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







List of shared articles



Times cited

Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG).
Kandamurugu Manickam, Monica R McClain, Laurie A Demmer, Sawona Biswas, Hutton M Kearney, Jennifer Malinowski, Lauren J Massingham, Danny Miller, Timothy W Yu, Fuki M Hisama. Genet Med 2021
0


Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability.
Jennifer Malinowski, David T Miller, Laurie Demmer, Jennifer Gannon, Elaine Maria Pereira, Molly C Schroeder, Maren T Scheuner, Anne Chun-Hui Tsai, Scott E Hickey, Jun Shen. Genet Med 2020
14

Chromosomal Microarray Analysis in Turkish Patients with Unexplained Developmental Delay and Intellectual Developmental Disorders.
Hakan Gürkan, Emine İkbal Atli, Engin Atli, Leyla Bozatli, Mengühan Araz Altay, Sinem Yalçintepe, Yasemin Özen, Damla Eker, Çisem Akurut, Selma Demır,[...]. Noro Psikiyatr Ars 2020
0

Application of chromosome microarray analysis in patients with unexplained developmental delay/intellectual disability in South China.
Rongyue Wang, Tingying Lei, Fang Fu, Ru Li, Xiangyi Jing, Xin Yang, Juan Liu, Dongzhi Li, Can Liao. Pediatr Neonatol 2019
9

The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay.
Marketa Wayhelova, Jan Smetana, Vladimira Vallova, Eva Hladilkova, Hana Filkova, Marta Hanakova, Marcela Vilemova, Petra Nikolova, Barbora Gromesova, Renata Gaillyova,[...]. BMC Med Genomics 2019
2


Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Darrel Waggoner, Karen E Wain, Adrian M Dubuc, Laura Conlin, Scott E Hickey, Allen N Lamb, Christa Lese Martin, Cynthia C Morton, Kristen Rasmussen, Jane L Schuette,[...]. Genet Med 2018
17

A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability.
J R M Ceroni, R L Dutra, R S Honjo, J C Llerena, A X Acosta, P F V Medeiros, M F Galera, É A Zanardo, F B Piazzon, A T Dias,[...]. Sci Rep 2018
1


Cytogenomic assessment of the diagnosis of 93 patients with developmental delay and multiple congenital abnormalities: The Brazilian experience.
Évelin Aline Zanardo, Roberta Lelis Dutra, Flavia Balbo Piazzon, Alexandre Torchio Dias, Gil Monteiro Novo-Filho, Amom Mendes Nascimento, Marília Moreira Montenegro, Jullian Gabriel Damasceno, Fabrícia Andreia Rosa Madia, Thaís Virgínia Moura Machado da Costa,[...]. Clinics (Sao Paulo) 2017
7

Clinical performance of the CytoScan Dx Assay in diagnosing developmental delay/intellectual disability.
Rolph Pfundt, Kat Kwiatkowski, Alan Roter, Anju Shukla, Eric Thorland, Richard Hockett, Barbara DuPont, Eric T Fung, Alka Chaubey. Genet Med 2016
7

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

Recent advances of genomic testing in perinatal medicine.
David G Peters, Svetlana A Yatsenko, Urvashi Surti, Aleksandar Rajkovic. Semin Perinatol 2015
17

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

CNV-ROC: A cost effective, computer-aided analytical performance evaluator of chromosomal microarrays.
Corey W Goodman, Heather J Major, William D Walls, Val C Sheffield, Thomas L Casavant, Benjamin W Darbro. J Biomed Inform 2015
0

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

The clinical impact of chromosomal microarray on paediatric care in Hong Kong.
Victoria Q Tao, Kelvin Y K Chan, Yoyo W Y Chu, Gary T K Mok, Tiong Y Tan, Wanling Yang, So Lun Lee, Wing Fai Tang, Winnie W Y Tso, Elizabeth T Lau,[...]. PLoS One 2014
15

High resolution chromosomal microarray in undiagnosed neurological disorders.
Katherine B Howell, Andrew J Kornberg, A Simon Harvey, Monique M Ryan, Mark T Mackay, Jeremy L Freeman, M Victoria Rodriguez Casero, Kevin J Collins, Michael Hayman, Ahmad Mohamed,[...]. J Paediatr Child Health 2013
16

[Advances in the identification of the aetiology of mental retardation].
Gabriel González, Víctor Raggio, María Boidi, Alejandra Tapié, Leda Roche. Rev Neurol 2013
3

[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

Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing.
George McGillivray, Jill A Rosenfeld, R J McKinlay Gardner, Lynn H Gillam. Prenat Diagn 2012
68

Clinical utility of chromosomal microarray analysis.
Jay W Ellison, J Britt Ravnan, Jill A Rosenfeld, S Annie Morton, Nicholas J Neill, Marc S Williams, Jodi Lewis, Beth S Torchia, Cathryn Walker, Ryan N Traylor,[...]. Pediatrics 2012
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