A citation-based method for searching scientific literature

Sarah T South, Charles Lee, Allen N Lamb, Anne W Higgins, Hutton M Kearney. Genet Med 2013
Times Cited: 159



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: 799




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


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
6

New Insights into the Impact of Genome-Wide Copy Number Variations on Complex Congenital Heart Disease in Saudi Arabia.
Majed J Dasouki, Salma M Wakil, Olfat Al-Harazi, Maarab Alkorashy, Nzioka P Muiya, Editha Andres, Samya Hagos, Haya Aldusery, Nduna Dzimiri, Dilek Colak. OMICS 2020
1

The copy number variation landscape of congenital anomalies of the kidney and urinary tract.
Miguel Verbitsky, Rik Westland, Alejandra Perez, Krzysztof Kiryluk, Qingxue Liu, Priya Krithivasan, Adele Mitrotti, David A Fasel, Ekaterina Batourina, Matthew G Sampson,[...]. Nat Genet 2019
44

Are all chromosome microarrays the same? What clinicians need to know.
Brynn Levy, Rachel D Burnside. Prenat Diagn 2019
8


Structural variation at the CYP2C locus: Characterization of deletion and duplication alleles.
Mariana R Botton, Xingwu Lu, Geping Zhao, Elena Repnikova, Yoshinori Seki, Andrea Gaedigk, Eric E Schadt, Lisa Edelmann, Stuart A Scott. Hum Mutat 2019
4

Subchromosomal anomalies in small for gestational-age fetuses and newborns.
Ying Ma, Yan Pei, Chenghong Yin, Yuxin Jiang, Jingjing Wang, Xiaofei Li, Lin Li, Karl Oliver Kagan, Qingqing Wu. Arch Gynecol Obstet 2019
2

Genetic basis of human congenital anomalies of the kidney and urinary tract.
Simone Sanna-Cherchi, Rik Westland, Gian Marco Ghiggeri, Ali G Gharavi. J Clin Invest 2018
32