleyman Gulsuner, Sarah Pierce, et al.
Haematologica
|
July 16, 2016
Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients
Siobán B Keel, Angela Scott, Marilyn Sanchez-Bonilla, et al.
Page
of 7