A citation-based method for searching scientific literature

Cornelis A Albers, Dirk S Paul, Harald Schulze, Kathleen Freson, Jonathan C Stephens, Peter A Smethurst, Jennifer D Jolley, Ana Cvejic, Myrto Kostadima, Paul Bertone, Martijn H Breuning, Najet Debili, Panos Deloukas, Rémi Favier, Janine Fiedler, Catherine M Hobbs, Ni Huang, Matthew E Hurles, Graham Kiddle, Ingrid Krapels, Paquita Nurden, Claudia A L Ruivenkamp, Jennifer G Sambrook, Kenneth Smith, Derek L Stemple, Gabriele Strauss, Chantal Thys, Chris van Geet, Ruth Newbury-Ecob, Willem H Ouwehand, Cedric Ghevaert. Nat Genet 2012
Times Cited: 251



Jill A Rosenfeld, Ryan N Traylor, G Bradley Schaefer, Elizabeth W McPherson, Blake C Ballif, Eva Klopocki, Stefan Mundlos, Lisa G Shaffer, Arthur S Aylsworth. Eur J Hum Genet 2012
Times Cited: 61




List of shared articles



Times cited

Is fetal isolated double renal collecting system an indication for chromosomal microarray?
Amihood Singer, Idit Maya, Ayala Frumkin, Sharon Zeligson, Sagi Ben Yehoshua Josefsberg, Racheli Berger, Shay Ben Shachar, Lena Sagi-Dain. J Matern Fetal Neonatal Med 2021
1

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


Discordance of cardiovascular abnormalities in a monozygotic twin pair carrying a class II 1q21.1 microdeletion.
Shan-Shan Shi, Shao-Bin Lin, Dan-Lei Cai, Wang-Rong Wen, Rui-Man Li. Taiwan J Obstet Gynecol 2020
1

Identifying chromosomal subpopulations based on their recombination histories advances the study of the genetic basis of phenotypic traits.
Carlos Ruiz-Arenas, Alejandro Cáceres, Marcos López, Dolors Pelegrí-Sisó, Josefa González, Juan R González. Genome Res 2020
0

The role of p53 in developmental syndromes.
Margot E Bowen, Laura D Attardi. J Mol Cell Biol 2019
15

The stability of Magoh and Y14 depends on their heterodimer formation and nuclear localization.
Qingfeng Ma, Takanori Tatsuno, Yuka Nakamura, Yasuhito Ishigaki. Biochem Biophys Res Commun 2019
2

1q21.1 deletion and a rare functional polymorphism in siblings with thrombocytopenia-absent radius-like phenotypes.
Seth A Brodie, Jean Paul Rodriguez-Aulet, Neelam Giri, Jieqiong Dai, Mia Steinberg, Joshua J Waterfall, David Roberson, Bari J Ballew, Weiyin Zhou, Sarah L Anzick,[...]. Cold Spring Harb Mol Case Stud 2019
0


The exon junction complex: a lifelong guardian of mRNA fate.
Lauren A Woodward, Justin W Mabin, Pooja Gangras, Guramrit Singh. Wiley Interdiscip Rev RNA 2017
38