Search research articles
Contact Us
Filters
Showing results (191-200 of 205) with videos related to
Page
of 21
Sort By:
European Journal of Human Genetics : EJHG
|
September 12, 2013
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
Jessica Becker, Darina Czamara, Tom S Scerri, et al.
American Journal of Human Genetics
|
December 1, 2014
Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndrome
Dagmar Wieczorek, William G Newman, Thomas Wieland, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 11, 2016
Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis
Charlotte W Ockeloen, Kriti D Khandelwal, Karoline Dreesen, et al.
The Journal of Clinical Investigation
|
October 1, 2021
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality
Tomoko Nakanishi, Sara Pigazzini, Frauke Degenhardt, et al.
Translational Psychiatry
|
February 12, 2019
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
Alessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, et al.
Human Genomics
|
January 24, 2026
Genetic contribution to severe COVID-19 in adults under 60 years without major comorbidities in the German National Pandemic Cohort Network (NAPKON)
Ayda Abolhassani, T Madhusankha Alawathurage, Axel Schmidt, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 24, 2021
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality
Tomoko Nakanishi, Sara Pigazzini, Frauke Degenhardt, et al.
Molecular Psychiatry
|
October 15, 2020
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia
Alessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, et al.
Communications Biology
|
November 9, 2022
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
Enrico Mingardo, Glenda Beaman, Philip Grote, et al.
Plos Pathogens
|
December 23, 2024
Systematic assessment of COVID-19 host genetics using whole genome sequencing data
Axel Schmidt, Nicolas Casadei, Fabian Brand, et al.
Page
of 21
Search research articles
Search
Showing results (191-200 of 205) with videos related to
Sort By:
Page
of 21
European Journal of Human Genetics : EJHG
|
September 12, 2013
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
Jessica Becker, Darina Czamara, Tom S Scerri, et al.
American Journal of Human Genetics
|
December 1, 2014
Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndrome
Dagmar Wieczorek, William G Newman, Thomas Wieland, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 11, 2016
Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis
Charlotte W Ockeloen, Kriti D Khandelwal, Karoline Dreesen, et al.
The Journal of Clinical Investigation
|
October 1, 2021
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality
Tomoko Nakanishi, Sara Pigazzini, Frauke Degenhardt, et al.
Translational Psychiatry
|
February 12, 2019
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
Alessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, et al.
Human Genomics
|
January 24, 2026
Genetic contribution to severe COVID-19 in adults under 60 years without major comorbidities in the German National Pandemic Cohort Network (NAPKON)
Ayda Abolhassani, T Madhusankha Alawathurage, Axel Schmidt, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 24, 2021
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality
Tomoko Nakanishi, Sara Pigazzini, Frauke Degenhardt, et al.
Molecular Psychiatry
|
October 15, 2020
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia
Alessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, et al.
Communications Biology
|
November 9, 2022
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
Enrico Mingardo, Glenda Beaman, Philip Grote, et al.
Plos Pathogens
|
December 23, 2024
Systematic assessment of COVID-19 host genetics using whole genome sequencing data
Axel Schmidt, Nicolas Casadei, Fabian Brand, et al.
Page
of 21