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Nature
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September 18, 2009
Genetic variation in IL28B and spontaneous clearance of hepatitis C virus
David L Thomas, Chloe L Thio, Maureen P Martin, et al.
American Journal of Respiratory and Critical Care Medicine
|
April 13, 2022
Rare and Common Variants in <i>KIF15</i> Contribute to Genetic Risk of Idiopathic Pulmonary Fibrosis
David Zhang, Gundula Povysil, Philippe H Kobeissy, et al.
American Journal of Human Genetics
|
August 7, 2012
Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia
Anna C Need, Joseph P McEvoy, Massimo Gennarelli, et al.
Digestive Diseases and Sciences
|
May 1, 2012
The association of genetic variants with hepatic steatosis in patients with genotype 1 chronic hepatitis C infection
Paul J Clark, Alexander J Thompson, Qianqian Zhu, et al.
Scientific Reports
|
December 6, 2023
The diagnostic yield of exome sequencing in liver diseases from a curated gene panel
Xiao-Fei Kong, Kelsie Bogyo, Sheena Kapoor, et al.
American Journal of Human Genetics
|
July 26, 2016
Mutations of the Sonic Hedgehog Pathway Underlie Hypothalamic Hamartoma with Gelastic Epilepsy
Michael S Hildebrand, Nicole G Griffin, John A Damiano, et al.
Plos Biology
|
December 6, 2011
Copy number variation of KIR genes influences HIV-1 control
Kimberly Pelak, Anna C Need, Jacques Fellay, et al.
Pharmacogenetics and Genomics
|
September 13, 2012
Limited contribution of common genetic variants to risk for liver injury due to a variety of drugs
Thomas J Urban, Yufeng Shen, Andrew Stolz, et al.
Molecular Psychiatry
|
November 20, 2021
The benefit of diagnostic whole genome sequencing in schizophrenia and other psychotic disorders
Anna Alkelai, Lior Greenbaum, Anna R Docherty, et al.
Seizure
|
November 5, 2013
Gaps and opportunities in refractory status epilepticus research in children: a multi-center approach by the Pediatric Status Epilepticus Research Group (pSERG)
Iván Sánchez Fernández, Nicholas S Abend, Satish Agadi, et al.
Page
of 34
Search research articles
Search
Showing results (251-260 of 338) with videos related to
Sort By:
Page
of 34
Nature
|
September 18, 2009
Genetic variation in IL28B and spontaneous clearance of hepatitis C virus
David L Thomas, Chloe L Thio, Maureen P Martin, et al.
American Journal of Respiratory and Critical Care Medicine
|
April 13, 2022
Rare and Common Variants in <i>KIF15</i> Contribute to Genetic Risk of Idiopathic Pulmonary Fibrosis
David Zhang, Gundula Povysil, Philippe H Kobeissy, et al.
American Journal of Human Genetics
|
August 7, 2012
Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia
Anna C Need, Joseph P McEvoy, Massimo Gennarelli, et al.
Digestive Diseases and Sciences
|
May 1, 2012
The association of genetic variants with hepatic steatosis in patients with genotype 1 chronic hepatitis C infection
Paul J Clark, Alexander J Thompson, Qianqian Zhu, et al.
Scientific Reports
|
December 6, 2023
The diagnostic yield of exome sequencing in liver diseases from a curated gene panel
Xiao-Fei Kong, Kelsie Bogyo, Sheena Kapoor, et al.
American Journal of Human Genetics
|
July 26, 2016
Mutations of the Sonic Hedgehog Pathway Underlie Hypothalamic Hamartoma with Gelastic Epilepsy
Michael S Hildebrand, Nicole G Griffin, John A Damiano, et al.
Plos Biology
|
December 6, 2011
Copy number variation of KIR genes influences HIV-1 control
Kimberly Pelak, Anna C Need, Jacques Fellay, et al.
Pharmacogenetics and Genomics
|
September 13, 2012
Limited contribution of common genetic variants to risk for liver injury due to a variety of drugs
Thomas J Urban, Yufeng Shen, Andrew Stolz, et al.
Molecular Psychiatry
|
November 20, 2021
The benefit of diagnostic whole genome sequencing in schizophrenia and other psychotic disorders
Anna Alkelai, Lior Greenbaum, Anna R Docherty, et al.
Seizure
|
November 5, 2013
Gaps and opportunities in refractory status epilepticus research in children: a multi-center approach by the Pediatric Status Epilepticus Research Group (pSERG)
Iván Sánchez Fernández, Nicholas S Abend, Satish Agadi, et al.
Page
of 34