A citation-based method for searching scientific literature

Kai Wang, Mingyao Li, Dexter Hadley, Rui Liu, Joseph Glessner, Struan F A Grant, Hakon Hakonarson, Maja Bucan. Genome Res 2007
Times Cited: 1148



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

Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants.
Elmo Christian Saarentaus, Aki Samuli Havulinna, Nina Mars, Ari Ahola-Olli, Tuomo Tapio Johannes Kiiskinen, Juulia Partanen, Sanni Ruotsalainen, Mitja Kurki, Lea Martta Urpa, Lei Chen,[...]. Mol Psychiatry 2021
0

Genome-wide copy number variations in a large cohort of bantu African children.
Feyza Yilmaz, Megan Null, David Astling, Hung-Chun Yu, Joanne Cole, Stephanie A Santorico, Benedikt Hallgrimsson, Mange Manyama, Richard A Spritz, Audrey E Hendricks,[...]. BMC Med Genomics 2021
0

Detection of copy number variants in African goats using whole genome sequence data.
Wilson Nandolo, Gábor Mészáros, Maria Wurzinger, Liveness J Banda, Timothy N Gondwe, Henry A Mulindwa, Helen N Nakimbugwe, Emily L Clark, M Jennifer Woodward-Greene, Mei Liu,[...]. BMC Genomics 2021
0

Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents.
Dinka Smajlagić, Ksenia Lavrichenko, Siren Berland, Øyvind Helgeland, Gun Peggy Knudsen, Marc Vaudel, Jan Haavik, Per Morten Knappskog, Pål Rasmus Njølstad, Gunnar Houge,[...]. Eur J Hum Genet 2021
3

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.
Dennis van der Meer, Ida E Sønderby, Tobias Kaufmann, G Bragi Walters, Abdel Abdellaoui, David Ames, Katrin Amunts, Micael Andersson, Nicola J Armstrong, Manon Bernard,[...]. JAMA Psychiatry 2020
19

Copy Number Variation and Clinical Outcomes in Patients With Germline PTEN Mutations.
Lamis Yehia, Marilyn Seyfi, Lisa-Marie Niestroj, Roshan Padmanabhan, Ying Ni, Thomas W Frazier, Dennis Lal, Charis Eng. JAMA Netw Open 2020
2

Sensitivity to gene dosage and gene expression affects genes with copy number variants observed among neuropsychiatric diseases.
Maria Yamasaki, Takashi Makino, Seik-Soon Khor, Hiromi Toyoda, Taku Miyagawa, Xiaoxi Liu, Hitoshi Kuwabara, Yukiko Kano, Takafumi Shimada, Toshiro Sugiyama,[...]. BMC Med Genomics 2020
2

Large Copy-Number Variants in UK Biobank Caused by Clonal Hematopoiesis May Confound Penetrance Estimates.
Marcus Tuke, Jessica Tyrrell, Katherine S Ruth, Robin N Beaumont, Andrew R Wood, Anna Murray, Timothy M Frayling, Michael N Weedon, Caroline F Wright. Am J Hum Genet 2020
1


Contribution of de novo and inherited rare CNVs to very preterm birth.
Hilary S Wong, Megan Wadon, Alexandra Evans, George Kirov, Neena Modi, Michael C O'Donovan, Anita Thapar. J Med Genet 2020
1