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Xander Nuttle

Showing results (11-20 of 19) with videos related to

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Cell Genomics|April 21, 2023
Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studiesCalwing Liao, Mariana Moyses-Oliveira, Celine E F De Esch, et al.
American Journal of Human Genetics|November 1, 2019
The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism IndividualsGiuliana Giannuzzi, Paul J Schmidt, Eleonora Porcu, et al.
Nature Ecology & Evolution|June 6, 2017
The evolution and population diversity of human-specific segmental duplicationsMegan Y Dennis, Lana Harshman, Bradley J Nelson, et al.
American Journal of Human Genetics|September 24, 2022
Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal modelsDerek J C Tai, Parisa Razaz, Serkan Erdin, et al.
Cell|June 2, 2018
Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical NeurogenesisIan T Fiddes, Gerrald A Lodewijk, Meghan Mooring, et al.
Nature|August 4, 2016
Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibilityXander Nuttle, Giuliana Giannuzzi, Michael H Duyzend, et al.
Cell|August 2, 2022
A cross-disorder dosage sensitivity map of the human genomeRyan L Collins, Joseph T Glessner, Eleonora Porcu, et al.
Medrxiv : the Preprint Server for Health Sciences|March 11, 2026
Clinical, <i>in vitro,</i> and <i>in vivo</i> evidence of <i>WAPL</i> as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorderPhilip M Boone, Serkan Erdin, Abucar Mohamed, et al.
American Journal of Human Genetics|July 10, 2026
Clinical, in vitro, and in vivo evidence of WAPL as a cohesinopathy-associated gene and phenotypic driver of 10q22.3q23.2 genomic disorderPhilip M Boone, Serkan Erdin, Abucar Mohamed, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Cell Genomics|April 21, 2023
Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studiesCalwing Liao, Mariana Moyses-Oliveira, Celine E F De Esch, et al.
American Journal of Human Genetics|November 1, 2019
The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism IndividualsGiuliana Giannuzzi, Paul J Schmidt, Eleonora Porcu, et al.
Nature Ecology & Evolution|June 6, 2017
The evolution and population diversity of human-specific segmental duplicationsMegan Y Dennis, Lana Harshman, Bradley J Nelson, et al.
American Journal of Human Genetics|September 24, 2022
Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal modelsDerek J C Tai, Parisa Razaz, Serkan Erdin, et al.
Cell|June 2, 2018
Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical NeurogenesisIan T Fiddes, Gerrald A Lodewijk, Meghan Mooring, et al.
Nature|August 4, 2016
Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibilityXander Nuttle, Giuliana Giannuzzi, Michael H Duyzend, et al.
Cell|August 2, 2022
A cross-disorder dosage sensitivity map of the human genomeRyan L Collins, Joseph T Glessner, Eleonora Porcu, et al.
Medrxiv : the Preprint Server for Health Sciences|March 11, 2026
Clinical, <i>in vitro,</i> and <i>in vivo</i> evidence of <i>WAPL</i> as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorderPhilip M Boone, Serkan Erdin, Abucar Mohamed, et al.
American Journal of Human Genetics|July 10, 2026
Clinical, in vitro, and in vivo evidence of WAPL as a cohesinopathy-associated gene and phenotypic driver of 10q22.3q23.2 genomic disorderPhilip M Boone, Serkan Erdin, Abucar Mohamed, et al.
Pageof 2