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Research | | Open
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Research |
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
- Stephan J. Sanders
- , Michael T. Murtha
- , Abha R. Gupta
- , John D. Murdoch
- , Melanie J. Raubeson
- , A. Jeremy Willsey
- , A. Gulhan Ercan-Sencicek
- , Nicholas M. DiLullo
- , Neelroop N. Parikshak
- , Jason L. Stein
- , Michael F. Walker
- , Gordon T. Ober
- , Nicole A. Teran
- , Youeun Song
- , Paul El-Fishawy
- , Ryan C. Murtha
- , Murim Choi
- , John D. Overton
- , Robert D. Bjornson
- , Nicholas J. Carriero
- , Kyle A. Meyer
- , Kaya Bilguvar
- , Shrikant M. Mane
- , Nenad Šestan
- , Richard P. Lifton
- , Murat Günel
- , Kathryn Roeder
- , Daniel H. Geschwind
- , Bernie Devlin
- & Matthew W. State
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Research |
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
- Daniel J Weiner
- , Emilie M Wigdor
- , Stephan Ripke
- , Raymond K Walters
- , Jack A Kosmicki
- , Jakob Grove
- , Kaitlin E Samocha
- , Jacqueline I Goldstein
- , Aysu Okbay
- , Jonas Bybjerg-Grauholm
- , Thomas Werge
- , David M Hougaard
- , Jacob Taylor
- , Marie Bækvad-Hansen
- , Ashley Dumont
- , Christine Hansen
- , Thomas F Hansen
- , Daniel Howrigan
- , Manuel Mattheisen
- , Jennifer Moran
- , Ole Mors
- , Merete Nordentoft
- , Bent Nørgaard-Pedersen
- , Timothy Poterba
- , Jesper Poulsen
- , Christine Stevens
- , Verneri Anttila
- , Peter Holmans
- , Hailiang Huang
- , Lambertus Klei
- , Phil H Lee
- , Sarah E Medland
- , Benjamin Neale
- , Lauren A Weiss
- , Lonnie Zwaigenbaum
- , Timothy W Yu
- , Kerstin Wittemeyer
- , A Jeremy Willsey
- , Ellen M Wijsman
- , Thomas H Wassink
- , Regina Waltes
- , Christopher A Walsh
- , Simon Wallace
- , Jacob A S Vorstman
- , Veronica J Vieland
- , Astrid M Vicente
- , Herman van Engeland
- , Kathryn Tsang
- , Ann P Thompson
- , Peter Szatmari
- , Oscar Svantesson
- , Stacy Steinberg
- , Kari Stefansson
- , Hreinn Stefansson
- , Matthew W State
- , Latha Soorya
- , Teimuraz Silagadze
- , Stephen W Scherer
- , Gerard D Schellenberg
- , Sven Sandin
- , Evald Saemundsen
- , Guy A Rouleau
- , Bernadette Rogé
- , Kathryn Roeder
- , Wendy Roberts
- , Jennifer Reichert
- , Abraham Reichenberg
- , Karola Rehnström
- , Regina Regan
- , Fritz Poustka
- , Christopher S Poultney
- , Joseph Piven
- , Dalila Pinto
- , Margaret A Pericak-Vance
- , Milica Pejovic-Milovancevic
- , Marianne G Pedersen
- , Carsten B Pedersen
- , Andrew D Paterson
- , Jeremy R Parr
- , Alistair T Pagnamenta
- , Guiomar Oliveira
- , John I Nurnberger
- , Merete Nordentoft
- , Michael T Murtha
- , Susana Mouga
- , Ole Mors
- , Eric M Morrow
- , Daniel Moreno De Luca
- , Anthony P Monaco
- , Nancy Minshew
- , Alison Merikangas
- , William M McMahon
- , Susan G McGrew
- , Manuel Mattheisen
- , Igor Martsenkovsky
- , Donna M Martin
- , Shrikant M Mane
- , Pall Magnusson
- , Tiago Magalhaes
- , Elena Maestrini
- , Jennifer K Lowe
- , Catherine Lord
- , Pat Levitt
- , Christa Lese Martin
- , David H Ledbetter
- , Marion Leboyer
- , Ann S Le Couteur
- , Christine Ladd-Acosta
- , Alexander Kolevzon
- , Sabine M Klauck
- , Suma Jacob
- , Bozenna Iliadou
- , Christina M Hultman
- , Irva Hertz-Picciotto
- , Robert Hendren
- , Christine S Hansen
- , Jonathan L Haines
- , Stephen J Guter
- , Dorothy E Grice
- , Jonathan M Green
