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https://cellecta.net/drivermap-air-genres-230201-468x60

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Research

ZAK as a cause of limb defects in humans and mice" > Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and mice

Malte Spielmann
Naseebullah Kakar
Naeimeh Tayebi
Catherine Leettola
Gudrun Nürnberg
Nadine Sowada Darío G. Lupiáñez Izabela Harabula Ricarda Flöttmann Denise Horn Wing Lee Chan Lars Wittler Rüstem Yilmaz Janine Altmüller Holger Thiele Hans van Bokhoven Charles E. Schwartz Peter Nürnberg James U. Bowie
... [+14 authors] ...,
Jamil Ahmad
Christian Kubisch
Stefan Mundlos
Guntram Borck

First Published January 11, 2016

Research

Coding exons function as tissue-specific enhancers of nearby genes

Ramon Y. Birnbaum
E. Josephine Clowney
Orly Agamy
Mee J. Kim
Jingjing Zhao
Takayuki Yamanaka Zachary Pappalardo Shoa L. Clarke Aaron M. Wenger Loan Nguyen Fiorella Gurrieri David B. Everman Charles E. Schwartz
... [+8 authors] ...,
Ohad S. Birk
Gill Bejerano
Stavros Lomvardas
Nadav Ahituv

First Published March 22, 2012

Methods

A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease

Heather C. Mefford
Gregory M. Cooper
Troy Zerr
Joshua D. Smith
Carl Baker
Neil Shafer Erik C. Thorland
... [+2 authors] ...,
Cindy Skinner
Charles E. Schwartz
Deborah A. Nickerson
Evan E. Eichler

First Published June 8, 2009

LETTER

MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair" > Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair

Marijke Bauters
Hilde Van Esch
Michael J. Friez
Odile Boespflug-Tanguy
Martin Zenker
Angela M. Vianna-Morgante Carla Rosenberg Jaakko Ignatius Martine Raynaud Karen Hollanders Karen Govaerts Kris Vandenreijt Florence Niel Pierre Blanc Roger E. Stevenson
... [+10 authors] ...,
Jean-Pierre Fryns
Peter Marynen
Charles E. Schwartz
Guy Froyen

First Published April 2, 2008

Methods

PLP2 promoter polymorphism enriched in patients with X-linked mental retardation" > X chromosome cDNA microarray screening identifies a functional PLP2 promoter polymorphism enriched in patients with X-linked mental retardation

Lilei Zhang
Chunfa Jie
Cassandra Obie
Fatima Abidi
Charles E. Schwartz
Roger E. Stevenson
David Valle
Tao Wang

First Published April 6, 2007