A citation-based method for searching scientific literature

Santhosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, Francesca Antonacci, Priscillia Siswara, Andy Itsara, Laura Vives, Tom Walsh, Shane E McCarthy, Carl Baker, Heather C Mefford, Jeffrey M Kidd, Sharon R Browning, Brian L Browning, Diane E Dickel, Deborah L Levy, Blake C Ballif, Kathryn Platky, Darren M Farber, Gordon C Gowans, Jessica J Wetherbee, Alexander Asamoah, David D Weaver, Paul R Mark, Jennifer Dickerson, Bhuwan P Garg, Sara A Ellingwood, Rosemarie Smith, Valerie C Banks, Wendy Smith, Marie T McDonald, Joe J Hoo, Beatrice N French, Cindy Hudson, John P Johnson, Jillian R Ozmore, John B Moeschler, Urvashi Surti, Luis F Escobar, Dima El-Khechen, Jerome L Gorski, Jennifer Kussmann, Bonnie Salbert, Yves Lacassie, Alisha Biser, Donna M McDonald-McGinn, Elaine H Zackai, Matthew A Deardorff, Tamim H Shaikh, Eric Haan, Kathryn L Friend, Marco Fichera, Corrado Romano, Jozef Gécz, Lynn E DeLisi, Jonathan Sebat, Mary-Claire King, Lisa G Shaffer, Evan E Eichler. Nat Genet 2010
Times Cited: 411



Brian J O'Roak, Pelagia Deriziotis, Choli Lee, Laura Vives, Jerrod J Schwartz, Santhosh Girirajan, Emre Karakoc, Alexandra P Mackenzie, Sarah B Ng, Carl Baker, Mark J Rieder, Deborah A Nickerson, Raphael Bernier, Simon E Fisher, Jay Shendure, Evan E Eichler. Nat Genet 2011
Times Cited: 754




List of shared articles



Times cited

Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriers.
Caitlin M Hudac, Joanna Bove, Shelley Barber, Michael Duyzend, Ari Wallace, Christa Lese Martin, David H Ledbetter, Ellen Hanson, Robin P Goin-Kochel, LeeAnne Green-Snyder,[...]. Autism Res 2020
5


Characterization of intellectual disability and autism comorbidity through gene panel sequencing.
Maria C Aspromonte, Mariagrazia Bellini, Alessandra Gasparini, Marco Carraro, Elisa Bettella, Roberta Polli, Federica Cesca, Stefania Bigoni, Stefania Boni, Ombretta Carlet,[...]. Hum Mutat 2019
15

Identification of putative second genetic hits in schizophrenia carriers of high-risk copy number variants and resequencing in additional samples.
Julio Rodríguez-López, Beatriz Sobrino, Jorge Amigo, Noa Carrera, Julio Brenlla, Santiago Agra, Eduardo Paz, Ángel Carracedo, Mario Páramo, Manuel Arrojo,[...]. Eur Arch Psychiatry Clin Neurosci 2018
2

Copy Number Variation Analysis of 100 Twin Pairs Enriched for Neurodevelopmental Disorders.
Sofia Stamouli, Britt-Marie Anderlid, Charlotte Willfors, Bhooma Thiruvahindrapuram, John Wei, Steve Berggren, Ann Nordgren, Stephen W Scherer, Paul Lichtenstein, Kristiina Tammimies,[...]. Twin Res Hum Genet 2018
14

Association study and mutation sequencing of genes on chromosome 15q11-q13 identified GABRG3 as a susceptibility gene for autism in Chinese Han population.
Linyan Wang, Jun Li, Mei Shuang, Tianlan Lu, Ziqi Wang, Tian Zhang, Weihua Yue, Meixiang Jia, Yanyan Ruan, Jing Liu,[...]. Transl Psychiatry 2018
2


Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model.
Hui Guo, Tianyun Wang, Huidan Wu, Min Long, Bradley P Coe, Honghui Li, Guanglei Xun, Jianjun Ou, Biyuan Chen, Guiqin Duan,[...]. Mol Autism 2018
38

Anatomy and Cell Biology of Autism Spectrum Disorder: Lessons from Human Genetics.
Kristel T E Kleijer, Guillaume Huguet, Julie Tastet, Thomas Bourgeron, J P H Burbach. Adv Anat Embryol Cell Biol 2017
7

Genomic Patterns of De Novo Mutation in Simplex Autism.
Tychele N Turner, Bradley P Coe, Diane E Dickel, Kendra Hoekzema, Bradley J Nelson, Michael C Zody, Zev N Kronenberg, Fereydoun Hormozdiari, Archana Raja, Len A Pennacchio,[...]. Cell 2017
134

Distal 22q11.2 Microduplication: Case Report and Review of the Literature.
Elana Pinchefsky, Laurence Laneuville, Myriam Srour. Child Neurol Open 2017
7