A citation-based method for searching scientific literature

Bradley P Coe, Kali Witherspoon, Jill A Rosenfeld, Bregje W M van Bon, Anneke T Vulto-van Silfhout, Paolo Bosco, Kathryn L Friend, Carl Baker, Serafino Buono, Lisenka E L M Vissers, Janneke H Schuurs-Hoeijmakers, Alex Hoischen, Rolph Pfundt, Nik Krumm, Gemma L Carvill, Deana Li, David Amaral, Natasha Brown, Paul J Lockhart, Ingrid E Scheffer, Antonino Alberti, Marie Shaw, Rosa Pettinato, Raymond Tervo, Nicole de Leeuw, Margot R F Reijnders, Beth S Torchia, Hilde Peeters, Brian J O'Roak, Marco Fichera, Jayne Y Hehir-Kwa, Jay Shendure, Heather C Mefford, Eric Haan, Jozef Gécz, Bert B A de Vries, Corrado Romano, Evan E Eichler. Nat Genet 2014
Times Cited: 313



Erin Rooney Riggs, Erica F Andersen, Athena M Cherry, Sibel Kantarci, Hutton Kearney, Ankita Patel, Gordana Raca, Deborah I Ritter, Sarah T South, Erik C Thorland, Daniel Pineda-Alvarez, Swaroop Aradhya, Christa Lese Martin. Genet Med 2020
Times Cited: 117




List of shared articles



Times cited

Universal chromosomal microarray analysis reveals high proportion of copy-number variants in low-risk pregnancies.
S Stern, N Hacohen, V Meiner, S Yagel, S Zenvirt, S Shkedi-Rafid, M Macarov, D V Valsky, S Porat, N Yanai,[...]. Ultrasound Obstet Gynecol 2021
6

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

CNV profiles of Chinese pediatric patients with developmental disorders.
Haiming Yuan, Shaofang Shangguan, Zhengchang Li, Jingsi Luo, Jiasun Su, Ruen Yao, Shun Zhang, Chen Liang, Qian Chen, Zhijie Gao,[...]. Genet Med 2021
1

Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability.
Guillaume Huguet, Catherine Schramm, Elise Douard, Petra Tamer, Antoine Main, Pauline Monin, Jade England, Khadije Jizi, Thomas Renne, Myriam Poirier,[...]. Mol Psychiatry 2021
3

Usefulness of copy number variant detection following monogenic disease exclusion in prenatal diagnosis.
Panlai Shi, Yanjie Xia, Qianqian Li, Xiangdong Kong. J Obstet Gynaecol Res 2021
0

Long-read genome sequencing for the molecular diagnosis of neurodevelopmental disorders.
Susan M Hiatt, James M J Lawlor, Lori H Handley, Ryne C Ramaker, Brianne B Rogers, E Christopher Partridge, Lori Beth Boston, Melissa Williams, Christopher B Plott, Jerry Jenkins,[...]. HGG Adv 2021
0

Estimating the effects of copy-number variants on intelligence using hierarchical Bayesian models.
Lai Jiang, Guillaume Huguet, Catherine Schramm, Antonio Ciampi, Antoine Main, Claudine Passo, Martineau Jean-Louis, Maude Auger, Gunter Schumann, David Porteous,[...]. Genet Epidemiol 2020
0

Haploinsufficiency of ATP6V0C possibly underlies 16p13.3 deletions that cause microcephaly, seizures, and neurodevelopmental disorder.
Rory J Tinker, George J Burghel, Shruti Garg, Maggie Steggall, Sara Cuvertino, Siddharth Banka. Am J Med Genet A 2020
0

Copy number variation (CNV) identification, interpretation, and database from Brazilian patients.
Victória Cabral Silveira Monteiro de Godoy, Fernanda Teixeira Bellucco, Mileny Colovati, Hélio Rodrigues de Oliveira-Junior, Mariana Moysés-Oliveira, Maria Isabel Melaragno. Genet Mol Biol 2020
0