A citation-based method for searching scientific literature

Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
Times Cited: 513

Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector, Karl Voelkerding, Heidi L Rehm. Genet Med 2015
Times Cited: 9176

List of shared articles

Times cited

Absence of heterozygosity detected by single-nucleotide polymorphism array in prenatal diagnosis.
J Liu, Z He, S Lin, Y Wang, L Huang, X Huang, Y Luo. Ultrasound Obstet Gynecol 2021

Improved molecular detection of mosaicism in Beckwith-Wiedemann Syndrome.
Samuel W Baker, Kelly A Duffy, Jennifer Richards-Yutz, Matthew A Deardorff, Jennifer M Kalish, Arupa Ganguly. J Med Genet 2021

A study of normal copy number variations in Israeli population.
Idit Maya, Pola Smirin-Yosef, Sarit Kahana, Sne Morag, Shiri Yacobson, Ifaat Agmon-Fishman, Reut Matar, Elisheva Bitton, Mordechai Shohat, Lina Basel-Salmon,[...]. Hum Genet 2021

Diagnostic yield of additional exome sequencing after the detection of long continuous stretches of homozygosity (LCSH) in SNP arrays.
Yanjie Fan, Lili Wang, Yu Sun, Ting Xu, Zhuwen Gong, Qianfeng Zhao, Wenjuan Qiu, Lili Liang, Bing Xiao, Huiwen Zhang,[...]. J Hum Genet 2021

Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype.
Farah Qaiser, Yue Yin, Carolyn B Mervis, Colleen A Morris, Bonita P Klein-Tasman, Elaine Tam, Lucy R Osborne, Ryan K C Yuen. Orphanet J Rare Dis 2021

Preimplantation genetic testing (PGT) for copy number variants of uncertain significance (CNV- VUS) in the genomic era: to do or not to do?
Keren Rotshenker-Olshinka, Naama Srebnik Moshe, Omri Weiss, Shira Shaviv, Orit Freireich, Reeval Segel, Sharon Zeligson, Talia Eldar-Geva, Gheona Altarescu. J Assist Reprod Genet 2021

ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data.
Andre E Minoche, Ben Lundie, Greg B Peters, Thomas Ohnesorg, Mark Pinese, David M Thomas, Andreas Zankl, Tony Roscioli, Nicole Schonrock, Sarah Kummerfeld,[...]. Genome Med 2021

Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.
Xiaofang Ding, Han Huang, Lili Zhong, Min Chen, Fang Peng, Bing Zhang, Xinyu Cui, Xiu-An Yang. Front Cell Infect Microbiol 2021

Prenatal Genetic Diagnosis in Three Fetuses With Left Heart Hypoplasia (LHH) From Three Unrelated Families.
Sukun Luo, Luyi Chen, Weizhong Wei, Li Tan, Meng Zhang, Zhengrong Duan, Jiangxia Cao, Yan Zhou, Aifen Zhou, Xuelian He. Front Cardiovasc Med 2021

The genetic landscape of intellectual disability and epilepsy in adults and the elderly: a systematic genetic work-up of 150 individuals.
Pia Zacher, Thomas Mayer, Frank Brandhoff, Tobias Bartolomaeus, Diana Le Duc, Martin Finzel, Anja Heinze, Susanne Horn, Chiara Klöckner, Gudrun Körber,[...]. Genet Med 2021

Next generation sequencing in children with unexplained epilepsy: A retrospective cohort study.
Wenjie Chen, Jiong Qin, Yiping Shen, Jingjing Liang, Yanan Cui, Ying Zhang. Brain Dev 2021