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



Raphael Bernier, Kyle J Steinman, Beau Reilly, Arianne Stevens Wallace, Elliott H Sherr, Nicholas Pojman, Heather C Mefford, Jennifer Gerdts, Rachel Earl, Ellen Hanson, Robin P Goin-Kochel, Leandra Berry, Stephen Kanne, LeeAnne Green Snyder, Sarah Spence, Melissa B Ramocki, David W Evans, John E Spiro, Christa L Martin, David H Ledbetter, Wendy K Chung. Genet Med 2016
Times Cited: 72




List of shared articles



Times cited

Clinical characterization of individuals with the distal 1q21.1 microdeletion.
Stacey D Edwards, Katharina V Schulze, Jill A Rosenfeld, Lauren E Westerfield, Amanda Gerard, Bo Yuan, Elena L Grigorenko, Jennifer E Posey, Weimin Bi, Pengfei Liu. Am J Med Genet A 2021
0

Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs.
Ida E Sønderby, Christopher R K Ching, Sophia I Thomopoulos, Dennis van der Meer, Daqiang Sun, Julio E Villalon-Reina, Ingrid Agartz, Katrin Amunts, Celso Arango, Nicola J Armstrong,[...]. Hum Brain Mapp 2021
0

Chromosomal microarray analysis in fetuses with high-risk prenatal indications: A retrospective study in China.
Xiaomei Luo, Hong Zhu, Lili Wang, Bing Xiao, Yanjie Fan, Hui Ye, Xiaomin Ying, Wenjuan Qiu, Huiwen Zhang, Lianshu Han,[...]. Taiwan J Obstet Gynecol 2021
0

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans.
Ida E Sønderby, Dennis van der Meer, Clara Moreau, Tobias Kaufmann, G Bragi Walters, Maria Ellegaard, Abdel Abdellaoui, David Ames, Katrin Amunts, Micael Andersson,[...]. Transl Psychiatry 2021
1

Prenatally detected copy number variants in a national cohort: A postnatal follow-up study.
Joke Muys, Yves Jacquemyn, Bettina Blaumeiser, Laura Bourlard, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Anne De Leener, Marjan De Rademaeker, Julie Désir,[...]. Prenat Diagn 2020
1

Genetic mechanisms of neurodevelopmental disorders.
P Y Billie Au, Alison Eaton, David A Dyment. Handb Clin Neurol 2020
0

An estimation of the prevalence of genomic disorders using chromosomal microarray data.
Madelyn A Gillentine, Philip J Lupo, Pawel Stankiewicz, Christian P Schaaf. J Hum Genet 2018
14

Prenatal Diagnosis of Recurrent Distal 1q21.1 Duplication in Three Fetuses With Ultrasound Anomalies.
Xiuqing Ji, Qiong Pan, Yan Wang, Yun Wu, Jing Zhou, An Liu, Fengchang Qiao, Dingyuan Ma, Ping Hu, Zhengfeng Xu. Front Genet 2018
2