Showing results (1601-1610 of 1,657) with videos related to

Sort By:
Pageof 166
Nature|May 14, 2013
De novo mutations in histone-modifying genes in congenital heart diseaseSamir Zaidi, Murim Choi, Hiroko Wakimoto, et al.
JAMA Neurology|June 14, 2021
DIAPH1 Variants in Non-East Asian Patients With Sporadic Moyamoya DiseaseAdam J Kundishora, Samuel T Peters, Amélie Pinard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2025
Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT familiesLea Maria Merz, Caroline M Kolvenbach, Chunyan Wang, et al.
Schizophrenia Research|October 11, 2025
Polygenic risk score of glycemic homeostasis, Type 2 Diabetes Mellitus and glycemic components in first episode psychosisAlex G Segura, Norma Verdolini, Isabel Valli, et al.
Neuron|September 25, 2015
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk LociStephan J Sanders, Xin He, A Jeremy Willsey, et al.
Vaccine|June 20, 2020
Intussusception in children aged under two years in India: Retrospective surveillance at nineteen tertiary care hospitalsManoja Kumar Das, Narendra Kumar Arora, Bini Gupta, et al.
Frontiers in Microbiology|December 22, 2025
Multicenter epidemiology of <i>Stenotrophomonas maltophilia</i> bloodstream infections in Indian ICUs: building digital surveillance networkParul Singh, M Nizam Ahmed, Ashish Kumar Srivastava, et al.
The Journal of Clinical Investigation|September 5, 2018
Mutations in multiple components of the nuclear pore complex cause nephrotic syndromeDaniela A Braun, Svjetlana Lovric, David Schapiro, et al.
Clinical Journal of the American Society of Nephrology : CJASN|November 12, 2017
Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic SyndromeJillian K Warejko, Weizhen Tan, Ankana Daga, et al.
Nature Medicine|October 20, 2020
Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalusSheng Chih Jin, Weilai Dong, Adam J Kundishora, et al.
Pageof 166