A citation-based method for searching scientific literature

Jill A Rosenfeld, Bradley P Coe, Evan E Eichler, Howard Cuckle, Lisa G Shaffer. Genet Med 2013
Times Cited: 174



Debra D'Angelo, Sébastien Lebon, Qixuan Chen, Sandra Martin-Brevet, LeeAnne Green Snyder, Loyse Hippolyte, Ellen Hanson, Anne M Maillard, W Andrew Faucett, Aurélien Macé, Aurélie Pain, Raphael Bernier, Samuel J R A Chawner, Albert David, Joris Andrieux, Elizabeth Aylward, Genevieve Baujat, Ines Caldeira, Philippe Conus, Carrina Ferrari, Francesca Forzano, Marion Gérard, Robin P Goin-Kochel, Ellen Grant, Jill V Hunter, Bertrand Isidor, Aurélia Jacquette, Aia E Jønch, Boris Keren, Didier Lacombe, Cédric Le Caignec, Christa Lese Martin, Katrin Männik, Andres Metspalu, Cyril Mignot, Pratik Mukherjee, Michael J Owen, Marzia Passeggeri, Caroline Rooryck-Thambo, Jill A Rosenfeld, Sarah J Spence, Kyle J Steinman, Jennifer Tjernagel, Mieke Van Haelst, Yiping Shen, Bogdan Draganski, Elliott H Sherr, David H Ledbetter, Marianne B M van den Bree, Jacques S Beckmann, John E Spiro, Alexandre Reymond, Sébastien Jacquemont, Wendy K Chung. JAMA Psychiatry 2016
Times Cited: 99




List of shared articles



Times cited

Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents.
Dinka Smajlagić, Ksenia Lavrichenko, Siren Berland, Øyvind Helgeland, Gun Peggy Knudsen, Marc Vaudel, Jan Haavik, Per Morten Knappskog, Pål Rasmus Njølstad, Gunnar Houge,[...]. Eur J Hum Genet 2021
2

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

Genetic Advances in Autism.
Anita Thapar, Michael Rutter. J Autism Dev Disord 2020
5

16p11.2 Copy Number Variations and Neurodevelopmental Disorders.
Benjamin Rein, Zhen Yan. Trends Neurosci 2020
3

Distal chromosome 16p11.2 duplications containing SH2B1 in patients with scoliosis.
Brooke Sadler, Gabe Haller, Lilian Antunes, Xavier Bledsoe, Jose Morcuende, Philip Giampietro, Cathleen Raggio, Nancy Miller, Yared Kidane, Carol A Wise,[...]. J Med Genet 2019
4

Estimating the effect size of the 15Q11.2 BP1-BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice.
Aia Elise Jønch, Elise Douard, Clara Moreau, Anke Van Dijck, Marzia Passeggeri, Frank Kooy, Jacques Puechberty, Carolyn Campbell, Damien Sanlaville, Henrietta Lefroy,[...]. J Med Genet 2019
13

Focal Cortical Anomalies and Language Impairment in 16p11.2 Deletion and Duplication Syndrome.
Karen Blackmon, Thomas Thesen, Sophie Green, Emma Ben-Avi, Xiuyuan Wang, Benjamin Fuchs, Ruben Kuzniecky, Orrin Devinsky. Cereb Cortex 2018
10

16p11.2 transcription factor MAZ is a dosage-sensitive regulator of genitourinary development.
Meade Haller, Jason Au, Marisol O'Neill, Dolores J Lamb. Proc Natl Acad Sci U S A 2018
14