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Metabolism: Clinical and Experimental
|
December 14, 2020
Serum uric acid is associated with increased risk of posttransplantation diabetes in kidney transplant recipients: a prospective cohort study
Camilo G Sotomayor, Sara Sokooti Oskooei, Nicolás I Bustos, et al.
Human Molecular Genetics
|
July 2, 2004
Single nucleotide polymorphisms in protein tyrosine phosphatase 1beta (PTPN1) are associated with essential hypertension and obesity
Michael Olivier, Chao A Hsiung, Lee-Ming Chuang, et al.
Neurobiology of Aging
|
December 11, 2012
A novel functional low-density lipoprotein receptor-related protein 6 gene alternative splice variant is associated with Alzheimer's disease
Marcelo A Alarcón, Matías A Medina, Qubai Hu, et al.
Elife
|
February 5, 2021
Dyshomeostatic modulation of Ca<sup>2+</sup>-activated K<sup>+</sup> channels in a human neuronal model of KCNQ2 encephalopathy
Dina Simkin, Kelly A Marshall, Carlos G Vanoye, et al.
Genomics
|
November 15, 2001
Complex high-resolution linkage disequilibrium and haplotype patterns of single-nucleotide polymorphisms in 2.5 Mb of sequence on human chromosome 21
M Olivier, V I Bustos, M R Levy, et al.
Brain : a Journal of Neurology
|
March 2, 2023
Variants in ATP5F1B are associated with dominantly inherited dystonia
Alessia Nasca, Niccolò E Mencacci, Federica Invernizzi, et al.
European Journal of Human Genetics : EJHG
|
September 6, 2019
Copy number variants in lipid metabolism genes are associated with gallstones disease in men
Eduardo Pérez-Palma, Bernabé I Bustos, Dennis Lal, et al.
Scientific Reports
|
January 30, 2019
Variants in ABCG8 and TRAF3 genes confer risk for gallstone disease in admixed Latinos with Mapuche Native American ancestry
Bernabé I Bustos, Eduardo Pérez-Palma, Stephan Buch, et al.
Brain : a Journal of Neurology
|
May 26, 2026
Is SORL1 a common genetic target across neurodegenerative diseases? A multi-ancestry biobank study
Marzieh Khani, Sheila N Yeboah, Catalina Cerquera-Cleves, et al.
Scientific Reports
|
February 16, 2019
Whole Genome Sequence, Variant Discovery and Annotation in Mapuche-Huilliche Native South Americans
Elena A Vidal, Tomás C Moyano, Bernabé I Bustos, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 45) with videos related to
Sort By:
Page
of 5
Metabolism: Clinical and Experimental
|
December 14, 2020
Serum uric acid is associated with increased risk of posttransplantation diabetes in kidney transplant recipients: a prospective cohort study
Camilo G Sotomayor, Sara Sokooti Oskooei, Nicolás I Bustos, et al.
Human Molecular Genetics
|
July 2, 2004
Single nucleotide polymorphisms in protein tyrosine phosphatase 1beta (PTPN1) are associated with essential hypertension and obesity
Michael Olivier, Chao A Hsiung, Lee-Ming Chuang, et al.
Neurobiology of Aging
|
December 11, 2012
A novel functional low-density lipoprotein receptor-related protein 6 gene alternative splice variant is associated with Alzheimer's disease
Marcelo A Alarcón, Matías A Medina, Qubai Hu, et al.
Elife
|
February 5, 2021
Dyshomeostatic modulation of Ca<sup>2+</sup>-activated K<sup>+</sup> channels in a human neuronal model of KCNQ2 encephalopathy
Dina Simkin, Kelly A Marshall, Carlos G Vanoye, et al.
Genomics
|
November 15, 2001
Complex high-resolution linkage disequilibrium and haplotype patterns of single-nucleotide polymorphisms in 2.5 Mb of sequence on human chromosome 21
M Olivier, V I Bustos, M R Levy, et al.
Brain : a Journal of Neurology
|
March 2, 2023
Variants in ATP5F1B are associated with dominantly inherited dystonia
Alessia Nasca, Niccolò E Mencacci, Federica Invernizzi, et al.
European Journal of Human Genetics : EJHG
|
September 6, 2019
Copy number variants in lipid metabolism genes are associated with gallstones disease in men
Eduardo Pérez-Palma, Bernabé I Bustos, Dennis Lal, et al.
Scientific Reports
|
January 30, 2019
Variants in ABCG8 and TRAF3 genes confer risk for gallstone disease in admixed Latinos with Mapuche Native American ancestry
Bernabé I Bustos, Eduardo Pérez-Palma, Stephan Buch, et al.
Brain : a Journal of Neurology
|
May 26, 2026
Is SORL1 a common genetic target across neurodegenerative diseases? A multi-ancestry biobank study
Marzieh Khani, Sheila N Yeboah, Catalina Cerquera-Cleves, et al.
Scientific Reports
|
February 16, 2019
Whole Genome Sequence, Variant Discovery and Annotation in Mapuche-Huilliche Native South Americans
Elena A Vidal, Tomás C Moyano, Bernabé I Bustos, et al.
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of 5