A citation-based method for searching scientific literature

Antina de Jong, Wybo J Dondorp, Anja Krumeich, Julie Boonekamp, Jan M M van Lith, Guido M W R de Wert.  2013
Times Cited: 16







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



Times Cited
  Citation     Count
Similarity


Chromosomal microarray versus karyotyping for prenatal diagnosis.
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N. Engl. J. Med. 2012
503
37

Uptake of noninvasive prenatal testing (NIPT) in women following positive aneuploidy screening.
Shilpa Chetty, Matthew J Garabedian, Mary E Norton. Prenat. Diagn. 2013
96
37

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
25
37

Women's experiences receiving abnormal prenatal chromosomal microarray testing results.
Barbara A Bernhardt, Danielle Soucier, Karen Hanson, Melissa S Savage, Laird Jackson, Ronald J Wapner. Genet. Med. 2013
104
31

Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow.
Malgorzata Srebniak, Marjan Boter, Grétel Oudesluijs, Marieke Joosten, Lutgarde Govaerts, Diane Van Opstal, Robert-Jan H Galjaard. Eur. J. Hum. Genet. 2011
65
31

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
63
31

Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent.
Wybo Dondorp, Birgit Sikkema-Raddatz, Christine de Die-Smulders, Guido de Wert. Hum. Mutat. 2012
37
31

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
28
31

0.5 Mb array as a first-line prenatal cytogenetic test in cases without ultrasound abnormalities and its implementation in clinical practice.
Malgorzata I Srebniak, Lisanne Mout, Diane Van Opstal, Robert-Jan H Galjaard. Hum. Mutat. 2013
18
31

Microarrays as a diagnostic tool in prenatal screening strategies: ethical reflection.
Antina de Jong, Wybo J Dondorp, Merryn V E Macville, Christine E M de Die-Smulders, Jan M M van Lith, Guido M W R de Wert. Hum. Genet. 2014
23
25

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.
Santhosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, Francesca Antonacci, Priscillia Siswara, Andy Itsara, Laura Vives, Tom Walsh, Shane E McCarthy, Carl Baker,[...]. Nat. Genet. 2010
375
25


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
48
25


Attitudes of pregnant women and male partners towards non-invasive prenatal testing and widening the scope of prenatal screening.
Rachèl V van Schendel, Johanna H Kleinveld, Wybo J Dondorp, Eva Pajkrt, Danielle R M Timmermans, Kim C A Holtkamp, Margreet Karsten, Anne L Vlietstra, Augusta M A Lachmeijer, Lidewij Henneman. Eur. J. Hum. Genet. 2014
54
25

Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs.
Malgorzata I Srebniak, Karin Em Diderich, Marieke Joosten, Lutgarde Cp Govaerts, Jeroen Knijnenburg, Femke At de Vries, Marjan Boter, Debora Lont, Maarten Fcm Knapen, Merel C de Wit,[...]. Eur. J. Hum. Genet. 2016
30
25

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
240
25

Estimates of penetrance for recurrent pathogenic copy-number variations.
Jill A Rosenfeld, Bradley P Coe, Evan E Eichler, Howard Cuckle, Lisa G Shaffer. Genet. Med. 2013
141
25

Benefits and burdens of using a SNP array in pregnancies at increased risk for the common aneuploidies.
Diane Van Opstal, Femke de Vries, Lutgarde Govaerts, Marjan Boter, Debora Lont, Stefanie van Veen, Marieke Joosten, Karin Diderich, Robert-Jan Galjaard, Malgorzata I Srebniak. Hum. Mutat. 2015
31
25

The Psychological Challenges of Replacing Conventional Karyotyping with Genomic SNP Array Analysis in Prenatal Testing.
Sam Riedijk, Karin E M Diderich, Sanne L van der Steen, Lutgarde C P Govaerts, Marieke Joosten, Maarten F C M Knapen, Femke A T de Vries, Diane van Opstal, Aad Tibben, Robert-Jan H Galjaard.  2014
15
26

NIPT in a clinical setting: an analysis of uptake in the first months of clinical availability.
Joanne B Taylor, Valerie Y Chock, Louanne Hudgins. J Genet Couns 2014
32
18

Ethical controversies in prenatal microarray.
Zornitza Stark, Lynn Gillam, Susan P Walker, George McGillivray. Curr. Opin. Obstet. Gynecol. 2013
16
18

Women's Attitudes towards the Option to Choose between Karyotyping and Rapid Targeted Testing during Pregnancy.
Angelique J A Kooper, Dominique F C M Smeets, Ilse Feenstra, Lia D E Wijnberger, Robbert J P Rijnders, Rik W P Quartero, Peter F Boekkooi, John M G van Vugt, Arie P T Smits.  2013
3
100


