A citation-based method for searching scientific literature

Barbara A Bernhardt, Danielle Soucier, Karen Hanson, Melissa S Savage, Laird Jackson, Ronald J Wapner. Genet. Med. 2013
Times Cited: 104







List of co-cited articles
599 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
51

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am. J. Hum. Genet. 2010
26

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
38

"If it helps..." the use of microarray technology in prenatal testing: patient and partners reflections.
Sarah C Hillman, John Skelton, Elizabeth Quinlan-Jones, Amie Wilson, Mark D Kilby. Am. J. Med. Genet. A 2013
24
91

An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing.
Barbara A Bernhardt, Katherine Kellom, Alexandra Barbarese, W Andrew Faucett, Ronald J Wapner. J Genet Couns 2014
34
64


ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet. Med. 2013
19

Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.
S C Hillman, D J McMullan, G Hall, F S Togneri, N James, E J Maher, C H Meller, D Williams, R J Wapner, E R Maher,[...]. Ultrasound Obstet Gynecol 2013
119
19

Comparing genetic counselor's and patient's perceptions of needs in prenatal chromosomal microarray testing.
Sarah A Walser, Katherine S Kellom, Steven C Palmer, Barbara A Bernhardt. Prenat. Diagn. 2015
22
72

Couple's Narratives of Communion and Isolation Following Abnormal Prenatal Microarray Testing Results.
Allison Werner-Lin, Frances K Barg, Katherine S Kellom, Kallyn J Stumm, Lisa Pilchman, Ashley N Tomlinson, Barbara A Bernhardt. Qual Health Res 2016
23
69

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
65

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
53

Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis.
S C Hillman, S Pretlove, A Coomarasamy, D J McMullan, E V Davison, E R Maher, M D Kilby. Ultrasound Obstet Gynecol 2011
135
14

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
29


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
13

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
45
28

Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies.
Lisa G Shaffer, Mindy P Dabell, Allan J Fisher, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Jill A Rosenfeld. Prenat. Diagn. 2012
114
12

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
12

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
33

Prenatal whole-exome sequencing: parental attitudes.
Eve J Kalynchuk, Andrew Althouse, Lisa S Parker, Devereux N Saller, Aleksandar Rajkovic. Prenat. Diagn. 2015
26
46

"Something Extra on Chromosome 5": Parents' Understanding of Positive Prenatal Chromosomal Microarray Analysis (CMA) Results.
Sarah A Walser, Allison Werner-Lin, Amita Russell, Ronald J Wapner, Barbara A Bernhardt. J Genet Couns 2016
16
75

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
406
11

"What does it mean?": uncertainties in understanding results of chromosomal microarray testing.
Marian Reiff, Barbara A Bernhardt, Surabhi Mulchandani, Danielle Soucier, Diana Cornell, Reed E Pyeritz, Nancy B Spinner. Genet. Med. 2012
66
16

Ethical controversies in prenatal microarray.
Zornitza Stark, Lynn Gillam, Susan P Walker, George McGillivray. Curr. Opin. Obstet. Gynecol. 2013
16
68

Prenatal chromosomal microarray analysis: a survey of prenatal genetic counselors' experiences and attitudes.
Marina Mikhaelian, Patricia McCarthy Veach, Ian MacFarlane, Bonnie S LeRoy, Matthew Bower. Prenat. Diagn. 2013
17
64

Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow.
Malgorzata Srebniak, Marjan Boter, GrĂ©tel Oudesluijs, Marieke Joosten, Lutgarde Govaerts, Diane Van Opstal, Robert-Jan H Galjaard. Eur. J. Hum. Genet. 2011
65
16

Exome sequencing improves genetic diagnosis of structural fetal abnormalities revealed by ultrasound.
Keren J Carss, Sarah C Hillman, Vijaya Parthiban, Dominic J McMullan, Eamonn R Maher, Mark D Kilby, Matthew E Hurles. Hum. Mol. Genet. 2014
86
12

Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N. Engl. J. Med. 2013
997
11

Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.
Ronald J Wapner, Joshua E Babiarz, Brynn Levy, Melissa Stosic, Bernhard Zimmermann, Styrmir Sigurjonsson, Nicholas Wayham, Allison Ryan, Milena Banjevic, Phil Lacroute,[...]. Am. J. Obstet. Gynecol. 2015
144
11

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
57


Promises, pitfalls and practicalities of prenatal whole exome sequencing.
Sunayna Best, Karen Wou, Neeta Vora, Ignatia B Van der Veyver, Ronald Wapner, Lyn S Chitty. Prenat. Diagn. 2018
74
14



Prenatal exome sequencing for fetuses with structural abnormalities: the next step.
S C Hillman, D Willams, K J Carss, D J McMullan, M E Hurles, M D Kilby. Ultrasound Obstet Gynecol 2015
29
34


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
24

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
13

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
9


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
14

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
14

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
29

Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities.
Suzanne Drury, Hywel Williams, Natalie Trump, Christopher Boustred, Nicholas Lench, Richard H Scott, Lyn S Chitty. Prenat. Diagn. 2015
80
11

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet. Med. 2015
9

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
50
16

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
8

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
8

Controversies in prenatal diagnosis 3: should everyone undergoing invasive testing have a microarray?
John A Crolla, Ronald Wapner, Jan M M Van Lith. Prenat. Diagn. 2014
13
61


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.