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Aniko Sabo

Showing results (41-50 of 52) with videos related to

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Hepatology (Baltimore, Md.)|January 22, 2019
Identification of Polycystic Kidney Disease 1 Like 1 Gene Variants in Children With Biliary Atresia Splenic Malformation SyndromeJohn-Paul Berauer, Anya I Mezina, David T Okou, et al.
American Journal of Medical Genetics. Part A|March 21, 2023
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variantsPagna Sok, Aniko Sabo, Lynn M Almli, et al.
Neuron|January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disordersElaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 7, 2021
Genetic testing in ambulatory cardiology clinics reveals high rate of findings with clinical management implicationsDavid R Murdock, Eric Venner, Donna M Muzny, et al.
Nature|April 13, 2012
Patterns and rates of exonic de novo mutations in autism spectrum disordersBenjamin M Neale, Yan Kou, Li Liu, et al.
Nature|October 25, 2008
Somatic mutations affect key pathways in lung adenocarcinomaLi Ding, Gad Getz, David A Wheeler, et al.
Nature|November 4, 2014
Synaptic, transcriptional and chromatin genes disrupted in autismSilvia De Rubeis, Xin He, Arthur P Goldberg, et al.
NPJ Aging and Mechanisms of Disease|July 20, 2017
Fine mapping the <i>CETP</i> region reveals a common intronic insertion associated to HDL-CElisabeth M van Leeuwen, Jennifer E Huffman, Joshua C Bis, et al.
Journal of Medical Genetics|April 3, 2016
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levelsElisabeth M van Leeuwen, Aniko Sabo, Joshua C Bis, et al.
Nature|April 9, 2005
Generation and annotation of the DNA sequences of human chromosomes 2 and 4Ladeana W Hillier, Tina A Graves, Robert S Fulton, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Hepatology (Baltimore, Md.)|January 22, 2019
Identification of Polycystic Kidney Disease 1 Like 1 Gene Variants in Children With Biliary Atresia Splenic Malformation SyndromeJohn-Paul Berauer, Anya I Mezina, David T Okou, et al.
American Journal of Medical Genetics. Part A|March 21, 2023
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variantsPagna Sok, Aniko Sabo, Lynn M Almli, et al.
Neuron|January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disordersElaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 7, 2021
Genetic testing in ambulatory cardiology clinics reveals high rate of findings with clinical management implicationsDavid R Murdock, Eric Venner, Donna M Muzny, et al.
Nature|April 13, 2012
Patterns and rates of exonic de novo mutations in autism spectrum disordersBenjamin M Neale, Yan Kou, Li Liu, et al.
Nature|October 25, 2008
Somatic mutations affect key pathways in lung adenocarcinomaLi Ding, Gad Getz, David A Wheeler, et al.
Nature|November 4, 2014
Synaptic, transcriptional and chromatin genes disrupted in autismSilvia De Rubeis, Xin He, Arthur P Goldberg, et al.
NPJ Aging and Mechanisms of Disease|July 20, 2017
Fine mapping the <i>CETP</i> region reveals a common intronic insertion associated to HDL-CElisabeth M van Leeuwen, Jennifer E Huffman, Joshua C Bis, et al.
Journal of Medical Genetics|April 3, 2016
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levelsElisabeth M van Leeuwen, Aniko Sabo, Joshua C Bis, et al.
Nature|April 9, 2005
Generation and annotation of the DNA sequences of human chromosomes 2 and 4Ladeana W Hillier, Tina A Graves, Robert S Fulton, et al.
Pageof 6