Advances in prenatal screening: the ethical dimension.
Antina de Jong, Wybo J Dondorp, Suzanna G M Frints, Christine E M de Die-Smulders, Guido M W R de Wert. Nat. Rev. Genet. 2011
68
18


Noninvasive whole-genome sequencing of a human fetus.
Jacob O Kitzman, Matthew W Snyder, Mario Ventura, Alexandra P Lewis, Ruolan Qiu, Lavone E Simmons, Hilary S Gammill, Craig E Rubens, Donna A Santillan, Jeffrey C Murray,[...]. Sci Transl Med 2012
208
18

Public viewpoints on new non-invasive prenatal genetic tests.
Hannah R Farrimond, Susan E Kelly. Public Underst Sci 2013
26
18


Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.
Amy Breman, Amber N Pursley, Patricia Hixson, Weimin Bi, Patricia Ward, Carlos A Bacino, Chad Shaw, James R Lupski, Arthur Beaudet, Ankita Patel,[...]. Prenat. Diagn. 2012
63
18

Knowledge of prenatal screening and psychological management of test decisions.
K Dahl, L Hvidman, F S Jørgensen, U S Kesmodel. Ultrasound Obstet Gynecol 2011
28
18

Does informed decision making influence psychological outcomes after receiving a positive screening outcome?
Johanna H Kleinveld, Leo P Ten Kate, Matthijs van den Berg, John M G van Vugt, Daniëlle R M Timmermans. Prenat. Diagn. 2009
13
23

Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities.
Malgorzata I Srebniak, Marjan Boter, Gretel O Oudesluijs, Titia Cohen-Overbeek, Lutgarde Cp Govaerts, Karin Em Diderich, Renske Oegema, Maarten Fcm Knapen, Ingrid Mbh van de Laar, Marieke Joosten,[...].  2012
43
18


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
298
18

Understanding variable expressivity in microdeletion syndromes.
Joris A Veltman, Han G Brunner. Nat. Genet. 2010
44
18

A copy number variation morbidity map of developmental delay.
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat. Genet. 2011
724
18

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
36
18

The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents' Experiences.
S L van der Steen, S R Riedijk, J Verhagen-Visser, L C P Govaerts, M I Srebniak, D Van Opstal, M Joosten, M F C M Knapen, A Tibben, K E M Diderich,[...]. J Genet Couns 2016
19
18

A tiered-layered-staged model for informed consent in personal genome testing.
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur. J. Hum. Genet. 2013
46
18

Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part I-clinical impact.
Dick Oepkes, G C Lieve Page-Christiaens, Caroline J Bax, Mireille N Bekker, Catia M Bilardo, Elles M J Boon, G Heleen Schuring-Blom, Audrey B C Coumans, Brigitte H Faas, Robert-Jan H Galjaard,[...]. Prenat. Diagn. 2016
62
18

Presence of fetal DNA in maternal plasma and serum.
Y M Lo, N Corbetta, P F Chamberlain, V Rai, I L Sargent, C W Redman, J S Wainscoat. Lancet 1997
12

The choice of detecting Down syndrome: does money matter?
Clémentine Garrouste, Jérôme Le, Eric Maurin. Health Econ 2011
9
22

Genomic testing reaches into the womb.
Malorye Allison. Nat. Biotechnol. 2013
9
22

Non-invasive prenatal genetic testing: a study of public attitudes.
S E Kelly, H R Farrimond. Public Health Genomics 2012
46
12

Non-invasive prenatal testing with cell-free DNA: US physician attitudes toward implementation in clinical practice.
Thomas J Musci, Genevieve Fairbrother, Annette Batey, Jennifer Bruursema, Craig Struble, Ken Song. Prenat. Diagn. 2013
36
12


Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases.
Francesco Fiorentino, Fiorina Caiazzo, Stefania Napolitano, Letizia Spizzichino, Sara Bono, Mariateresa Sessa, Andrea Nuccitelli, Anil Biricik, Anthony Gordon, Giuseppe Rizzo,[...]. Prenat. Diagn. 2011
64
12

Reflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnostics.
Tessel Rigter, Lidewij Henneman, Ulf Kristoffersson, Alison Hall, Helger G Yntema, Pascal Borry, Holger Tönnies, Quinten Waisfisz, Mariet W Elting, Wybo J Dondorp,[...]. Hum. Mutat. 2013
37
12

Individualized choice in prenatal diagnosis: the impact of karyotyping and standalone rapid aneuploidy detection on quality of life.
E M A Boormans, E Birnie, D Oepkes, P F Boekkooi, G J Bonsel, J M M van Lith. Prenat. Diagn. 2010
11
18


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.