- , Andrew Green
- , Arthur P Goldberg
- , Christopher Gillberg
- , John Gilbert
- , Louise Gallagher
- , Christine M Freitag
- , Eric Fombonne
- , Susan E Folstein
- , Bridget Fernandez
- , M Daniele Fallin
- , A Gulhan Ercan-Sencicek
- , Sean Ennis
- , Frederico Duque
- , Eftichia Duketis
- , Richard Delorme
- , Silvia De Rubeis
- , Maretha V De Jonge
- , Geraldine Dawson
- , Michael L Cuccaro
- , Catarina T Correia
- , Judith Conroy
- , Inês C Conceição
- , Andreas G Chiocchetti
- , Patrícia B S Celestino-Soper
- , Jillian Casey
- , Rita M Cantor
- , Cátia Café
- , Sean Brennan
- , Thomas Bourgeron
- , Patrick F Bolton
- , Sven Bölte
- , Nadia Bolshakova
- , Catalina Betancur
- , Raphael Bernier
- , Arthur L Beaudet
- , Agatino Battaglia
- , Vanessa H Bal
- , Gillian Baird
- , Anthony J Bailey
- , Marie Bækvad-Hansen
- , Joel S Bader
- , Elena Bacchelli
- , Evdokia Anagnostou
- , David Amaral
- , Joana Almeida
- , Joseph D Buxbaum
- , Aravinda Chakravarti
- , Edwin H Cook
- , Hilary Coon
- , Daniel H Geschwind
- , Michael Gill
- , Hakon Hakonarson
- , Joachim Hallmayer
- , Aarno Palotie
- , Susan Santangelo
- , James S Sutcliffe
- , Dan E Arking
- , David Skuse
- , Bernie Devlin
- , Richard Anney
- , Stephan J Sanders
- , Somer Bishop
- , Preben Bo Mortensen
- , Anders D Børglum
- , George Davey Smith
- , Mark J Daly
- & Elise B Robinson
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Research |
Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas
- Victoria E Clark
- , Akdes Serin Harmancı
- , Hanwen Bai
- , Mark W Youngblood
- , Tong Ihn Lee
- , Jacob F Baranoski
- , A Gulhan Ercan-Sencicek
- , Brian J Abraham
- , Abraham S Weintraub
- , Denes Hnisz
- , Matthias Simon
- , Boris Krischek
- , E Zeynep Erson-Omay
- , Octavian Henegariu
- , Geneive Carrión-Grant
- , Ketu Mishra-Gorur
- , Daniel Durán
- , Johanna E Goldmann
- , Johannes Schramm
- , Roland Goldbrunner
- , Joseph M Piepmeier
- , Alexander O Vortmeyer
- , Jennifer Moliterno Günel
- , Kaya Bilgüvar
- , Katsuhito Yasuno
- , Richard A Young
- & Murat Günel
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Research |
Integrated genomic characterization of IDH1-mutant glioma malignant progression
- Hanwen Bai
- , Akdes Serin Harmancı
- , E Zeynep Erson-Omay
- , Jie Li
- , Süleyman Coşkun
- , Matthias Simon
- , Boris Krischek
- , Koray Özduman
- , S Bülent Omay
- , Eric A Sorensen
- , Şevin Turcan
- , Mehmet Bakırcığlu
- , Geneive Carrión-Grant
- , Phillip B Murray
- , Victoria E Clark
- , A Gulhan Ercan-Sencicek
- , James Knight
- , Leman Sencar
- , Selin Altınok
- , Leon D Kaulen
- , Burcu Gülez
- , Marco Timmer
- , Johannes Schramm
- , Ketu Mishra-Gorur
- , Octavian Henegariu
- , Jennifer Moliterno
- , Angeliki Louvi
- , Timothy A Chan
- , Stacey L Tannheimer
- , M Necmettin Pamir
- , Alexander O Vortmeyer
- , Kaya Bilguvar
- , Katsuhito Yasuno
- & Murat Günel
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Research |
Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans
- A Gulhan Ercan-Sencicek
- , Samira Jambi
- , Daniel Franjic
- , Sayoko Nishimura
- , Mingfeng Li
- , Paul El-Fishawy
- , Thomas M Morgan
- , Stephan J Sanders
- , Kaya Bilguvar
- , Mohnish Suri
- , Michele H Johnson
- , Abha R Gupta
- , Zafer Yuksel
- , Shrikant Mane
- , Elena Grigorenko
- , Marina Picciotto
- , Arthur S Alberts
- , Murat Gunel
- , Nenad Šestan
- & Matthew W State
