A citation-based method for searching scientific literature

George Kirov, Elliott Rees, James T R Walters, Valentina Escott-Price, Lyudmila Georgieva, Alexander L Richards, Kimberly D Chambert, Gerwyn Davies, Sophie E Legge, Jennifer L Moran, Steven A McCarroll, Michael C O'Donovan, Michael J Owen. Biol Psychiatry 2014
Times Cited: 190



Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
Times Cited: 504




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

Chromosomal Microarray Analysis for the Prenatal Diagnosis in Fetuses with Nasal Bone Hypoplasia: A Retrospective Cohort Study.
Hailong Huang, Meiying Cai, Wei Ma, Na Lin, Liangpu Xu. Risk Manag Healthc Policy 2021
0

Role of late amniocentesis in the era of modern genomic technologies.
H Daum, A Ben David, M Nadjari, S Zenvirt, S Helman, N Yanai, V Meiner, S Yagel, A Frumkin, S Shkedi Rafid. Ultrasound Obstet Gynecol 2019
5

Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank.
Karen Crawford, Matthew Bracher-Smith, David Owen, Kimberley M Kendall, Elliott Rees, Antonio F Pardiñas, Mark Einon, Valentina Escott-Price, James T R Walters, Michael C O'Donovan,[...]. J Med Genet 2019
37

Rare copy number variants contribute pathogenic alleles in patients with intestinal malrotation.
Karin Salehi Karlslätt, Maria Pettersson, Nina Jäntti, Przemyslaw Szafranski, Tomas Wester, Britt Husberg, Ulla Ullberg, Pawel Stankiewicz, Ann Nordgren, Johanna Lundin,[...]. Mol Genet Genomic Med 2019
5

Experience of chromosomal microarray applied in prenatal and postnatal settings in Hong Kong.
Shirley S W Cheng, Kelvin Y K Chan, Kelphen K P Leung, Patrick K C Au, Wai-Keung Tam, Samuel K M Li, Ho-Ming Luk, Anita S Y Kan, Brian H Y Chung, Ivan F M Lo,[...]. Am J Med Genet C Semin Med Genet 2019
11

Estimating the effect size of the 15Q11.2 BP1-BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice.
Aia Elise Jønch, Elise Douard, Clara Moreau, Anke Van Dijck, Marzia Passeggeri, Frank Kooy, Jacques Puechberty, Carolyn Campbell, Damien Sanlaville, Henrietta Lefroy,[...]. J Med Genet 2019
13

Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders.
L D'Abate, S Walker, R K C Yuen, K Tammimies, J A Buchanan, R W Davies, B Thiruvahindrapuram, J Wei, J Brian, S E Bryson,[...]. Nat Commun 2019
9

Identification of putative second genetic hits in schizophrenia carriers of high-risk copy number variants and resequencing in additional samples.
Julio Rodríguez-López, Beatriz Sobrino, Jorge Amigo, Noa Carrera, Julio Brenlla, Santiago Agra, Eduardo Paz, Ángel Carracedo, Mario Páramo, Manuel Arrojo,[...]. Eur Arch Psychiatry Clin Neurosci 2018
2

Genome wide analysis of rare copy number variations in alcohol abuse or dependence.
Julio Rodríguez-López, Gerardo Flórez, Vanessa Blanco, César Pereiro, José Manuel Fernández, Emilio Fariñas, Valentín Estévez, Jesús Gómez-Trigo, Xaquín Gurriarán, Raquel Calvo,[...]. J Psychiatr Res 2018
5