A citation-based method for searching scientific literature

Jill A Rosenfeld, Bradley P Coe, Evan E Eichler, Howard Cuckle, Lisa G Shaffer. Genet Med 2013
Times Cited: 174



Evangelos Vassos, David A Collier, Simon Holden, Christine Patch, Dan Rujescu, David St Clair, Cathryn M Lewis. Hum Mol Genet 2010
Times Cited: 104




List of shared articles



Times cited

Genomic Variation, Evolvability, and the Paradox of Mental Illness.
Camillo Thomas Gualtieri. Front Psychiatry 2021
0

Clinical characterization of individuals with the distal 1q21.1 microdeletion.
Stacey D Edwards, Katharina V Schulze, Jill A Rosenfeld, Lauren E Westerfield, Amanda Gerard, Bo Yuan, Elena L Grigorenko, Jennifer E Posey, Weimin Bi, Pengfei Liu. Am J Med Genet A 2021
0

CalPen (Calculator of Penetrance), a web-based tool to estimate penetrance in complex genetic disorders.
Aditya Addepalli, Sakhare Kalyani, Minali Singh, Debashree Bandyopadhyay, K Naga Mohan. PLoS One 2020
2

NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families.
Maryam Al Shehhi, Eva B Forman, Jacqueline E Fitzgerald, Veronica McInerney, Janusz Krawczyk, Sanbing Shen, David R Betts, Linda Mc Ardle, Kathleen M Gorman, Mary D King,[...]. Eur J Med Genet 2019
22

Phenotypic association of 15q11.2 CNVs of the region of breakpoints 1-2 (BP1-BP2) in a large cohort of samples referred for genetic diagnosis.
K Naga Mohan, Ye Cao, Justin Pham, Sau Wai Cheung, Lori Hoffner, Z Zishuo Ou, Urvashi Surti, Edwin H Cook, Arthur L Beaudet. J Hum Genet 2019
6

When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations.
Idit Maya, Reuven Sharony, Shiri Yacobson, Sarit Kahana, Josepha Yeshaya, Tamar Tenne, Ifaat Agmon-Fishman, Lital Cohen-Vig, Yael Goldberg, Racheli Berger,[...]. Genet Med 2018
24

Bayesian approach to determining penetrance of pathogenic SDH variants.
Diana E Benn, Ying Zhu, Katrina A Andrews, Mathilda Wilding, Emma L Duncan, Trisha Dwight, Richard W Tothill, John Burgess, Ashley Crook, Anthony J Gill,[...]. J Med Genet 2018
17