Publications by authors named "Xander Nuttle"

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Activation of the imprinted Prader-Willi syndrome locus by CRISPR-based epigenome editing.
Dahlia Rohm, Joshua B Black, Sean R McCutcheon, Alejandro Barrera, Shanté S Berry, Xander Nuttle

Cell Genom· February 2025

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Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models.
Derek J C Tai, Parisa Razaz, Serkan Erdin, Dadi Gao, Jennifer Wang, Xander Nuttle

Am J Hum Genet· March 2024

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Activation of the imprinted Prader-Willi Syndrome locus by CRISPR-based epigenome editing.
Dahlia Rohm, Joshua B Black, Sean R McCutcheon, Alejandro Barrera, Daniel J Morone, Xander Nuttle

bioRxiv· March 2024

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Parallelized engineering of mutational models using piggyBac transposon delivery of CRISPR libraries.
Xander Nuttle, Nicholas D Burt, Benjamin Currall, Mariana Moysés-Oliveira, Kiana Mohajeri

Cell Rep Methods· January 2024

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Author Correction: Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts.
Giuliana Giannuzzi, Nicolas Chatron, Katrin Mannik, Chiara Auwerx, Sylvain Pradervand, Xander Nuttle

NPJ Genom Med· May 2023

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Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies.
Calwing Liao, Mariana Moyses-Oliveira, Celine E F De Esch, Riya Bhavsar, Xander Nuttle

Cell Genom· April 2023

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Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models.
Derek J C Tai, Parisa Razaz, Serkan Erdin, Dadi Gao, Jennifer Wang, Xander Nuttle

Am J Hum Genet· October 2022

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A cross-disorder dosage sensitivity map of the human genome.
Ryan L Collins, Joseph T Glessner, Eleonora Porcu, Maarja Lepamets, Rhonda Brandon, Xander Nuttle

Cell· August 2022

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Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts.
Giuliana Giannuzzi, Nicolas Chatron, Katrin Mannik, Chiara Auwerx, Sylvain Pradervand, Xander Nuttle

NPJ Genom Med· June 2022

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The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals.
Giuliana Giannuzzi, Paul J Schmidt, Eleonora Porcu, Gilles Willemin, Katherine M Munson, Xander Nuttle

Am J Hum Genet· November 2019

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Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical Neurogenesis.
Ian T Fiddes, Gerrald A Lodewijk, Meghan Mooring, Colleen M Bosworth, Adam D Ewing, Xander Nuttle

Cell· May 2018

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Longitudinal report of child with de novo 16p11.2 triplication.
Arianne S Wallace, Caitlin M Hudac, Kyle J Steinman, Jessica L Peterson, Trent D DesChamps, Xander Nuttle

Clin Case Rep· January 2018

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The birth of a human-specific neural gene by incomplete duplication and gene fusion.
Max L Dougherty, Xander Nuttle, Osnat Penn, Bradley J Nelson, John Huddleston

Genome Biol· March 2017

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The evolution and population diversity of human-specific segmental duplications.
Megan Y Dennis, Lana Harshman, Bradley J Nelson, Osnat Penn, Stuart Cantsilieris, Xander Nuttle

Nat Ecol Evol· February 2017

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Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility.
Xander Nuttle, Giuliana Giannuzzi, Michael H Duyzend, Joshua G Schraiber, Iñigo Narvaiza

Nature· August 2016

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Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV.
Michael H Duyzend, Xander Nuttle, Bradley P Coe, Carl Baker, Deborah A Nickerson

Am J Hum Genet· January 2016

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Resolving genomic disorder-associated breakpoints within segmental DNA duplications using massively parallel sequencing.
Xander Nuttle, Andy Itsara, Jay Shendure, Evan E Eichler

Nat Protoc· December 2014

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Rapid and accurate large-scale genotyping of duplicated genes and discovery of interlocus gene conversions.
Xander Nuttle, John Huddleston, Brian J O'Roak, Francesca Antonacci, Marco Fichera

Nat Methods· September 2013

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Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplication.
Megan Y Dennis, Xander Nuttle, Peter H Sudmant, Francesca Antonacci, Tina A Graves

Cell· May 2012

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