A citation-based method for searching scientific literature

M Schmid, S Stary, S Springer, D Bettelheim, P Husslein, B Streubel. Ultrasound Obstet Gynecol 2013
Times Cited: 10







List of co-cited articles
92 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Array comparative genomic hybridization in prenatal diagnosis: another experience.
F Vialard, D Molina Gomes, B Leroy, E Quarello, A Escalona, C Le Sciellour, V Serazin, J Roume, Y Ville, P de Mazancourt,[...]. Fetal Diagn Ther 2009
58
20

Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations.
C Le Caignec, M Boceno, P Saugier-Veber, S Jacquemont, M Joubert, A David, T Frebourg, J M Rival. J Med Genet 2005
147
20

Ultrasonographically detectable markers of fetal chromosomal abnormalities.
K H Nicolaides, R J Snijders, C M Gosden, C Berry, S Campbell. Lancet 1992
212
20

Clinical diagnosis by whole-genome sequencing of a prenatal sample.
Michael E Talkowski, Zehra Ordulu, Vamsee Pillalamarri, Carol B Benson, Ian Blumenthal, Susan Connolly, Carrie Hanscom, Naveed Hussain, Shahrin Pereira, Jonathan Picker,[...]. N Engl J Med 2012
119
20

Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients.
M De Gregori, R Ciccone, P Magini, T Pramparo, S Gimelli, J Messa, F Novara, A Vetro, E Rossi, P Maraschio,[...]. J Med Genet 2007
187
20

The causality of de novo copy number variants is overestimated.
Joris R Vermeesch, Irina Balikova, Connie Schrander-Stumpel, Jean-Pierre Fryns, Koenraad Devriendt. Eur J Hum Genet 2011
34
20

Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages.
Anthony J Schaeffer, June Chung, Konstantina Heretis, Andrew Wong, David H Ledbetter, Christa Lese Martin. Am J Hum Genet 2004
146
20

Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to grow in vitro.
M Benkhalifa, S Kasakyan, P Clement, M Baldi, G Tachdjian, A Demirol, T Gurgan, F Fiorentino, M Mohammed, M B Qumsiyeh. Prenat Diagn 2005
90
20

A retrospective study by oligonucleotide array-CGH analysis in 50 fetuses with multiple malformations.
M Valduga, C Philippe, P Bach Segura, O Thiebaugeorges, A Miton, M Beri, C Bonnet, C Nemos, B Foliguet, P Jonveaux. Prenat Diagn 2010
54
20

Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype.
Linda Kleeman, Diana W Bianchi, Lisa G Shaffer, Emily Rorem, Janet Cowan, Sabrina D Craigo, Hocine Tighiouart, Louise E Wilkins-Haug. Prenat Diagn 2009
78
20

Cryptic chromosomal abnormalities identified in children with congenital heart disease.
Ashleigh A Richards, Lane Jaeckle Santos, Haley A Nichols, Bill P Crider, Frederick F Elder, Natalie S Hauser, Andrew R Zinn, Vidu Garg. Pediatr Res 2008
66
20

Challenges of interpreting copy number variation in syndromic and non-syndromic congenital heart defects.
J Breckpot, B Thienpont, Y Arens, L C Tranchevent, J R Vermeesch, Y Moreau, M Gewillig, K Devriendt. Cytogenet Genome Res 2011
42
20

High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease.
F Erdogan, L A Larsen, L Zhang, Z Tümer, N Tommerup, W Chen, J R Jacobsen, M Schubert, J Jurkatis, A Tzschach,[...]. J Med Genet 2008
91
20

Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations.
Paola Evangelidou, Carolina Sismani, Marios Ioannides, Christodoulos Christodoulou, George Koumbaris, Ioannis Kallikas, Ioannis Georgiou, Voula Velissariou, Philippos C Patsalis. Mol Cytogenet 2010
31
20


Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing.
S L van der Steen, K E M Diderich, S R Riedijk, J Verhagen-Visser, L C P Govaerts, M Joosten, M F C M Knapen, D Van Opstal, M I Srebniak, A Tibben,[...]. Clin Genet 2015
32
20

A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors.
Paul Daniel Brady, Barbara Delle Chiaie, Gabrielle Christenhusz, Kris Dierickx, Kris Van Den Bogaert, Bjorn Menten, Sandra Janssens, Paul Defoort, Ellen Roets, Elke Sleurs,[...]. Genet Med 2014
45
20


High-resolution microarray in the assessment of fetal anomalies detected by ultrasound.
Poonam Charan, Nicole Woodrow, Sue P Walker, Devika Ganesamoorthy, George McGillivray, Ricardo Palma-Dias. Aust N Z J Obstet Gynaecol 2014
12
20

Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotyping.
D L Bruno, S M White, D Ganesamoorthy, T Burgess, K Butler, S Corrie, D Francis, L Hills, K Prabhakara, C Ngo,[...]. J Med Genet 2011
50
20

Understanding variable expressivity in microdeletion syndromes.
Joris A Veltman, Han G Brunner. Nat Genet 2010
48
20

Genomic microarrays: a technology overview.
Paul D Brady, Joris R Vermeesch. Prenat Diagn 2012
28
20

Genome-wide arrays: quality criteria and platforms to be used in routine diagnostics.
Joris R Vermeesch, Paul D Brady, Damien Sanlaville, Klaas Kok, Rosalind J Hastings. Hum Mutat 2012
54
20

CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle,[...]. Nature 2014
378
20

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
524
20

The introduction of arrays in prenatal diagnosis: a special challenge.
Annalisa Vetro, Katelijne Bouman, Ros Hastings, Dominic J McMullan, Joris R Vermeesch, Konstantin Miller, Birgit Sikkema-Raddatz, David H Ledbetter, Orsetta Zuffardi, Conny M A van Ravenswaaij-Arts. Hum Mutat 2012
51
20

Towards an evidence-based process for the clinical interpretation of copy number variation.
E R Riggs, D M Church, K Hanson, V L Horner, E B Kaminsky, R M Kuhn, K E Wain, E S Williams, S Aradhya, H M Kearney,[...]. Clin Genet 2012
62
20

Chromosomal microarray analysis as a first-tier clinical diagnostic test: Estonian experience.
Olga Zilina, Rita Teek, Pille Tammur, Kati Kuuse, Maria Yakoreva, Eve Vaidla, Triin Mölter-Väär, Tiia Reimand, Ants Kurg, Katrin Ounap. Mol Genet Genomic Med 2014
15
20

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Erin B Kaminsky, Vineith Kaul, Justin Paschall, Deanna M Church, Brian Bunke, Dawn Kunig, Daniel Moreno-De-Luca, Andres Moreno-De-Luca, Jennifer G Mulle, Stephen T Warren,[...]. Genet Med 2011
288
20

Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges.
Olivier Vanakker, Catheline Vilain, Katrien Janssens, Nathalie Van der Aa, Guillaume Smits, Claude Bandelier, Bettina Blaumeiser, Saskia Bulk, Jean-Hubert Caberg, Anne De Leener,[...]. Eur J Med Genet 2014
61
20

Chromosome microarrays in human reproduction.
Evica Rajcan-Separovic. Hum Reprod Update 2012
15
20


Types of array findings detectable in cytogenetic diagnosis: a proposal for a generic classification.
Malgorzata I Srebniak, Karin E M Diderich, Lutgarde C P Govaerts, Marieke Joosten, Sam Riedijk, Robert Jan H Galjaard, Diane Van Opstal. Eur J Hum Genet 2014
27
20


Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A Filipink, Juliann S McConnell, Brad Angle, Wendy S Meschino,[...]. N Engl J Med 2012
357
20

Copy-number changes in prenatal diagnosis.
Melissa Strassberg, Gary Fruhman, Ignatia B Van den Veyver. Expert Rev Mol Diagn 2011
16
20

