A citation-based method for searching scientific literature

Reza Asadollahi, Beatrice Oneda, Pascal Joset, Silvia Azzarello-Burri, Deborah Bartholdi, Katharina Steindl, Marie Vincent, Joana Cobilanschi, Heinrich Sticht, Rosa Baldinger, Regina Reissmann, Irene Sudholt, Christian T Thiel, Arif B Ekici, André Reis, Emilia K Bijlsma, Joris Andrieux, Anne Dieux, David FitzPatrick, Susanne Ritter, Alessandra Baumer, Beatrice Latal, Barbara Plecko, Oskar G Jenni, Anita Rauch. J Med Genet 2014
Times Cited: 57



David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein, W Andrew Faucett, Lars Feuk, Jan M Friedman, Ada Hamosh, Laird Jackson, Erin B Kaminsky, Klaas Kok, Ian D Krantz, Robert M Kuhn, Charles Lee, James M Ostell, Carla Rosenberg, Stephen W Scherer, Nancy B Spinner, Dimitri J Stavropoulos, James H Tepperberg, Erik C Thorland, Joris R Vermeesch, Darrel J Waggoner, Michael S Watson, Christa Lese Martin, David H Ledbetter. Am J Hum Genet 2010
Times Cited: 1511




List of shared articles



Times cited

ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data.
Andre E Minoche, Ben Lundie, Greg B Peters, Thomas Ohnesorg, Mark Pinese, David M Thomas, Andreas Zankl, Tony Roscioli, Nicole Schonrock, Sarah Kummerfeld,[...]. Genome Med 2021
5

CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens.
Binbin Wang, Taoyun Ji, Xueya Zhou, Jing Wang, Xi Wang, Jingmin Wang, Dingliang Zhu, Xuejun Zhang, Pak Chung Sham, Xuegong Zhang,[...]. Sci Rep 2016
9

5p deletions: Current knowledge and future directions.
Joanne M Nguyen, Krista J Qualmann, Rebecca Okashah, AmySue Reilly, Mikhail F Alexeyev, Dennis J Campbell. Am J Med Genet C Semin Med Genet 2015
38


The Cytoscan HD Array in the Diagnosis of Neurodevelopmental Disorders.
Francesca Scionti, Maria Teresa Di Martino, Licia Pensabene, Valentina Bruni, Daniela Concolino. High Throughput 2018
1

Challenges in the clinical interpretation of small de novo copy number variants in neurodevelopmental disorders.
Pamela Magini, Emanuela Scarano, Ilaria Donati, Alberto Sensi, Laura Mazzanti, Annamaria Perri, Federica Tamburrino, Patrizia Mongelli, Antonio Percesepe, Paola Visconti,[...]. Gene 2019
4

Attention Deficit Hyperactivity and Autism Spectrum Disorders as the Core Symptoms of AUTS2 Syndrome: Description of Five New Patients and Update of the Frequency of Manifestations and Genotype-Phenotype Correlation.
Carolina Sanchez-Jimeno, Fiona Blanco-Kelly, Fermina López-Grondona, Rebeca Losada-Del Pozo, Beatriz Moreno, María Rodrigo-Moreno, Elena Martinez-Cayuelas, Rosa Riveiro-Alvarez, María Fenollar-Cortés, Carmen Ayuso,[...]. Genes (Basel) 2021
0

Application of high-resolution array platform for genome-wide copy number variation analysis in patients with nonsyndromic cleft lip and palate.
Heglayne Pereira Vital da Silva, Gustavo Henrique de Medeiros Oliveira, Marcela Abbott Galvão Ururahy, João Felipe Bezerra, Karla Simone Costa de Souza, Raul Hernandes Bortolin, André Ducati Luchessi, Vivian Nogueira Silbiger, Valéria Morgiana Gualberto Duarte Moreira Lima, Gisele Correia Pacheco Leite,[...]. J Clin Lab Anal 2018
6

Clinical relevance of small copy-number variants in chromosomal microarray clinical testing.
Dana Hollenbeck, Crescenda L Williams, Kathryn Drazba, Maria Descartes, Bruce R Korf, S Lane Rutledge, Edward J Lose, Nathaniel H Robin, Andrew J Carroll, Fady M Mikhail. Genet Med 2017
12

Elucidation of the phenotypic spectrum and genetic landscape in primary and secondary microcephaly.
Paranchai Boonsawat, Pascal Joset, Katharina Steindl, Beatrice Oneda, Laura Gogoll, Silvia Azzarello-Burri, Frenny Sheth, Chaitanya Datar, Ishwar C Verma, Ratna Dua Puri,[...]. Genet Med 2019
22