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



Carolien G F de Kovel, Holger Trucks, Ingo Helbig, Heather C Mefford, Carl Baker, Costin Leu, Christian Kluck, Hiltrud Muhle, Sarah von Spiczak, Philipp Ostertag, Tanja Obermeier, Ailing A Kleefuss-Lie, Kerstin Hallmann, Michael Steffens, Verena Gaus, Karl M Klein, Hajo M Hamer, Felix Rosenow, Eva H Brilstra, Dorothée Kasteleijn-Nolst Trenité, Marielle E M Swinkels, Yvonne G Weber, Iris Unterberger, Fritz Zimprich, Lydia Urak, Martha Feucht, Karoline Fuchs, Rikke S Møller, Helle Hjalgrim, Peter De Jonghe, Arvid Suls, Ina-Maria Rückert, Heinz-Erich Wichmann, Andre Franke, Stefan Schreiber, Peter Nürnberg, Christian E Elger, Holger Lerche, Ulrich Stephani, Bobby P C Koeleman, Dick Lindhout, Evan E Eichler, Thomas Sander. Brain 2010
Times Cited: 302




List of shared articles



Times cited

Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age.
Xiaoqing Wu, Gang An, Xiaorui Xie, Linjuan Su, Meiying Cai, Xuemei Chen, Ying Li, Na Lin, Deqin He, Meiying Wang,[...]. J Clin Lab Anal 2020
5

Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK Biobank.
Simon G Williams, Apostol Nakev, Hui Guo, Simon Frain, Gennadiy Tenin, Anna Liakhovitskaia, Priyanka Saha, James R Priest, Kathryn E Hentges, Bernard D Keavney. Eur J Hum Genet 2020
2

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

Copy number variation in genetic epilepsy with febrile seizures plus.
Olivier Fortin, Christian Vincelette, Sébastien Chénier, Ahmad Ghais, Michael I Shevell, Elisabeth Simard-Tremblay, Kenneth A Myers. Eur J Paediatr Neurol 2020
2

Should We Report 15q11.2 BP1-BP2 Deletions and Duplications in the Prenatal Setting?
Idit Maya, Sharon Perlman, Mordechai Shohat, Sarit Kahana, Shiri Yacobson, Tamar Tenne, Ifaat Agmon-Fishman, Reut Tomashov Matar, Lina Basel-Salmon, Rivka Sukenik-Halevy. J Clin Med 2020
0

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

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