A citation-based method for searching scientific literature

David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein, W Andrew Faucett, Lars Feuk, Jan M Friedman, Ada Hamosh, Laird Jackson, Erin B Kaminsky, Klaas Kok, Ian D Krantz, Robert M Kuhn, Charles Lee, James M Ostell, Carla Rosenberg, Stephen W Scherer, Nancy B Spinner, Dimitri J Stavropoulos, James H Tepperberg, Erik C Thorland, Joris R Vermeesch, Darrel J Waggoner, Michael S Watson, Christa Lese Martin, David H Ledbetter. Am J Hum Genet 2010
Times Cited: 1469



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: 637




List of shared articles



Times cited

Diagnostic and clinical utility of next-generation sequencing in children born with multiple congenital anomalies in the China neonatal genomes project.
Huijun Wang, Feifan Xiao, Xinran Dong, Yulan Lu, Guoqiang Cheng, Laishuan Wang, Wei Lu, Lin Yang, Liping Chen, Wenqing Kang,[...]. Hum Mutat 2021
0

Prenatal Diagnosis by Chromosome Microarray Analysis, An Indian Experience.
Meena Bajaj Lall, Shruti Agarwal, Preeti Paliwal, Pushpa Saviour, Anju Joshi, Arti Joshi, Surbhi Mahajan, Sunita Bijarnia-Mahay, Ratna Dua Puri, I C Verma. J Obstet Gynaecol India 2021
0

Performances of NIPT for copy number variations at different sequencing depths using the semiconductor sequencing platform.
Jiexia Yang, Jing Wu, Haishan Peng, Yaping Hou, Fangfang Guo, Dongmei Wang, Haoxin Ouyang, Yixia Wang, Aihua Yin. Hum Genomics 2021
0

Universal chromosomal microarray analysis reveals high proportion of copy-number variants in low-risk pregnancies.
S Stern, N Hacohen, V Meiner, S Yagel, S Zenvirt, S Shkedi-Rafid, M Macarov, D V Valsky, S Porat, N Yanai,[...]. Ultrasound Obstet Gynecol 2021
7

Prenatal chromosomal microarray analysis in 2466 fetuses with ultrasonographic soft markers: a prospective cohort study.
Ting Hu, Tian Tian, Zhu Zhang, Jiamin Wang, Rui Hu, Like Xiao, Hongmei Zhu, Yi Lai, He Wang, Shanling Liu. Am J Obstet Gynecol 2021
1

The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings.
Annie Sy Hui, Matthew Hoi Kin Chau, Yiu Man Chan, Ye Cao, Angel Hw Kwan, Xiaofan Zhu, Yvonne K Kwok, Zihan Chen, Terence T Lao, Kwong Wai Choy,[...]. Acta Obstet Gynecol Scand 2021
1

Cell-free DNA analysis of maternal blood in prenatal screening for chromosomal microdeletions and microduplications: a systematic review.
Alessandra Familiari, Simona Boito, Georgios Rembouskos, Benedetta Ischia, Veronica Accurti, Isabella Fabietti, Paolo Volpe, Nicola Persico. Prenat Diagn 2021
0

Cytogenetic and molecular diagnostic testing associated with prenatal and postnatal birth defects.
Stela Z Berisha, Shashi Shetty, Thomas W Prior, Anna L Mitchell. Birth Defects Res 2020
1