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Journal of Clinical Medicine
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December 17, 2024
Screening for Hypophosphatasia in Adult Patients at a Maximum Care Provider-Retrospective Analyses over Fifteen Years
Robert Hennings, Diana Le Duc, Linnaeus Bundalian, et al.
Liver International : Official Journal of the International Association for the Study of the Liver
|
May 4, 2024
Thy-1 restricts steatosis and liver fibrosis in steatotic liver disease
Valentin Blank, Thomas Karlas, Ulf Anderegg, et al.
Biomolecules
|
October 23, 2021
Obesity-An Update on the Basic Pathophysiology and Review of Recent Therapeutic Advances
Erind Gjermeni, Anna S Kirstein, Florentien Kolbig, et al.
Journal of Neurogenetics
|
February 25, 2025
<i>Drosophila WDFY3</i>/<i>Bchs</i> overexpression impairs neural function
Marek B Körner, Akhil Velluva, Linnaeus Bundalian, et al.
American Journal of Human Genetics
|
June 27, 2023
Epilepsies of presumed genetic etiology show enrichment of rare variants that occur in the general population
Linnaeus Bundalian, Yin-Yuan Su, Siwei Chen, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 28, 2023
The role of rare genetic variants enrichment in epilepsies of presumed genetic etiology
Linnaeus Bundalian, Yin-Yuan Su, Siwei Chen, et al.
International Journal of Obesity (2005)
|
June 16, 2025
Detecting monogenic obesity: a systematic exome-wide workup of over 500 individuals
Robert Künzel, Helene Faust, Linnaeus Bundalian, et al.
NAR Genomics and Bioinformatics
|
January 19, 2026
SyMetrics: an integrated machine learning model for evaluating the pathogenicity of synonymous variants in the human genome
Linnaeus Bundalian, Martina Schmidt Strnadová, Felix Garten, et al.
Brain : a Journal of Neurology
|
March 15, 2024
Dominant CST3 variants cause adult onset leukodystrophy without amyloid angiopathy
Caroline G Bergner, Marjolein Breur, M Clara Soto-Bernardini, et al.
Scientific Reports
|
August 5, 2022
Altered gene expression profiles impair the nervous system development in individuals with 15q13.3 microdeletion
Marek B Körner, Akhil Velluva, Linnaeus Bundalian, et al.
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of 1
Search research articles
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Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Journal of Clinical Medicine
|
December 17, 2024
Screening for Hypophosphatasia in Adult Patients at a Maximum Care Provider-Retrospective Analyses over Fifteen Years
Robert Hennings, Diana Le Duc, Linnaeus Bundalian, et al.
Liver International : Official Journal of the International Association for the Study of the Liver
|
May 4, 2024
Thy-1 restricts steatosis and liver fibrosis in steatotic liver disease
Valentin Blank, Thomas Karlas, Ulf Anderegg, et al.
Biomolecules
|
October 23, 2021
Obesity-An Update on the Basic Pathophysiology and Review of Recent Therapeutic Advances
Erind Gjermeni, Anna S Kirstein, Florentien Kolbig, et al.
Journal of Neurogenetics
|
February 25, 2025
<i>Drosophila WDFY3</i>/<i>Bchs</i> overexpression impairs neural function
Marek B Körner, Akhil Velluva, Linnaeus Bundalian, et al.
American Journal of Human Genetics
|
June 27, 2023
Epilepsies of presumed genetic etiology show enrichment of rare variants that occur in the general population
Linnaeus Bundalian, Yin-Yuan Su, Siwei Chen, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 28, 2023
The role of rare genetic variants enrichment in epilepsies of presumed genetic etiology
Linnaeus Bundalian, Yin-Yuan Su, Siwei Chen, et al.
International Journal of Obesity (2005)
|
June 16, 2025
Detecting monogenic obesity: a systematic exome-wide workup of over 500 individuals
Robert Künzel, Helene Faust, Linnaeus Bundalian, et al.
NAR Genomics and Bioinformatics
|
January 19, 2026
SyMetrics: an integrated machine learning model for evaluating the pathogenicity of synonymous variants in the human genome
Linnaeus Bundalian, Martina Schmidt Strnadová, Felix Garten, et al.
Brain : a Journal of Neurology
|
March 15, 2024
Dominant CST3 variants cause adult onset leukodystrophy without amyloid angiopathy
Caroline G Bergner, Marjolein Breur, M Clara Soto-Bernardini, et al.
Scientific Reports
|
August 5, 2022
Altered gene expression profiles impair the nervous system development in individuals with 15q13.3 microdeletion
Marek B Körner, Akhil Velluva, Linnaeus Bundalian, et al.
Page
of 1