A citation-based method for searching scientific literature

Ron Hochstenbach, Ellen van Binsbergen, John Engelen, Aggie Nieuwint, Abeltje Polstra, Pino Poddighe, Claudia Ruivenkamp, Birgit Sikkema-Raddatz, Dominique Smeets, Martin Poot. Eur J Med Genet 2009
Times Cited: 124



Anita Rauch, Juliane Hoyer, Sabine Guth, Christiane Zweier, Cornelia Kraus, Christian Becker, Martin Zenker, Ulrike Hüffmeier, Christian Thiel, Franz Rüschendorf, Peter Nürnberg, André Reis, Udo Trautmann. Am J Med Genet A 2006
Times Cited: 224




List of shared articles



Times cited


Challenges in molecular diagnosis of X-linked Intellectual disability.
Chiara De Luca, Valérie Race, Liesbeth Keldermans, Marijke Bauters, Hilde Van Esch. Br Med Bull 2020
3

Array-CGH increased the diagnostic rate of developmental delay or intellectual disability in Taiwan.
Chung-Lin Lee, Chen-Hao Lee, Chih-Kuang Chuang, Huei-Ching Chiu, Yen-Jiun Chen, Chao-Ling Chou, Peih-Shan Wu, Chih-Ping Chen, Hsiang-Yu Lin, Shuan-Pei Lin. Pediatr Neonatol 2019
2

Personalized genome sequencing coupled with iPSC technology identifies GTDC1 as a gene involved in neurodevelopmental disorders.
Irene Aksoy, Kagistia H Utami, Cecilia L Winata, Axel M Hillmer, Sigrid L Rouam, Sylvain Briault, Sonia Davila, Lawrence W Stanton, Valere Cacheux. Hum Mol Genet 2017
6

Copy number variation analysis of patients with intellectual disability from North-West Spain.
Inés Quintela, Jesús Eirís, Carmen Gómez-Lado, Laura Pérez-Gay, David Dacruz, Raquel Cruz, Manuel Castro-Gago, Luz Míguez, Ángel Carracedo, Francisco Barros. Gene 2017
11

Array-CGH analysis in patients with intellectual disability and/or congenital malformations in Brazil.
G S Vianna, P F V Medeiros, A F Alves, T O Silva, F S Jehee. Genet Mol Res 2016
7

Genetic Approach to Diagnosis of Intellectual Disability.
Ratna Dua Puri, Moni Tuteja, I C Verma. Indian J Pediatr 2016
7

Chromosomal microarrays testing in children with developmental disabilities and congenital anomalies.
Guillermo Lay-Son, Karena Espinoza, Cecilia Vial, Juan C Rivera, María L Guzmán, Gabriela M Repetto. J Pediatr (Rio J) 2015
6

Chromosomal microarray impacts clinical management.
E R Riggs, K E Wain, D Riethmaier, B Smith-Packard, W A Faucett, N Hoppman, E C Thorland, V C Patel, D T Miller. Clin Genet 2014
51


Detection of chromosomal breakpoints in patients with developmental delay and speech disorders.
Kagistia H Utami, Axel M Hillmer, Irene Aksoy, Elaine G Y Chew, Audrey S M Teo, Zhenshui Zhang, Charlie W H Lee, Pauline J Chen, Chan Chee Seng, Pramila N Ariyaratne,[...]. PLoS One 2014
25

Performance of chromosomal microarray for patients with intellectual disabilities/developmental delay, autism, and multiple congenital anomalies in a Chinese cohort.
Wilson Wai Sing Chong, Ivan Fai Man Lo, Stephen Tak Sum Lam, Chi Chiu Wang, Ho Ming Luk, Tak Yeung Leung, Kwong Wai Choy. Mol Cytogenet 2014
26

Genetic basis of intellectual disability.
Jay W Ellison, Jill A Rosenfeld, Lisa G Shaffer. Annu Rev Med 2013
59

Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities.
Francesco Fiorentino, Stefania Napoletano, Fiorina Caiazzo, Mariateresa Sessa, Sara Bono, Letizia Spizzichino, Anthony Gordon, Andrea Nuccitelli, Giuseppe Rizzo, Marina Baldi. Eur J Hum Genet 2013
61

Clinical significance of de novo and inherited copy-number variation.
Anneke T Vulto-van Silfhout, Jayne Y Hehir-Kwa, Bregje W M van Bon, Janneke H M Schuurs-Hoeijmakers, Stephen Meader, Claudia J M Hellebrekers, Ilse J M Thoonen, Arjan P M de Brouwer, Han G Brunner, Caleb Webber,[...]. Hum Mutat 2013
73

Structural genomic variation in intellectual disability.
Rolph Pfundt, Joris A Veltman. Methods Mol Biol 2012
9

[Diagnostic investigations for an unexplained developmental disability].
A Verloes, D Héron, T Billette de Villemeur, A Afenjar, C Baumann, N Bahi-Buisson, P Charles, A Faudet, A Jacquette, C Mignot,[...]. Arch Pediatr 2012
6

Diagnostic exome sequencing in persons with severe intellectual disability.
Joep de Ligt, Marjolein H Willemsen, Bregje W M van Bon, Tjitske Kleefstra, Helger G Yntema, Thessa Kroes, Anneke T Vulto-van Silfhout, David A Koolen, Petra de Vries, Christian Gilissen,[...]. N Engl J Med 2012
961


A parallel SNP array study of genomic aberrations associated with mental retardation in patients and general population in Estonia.
Katrin Männik, Sven Parkel, Priit Palta, Olga Zilina, Helen Puusepp, Tõnu Esko, Reedik Mägi, Margit Nõukas, Andres Veidenberg, Mari Nelis,[...]. Eur J Med Genet 2011
6

Using a combination of MLPA kits to detect chromosomal imbalances in patients with multiple congenital anomalies and mental retardation is a valuable choice for developing countries.
Fernanda Sarquis Jehee, Jean Tetsuo Takamori, Paula F Vasconcelos Medeiros, Ana Carolina B Pordeus, Flavia Roche M Latini, Débora Romeo Bertola, Chong Ae Kim, Maria Rita Passos-Bueno. Eur J Med Genet 2011
31