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



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: 8923




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
0

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
1

Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia.
Bahareh A Mojarad, Yue Yin, Roozbeh Manshaei, Ian Backstrom, Gregory Costain, Tracy Heung, Daniele Merico, Christian R Marshall, Anne S Bassett, Ryan K C Yuen. Transl Psychiatry 2021
0

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
2

Genetic Testing in Neurodevelopmental Disorders.
Juliann M Savatt, Scott M Myers. Front Pediatr 2021
3

Investigation on combined copy number variation sequencing and cytogenetic karyotyping for prenatal diagnosis.
Jinman Zhang, Xinhua Tang, Jilin Hu, Guilin He, Jian Wang, Yingting Zhu, Baosheng Zhu. BMC Pregnancy Childbirth 2021
0

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
0

Genetic diagnoses in pediatric patients with epilepsy and comorbid intellectual disability.
Mei Yang, Bocheng Xu, Jiamin Wang, Zhu Zhang, Hanbing Xie, He Wang, Ting Hu, Shanling Liu. Epilepsy Res 2021
0

Chromosomal microarray detects genetic risks of neurodevelopmental disorders in newborns with congenital heart disease.
Kamalvir Gill, Jun Sasaki, Parul Jayakar, Lisa Sosa, Elizabeth Welch. Cardiol Young 2021
0

Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders.
Bekim Sadikovic, Michael A Levy, Jennifer Kerkhof, Erfan Aref-Eshghi, Laila Schenkel, Alan Stuart, Haley McConkey, Peter Henneman, Andrea Venema, Charles E Schwartz,[...]. Genet Med 2021
0

PLXNA2 and LRRC40 as candidate genes in autism spectrum disorder.
Jordi Pijuan, Juan Darío Ortigoza-Escobar, Juan Ortiz, Adrián Alcalá, María José Calvo, Mariona Cubells, Cristina Hernando-Davalillo, Francesc Palau, Janet Hoenicka. Autism Res 2021
1

Guidelines for genetic testing of muscle and neuromuscular junction disorders.
Stefan Nicolau, Margherita Milone, Teerin Liewluck. Muscle Nerve 2021
0