A citation-based method for searching scientific literature

Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig, Hoda Abdel-Hamid, Patricia Bader, Elizabeth McCracken, Dmitriy Niyazov, Kathleen Leppig, Heidi Thiese, Marybeth Hummel, Nora Alexander, Jerome Gorski, Jennifer Kussmann, Vandana Shashi, Krys Johnson, Catherine Rehder, Blake C Ballif, Lisa G Shaffer, Evan E Eichler. Nat Genet 2011
Times Cited: 778



Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman, Susan Klugman, Thomas Scholl, Joe Leigh Simpson, Kimberly McCall, Vimla S Aggarwal, Brian Bunke, Odelia Nahum, Ankita Patel, Allen N Lamb, Elizabeth A Thom, Arthur L Beaudet, David H Ledbetter, Lisa G Shaffer, Laird Jackson. N Engl J Med 2012
Times Cited: 597




List of shared articles



Times cited

Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.
Miguel Verbitsky, Priya Krithivasan, Ekaterina Batourina, Atlas Khan, Sarah E Graham, Maddalena Marasà, Hyunwoo Kim, Tze Y Lim, Patricia L Weng, Elena Sánchez-Rodríguez,[...]. J Am Soc Nephrol 2021
0

Exploring copy number variants in deceased fetuses and neonates with abnormal vertebral patterns and cervical ribs.
Pauline C Schut, Erwin Brosens, Tom J M Van Dooren, Frietson Galis, Clara M A Ten Broek, Inge M M Baijens, Marjolein H G Dremmen, Dick Tibboel, Martin P Schol, Annelies de Klein,[...]. Birth Defects Res 2020
1

Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis.
Huilin Wang, Zirui Dong, Rui Zhang, Matthew Hoi Kin Chau, Zhenjun Yang, Kathy Yin Ching Tsang, Hoi Kin Wong, Baoheng Gui, Zhuo Meng, Kelin Xiao,[...]. Genet Med 2020
18

Chromosomal microarray analysis in prenatal diagnosis: ethical considerations of the Belgian approach.
Joke Muys, Bettina Blaumeiser, Katrien Janssens, Patrick Loobuyck, Yves Jacquemyn. J Med Ethics 2020
7

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020
254

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