Search research articles
Contact Us
Filters
Showing results (21-30 of 35) with videos related to
Page
of 4
Sort By:
European Journal of Human Genetics : EJHG
|
March 23, 2017
PUF60 variants cause a syndrome of ID, short stature, microcephaly, coloboma, craniofacial, cardiac, renal and spinal features
Karen J Low, Morad Ansari, Rami Abou Jamra, et al.
Human Mutation
|
July 18, 2025
Whole Genome Sequencing of "Mutation-Negative" Individuals With Cornelia de Lange Syndrome
Morad Ansari, Mihail Halachev, David Parry, et al.
Brain : a Journal of Neurology
|
January 13, 2024
Novel loss-of-function variants expand ABCC9-related intellectual disability and myopathy syndrome
Stephanie Efthymiou, Marcello Scala, Vini Nagaraj, et al.
Human Molecular Genetics
|
July 23, 2013
Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degeneration
Morad Ansari, Paul M McKeigue, Christine Skerka, et al.
Nature Genetics
|
October 6, 2015
Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families
Nadia Akawi, Jeremy McRae, Morad Ansari, et al.
Plos Biology
|
December 15, 2020
A sensitive and affordable multiplex RT-qPCR assay for SARS-CoV-2 detection
Martin A M Reijns, Louise Thompson, Juan Carlos Acosta, et al.
Plos One
|
January 26, 2010
Concordant association of insulin degrading enzyme gene (IDE) variants with IDE mRNA, Abeta, and Alzheimer's disease
Minerva M Carrasquillo, Olivia Belbin, Fanggeng Zou, et al.
Medrxiv : the Preprint Server for Health Sciences
|
October 9, 2023
Heterozygous loss-of-function <i>SMC3</i> variants are associated with variable and incompletely penetrant growth and developmental features
Morad Ansari, Kamli N W Faour, Akiko Shimamura, et al.
Plos One
|
April 29, 2016
Genetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie Syndrome
Morad Ansari, Jacqueline Rainger, Isabel M Hanson, et al.
HGG Advances
|
February 1, 2024
Heterozygous loss-of-function SMC3 variants are associated with variable growth and developmental features
Morad Ansari, Kamli N W Faour, Akiko Shimamura, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 35) with videos related to
Sort By:
Page
of 4
European Journal of Human Genetics : EJHG
|
March 23, 2017
PUF60 variants cause a syndrome of ID, short stature, microcephaly, coloboma, craniofacial, cardiac, renal and spinal features
Karen J Low, Morad Ansari, Rami Abou Jamra, et al.
Human Mutation
|
July 18, 2025
Whole Genome Sequencing of "Mutation-Negative" Individuals With Cornelia de Lange Syndrome
Morad Ansari, Mihail Halachev, David Parry, et al.
Brain : a Journal of Neurology
|
January 13, 2024
Novel loss-of-function variants expand ABCC9-related intellectual disability and myopathy syndrome
Stephanie Efthymiou, Marcello Scala, Vini Nagaraj, et al.
Human Molecular Genetics
|
July 23, 2013
Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degeneration
Morad Ansari, Paul M McKeigue, Christine Skerka, et al.
Nature Genetics
|
October 6, 2015
Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families
Nadia Akawi, Jeremy McRae, Morad Ansari, et al.
Plos Biology
|
December 15, 2020
A sensitive and affordable multiplex RT-qPCR assay for SARS-CoV-2 detection
Martin A M Reijns, Louise Thompson, Juan Carlos Acosta, et al.
Plos One
|
January 26, 2010
Concordant association of insulin degrading enzyme gene (IDE) variants with IDE mRNA, Abeta, and Alzheimer's disease
Minerva M Carrasquillo, Olivia Belbin, Fanggeng Zou, et al.
Medrxiv : the Preprint Server for Health Sciences
|
October 9, 2023
Heterozygous loss-of-function <i>SMC3</i> variants are associated with variable and incompletely penetrant growth and developmental features
Morad Ansari, Kamli N W Faour, Akiko Shimamura, et al.
Plos One
|
April 29, 2016
Genetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie Syndrome
Morad Ansari, Jacqueline Rainger, Isabel M Hanson, et al.
HGG Advances
|
February 1, 2024
Heterozygous loss-of-function SMC3 variants are associated with variable growth and developmental features
Morad Ansari, Kamli N W Faour, Akiko Shimamura, et al.
Page
of 4