A citation-based method for searching scientific literature

Jill A Rosenfeld, Bradley P Coe, Evan E Eichler, Howard Cuckle, Lisa G Shaffer. Genet Med 2013
Times Cited: 181



Olivier Vanakker, Catheline Vilain, Katrien Janssens, Nathalie Van der Aa, Guillaume Smits, Claude Bandelier, Bettina Blaumeiser, Saskia Bulk, Jean-Hubert Caberg, Anne De Leener, Marjan De Rademaeker, Thomy de Ravel, Julie Desir, Anne Destree, Annelies Dheedene, Stéphane Gaillez, Bernard Grisart, Ann-Cécile Hellin, Sandra Janssens, Kathelijn Keymolen, Björn Menten, Bruno Pichon, Marie Ravoet, Nicole Revencu, Sonia Rombout, Catherine Staessens, Ann Van Den Bogaert, Kris Van Den Bogaert, Joris R Vermeesch, Frank Kooy, Yves Sznajer, Koen Devriendt. Eur J Med Genet 2014
Times Cited: 56




List of shared articles



Times cited

Is fetal isolated double renal collecting system an indication for chromosomal microarray?
Amihood Singer, Idit Maya, Ayala Frumkin, Sharon Zeligson, Sagi Ben Yehoshua Josefsberg, Racheli Berger, Shay Ben Shachar, Lena Sagi-Dain. J Matern Fetal Neonatal Med 2021
1

What is the meaning of a 'genomic result' in the context of pregnancy?
Shiri Shkedi-Rafid, Rachel Horton, Anneke Lucassen. Eur J Hum Genet 2021
0

Prenatal chromosome microarray: 'The UK experience'. A survey of reporting practices in UK genetic services (2012-2019).
Jenny Patterson, Diana Wellesley, Sian Morgan, Deirdre Cilliers, Stephanie Allen, Carol A Gardiner. Prenat Diagn 2021
0

Prenatally detected copy number variants in a national cohort: A postnatal follow-up study.
Joke Muys, Yves Jacquemyn, Bettina Blaumeiser, Laura Bourlard, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Anne De Leener, Marjan De Rademaeker, Julie Désir,[...]. Prenat Diagn 2020
1

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

Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada.
Christine M Armour, Shelley Danielle Dougan, Jo-Ann Brock, Radha Chari, Bernie N Chodirker, Isabelle DeBie, Jane A Evans, William T Gibson, Elena Kolomietz, Tanya N Nelson,[...]. J Med Genet 2018
25


The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations.
Joke Muys, Bettina Blaumeiser, Yves Jacquemyn, Claude Bandelier, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Winnie Courtens, Anne De Leener, Marjan De Rademaeker,[...]. Prenat Diagn 2018
14

Microarrays in prenatal diagnosis.
Beatrice Oneda, Anita Rauch. Best Pract Res Clin Obstet Gynaecol 2017
20

Recommendations for the use of microarrays in prenatal diagnosis.
Javier Suela, Isabel López-Expósito, María Eugenia Querejeta, Rosa Martorell, Esther Cuatrecasas, Lluis Armengol, Eugenia Antolín, Elena Domínguez Garrido, María José Trujillo-Tiebas, Jordi Rosell,[...]. Med Clin (Barc) 2017
4