Association of copy number variants with specific ultrasonographically detected fetal anomalies.
Jennifer C Donnelly, Lawrence D Platt, Andrei Rebarber, Julia Zachary, William A Grobman, Ronald J Wapner. Obstet Gynecol 2014
82
20

Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases.
Ioannis Papoulidis, Alexandros Sotiriadis, Elisavet Siomou, Elena Papageorgiou, Makarios Eleftheriades, Vasilios Papadopoulos, Eirini Oikonomidou, Sandro Orru, Emmanouil Manolakos, Apostolos Athanasiadis. Prenat Diagn 2015
23
20

Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong.
Anita S Y Kan, Elizabeth T Lau, W F Tang, Sario S Y Chan, Simon C K Ding, Kelvin Y K Chan, C P Lee, Pui Wah Hui, Brian H Y Chung, K Y Leung,[...]. PLoS One 2014
30
20

Detection of submicroscopic chromosomal aberrations by array-based comparative genomic hybridization in fetuses with congenital heart disease.
Y Yan, Q Wu, L Zhang, X Wang, S Dan, D Deng, L Sun, L Yao, Y Ma, L Wang. Ultrasound Obstet Gynecol 2014
31
20

Chromosomal microarray use among women undergoing invasive prenatal diagnosis.
Mariam Naqvi, Ilona T Goldfarb, Kaitlin J Hanmer, Allison Bryant. Prenat Diagn 2016
8
25

Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high-risk indications.
Jose Carlos P Ferreira, Francesca R Grati, Komal Bajaj, Francesca Malvestiti, Maria Beatrice Grimi, Anna Trotta, Rosaria Liuti, Silvia Milani, Lara Branca, Jacob Hartman,[...]. Prenat Diagn 2016
16
20

Ultrasound screening for fetal chromosome anomalies.
A Drugan, M P Johnson, M I Evans. Am J Med Genet 2000
16
10

Prenatal detection of unbalanced chromosomal rearrangements by array CGH.
L Rickman, H Fiegler, C Shaw-Smith, R Nash, V Cirigliano, G Voglino, B L Ng, C Scott, J Whittaker, M Adinolfi,[...]. J Med Genet 2006
94
10

Microarray analysis for constitutional cytogenetic abnormalities.
Lisa G Shaffer, Arthur L Beaudet, Arthur R Brothman, Betsy Hirsch, Brynn Levy, Christa Lese Martin, James T Mascarello, Kathleen W Rao. Genet Med 2007
50
10

Uniparental disomy and human disease: an overview.
Kazuki Yamazawa, Tsutomu Ogata, Anne C Ferguson-Smith. Am J Med Genet C Semin Med Genet 2010
107
10

Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.
Andrew B Sparks, Eric T Wang, Craig A Struble, Wade Barrett, Renee Stokowski, Celeste McBride, Jacob Zahn, Kevin Lee, Naiping Shen, Jigna Doshi,[...]. Prenat Diagn 2012
176
10

Noninvasive prenatal testing/noninvasive prenatal diagnosis: the position of the National Society of Genetic Counselors.
Patricia L Devers, Amy Cronister, Kelly E Ormond, Flavia Facio, Campbell K Brasington, Pamela Flodman. J Genet Couns 2013
134
10

Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohort.
Julia Baptista, Catherine Mercer, Elena Prigmore, Susan M Gribble, Nigel P Carter, Viv Maloney, N Simon Thomas, Patricia A Jacobs, John A Crolla. Am J Hum Genet 2008
115
10

Comparison of chromosome analysis and chromosomal microarray analysis: what is the value of chromosome analysis in today's genomic array era?
Weimin Bi, Caroline Borgan, Amber N Pursley, Patricia Hixson, Chad A Shaw, Carlos A Bacino, Seema R Lalani, Ankita Patel, Pawel Stankiewicz, James R Lupski,[...]. Genet Med 2013
38
10


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.