A citation-based method for searching scientific literature

Wybo Dondorp, Birgit Sikkema-Raddatz, Christine de Die-Smulders, Guido de Wert. Hum Mutat 2012
Times Cited: 42

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

Times Cited
  Times     Co-cited

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

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

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

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

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

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

Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur J Hum Genet 2013

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

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

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

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

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

Point-counterpoint. Patient autonomy and incidental findings in clinical genomics.
Susan M Wolf, George J Annas, Sherman Elias. Science 2013

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

Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study.
Rossa W K Chiu, Ranjit Akolekar, Yama W L Zheng, Tak Y Leung, Hao Sun, K C Allen Chan, Fiona M F Lun, Attie T J I Go, Elizabeth T Lau, William W K To,[...]. BMJ 2011

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

Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families.
M Reiff, K Ross, S Mulchandani, K J Propert, R E Pyeritz, N B Spinner, B A Bernhardt. Clin Genet 2013

Carrier testing for severe childhood recessive diseases by next-generation sequencing.
Callum J Bell, Darrell L Dinwiddie, Neil A Miller, Shannon L Hateley, Elena E Ganusova, Joann Mudge, Ray J Langley, Lu Zhang, Clarence C Lee, Faye D Schilkey,[...]. Sci Transl Med 2011

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

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

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

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

Diagnostic interpretation of array data using public databases and internet sources.
Nicole de Leeuw, Trijnie Dijkhuizen, Jayne Y Hehir-Kwa, Nigel P Carter, Lars Feuk, Helen V Firth, Robert M Kuhn, David H Ledbetter, Christa Lese Martin, Conny M A van Ravenswaaij-Arts,[...]. Hum Mutat 2012

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

Exploring concordance and discordance for return of incidental findings from clinical sequencing.
Robert C Green, Jonathan S Berg, Gerard T Berry, Leslie G Biesecker, David P Dimmock, James P Evans, Wayne W Grody, Madhuri R Hegde, Sarah Kalia, Bruce R Korf,[...]. Genet Med 2012

To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts.
Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Hum Genet 2013

New challenges for informed consent through whole genome array testing.
C Netzer, C Klein, J Kohlhase, C Kubisch. J Med Genet 2009

Genetic testing in asymptomatic minors: background considerations towards ESHG Recommendations.
Pascal Borry, Gerry Evers-Kiebooms, Martina C Cornel, Angus Clarke, Kris Dierickx. Eur J Hum Genet 2009

Feedback of individual genetic results to research participants: in favor of a qualified disclosure policy.
Annelien L Bredenoord, N Charlotte Onland-Moret, Johannes J M Van Delden. Hum Mutat 2011

Next-generation sequencing: does the next generation still have a right to an open future?
Annelien L Bredenoord, Martine C de Vries, Johannes J M van Delden. Nat Rev Genet 2013

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

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

"I want to know what's in Pandora's Box": comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing.
Anne Townsend, Shelin Adam, Patricia H Birch, Zoe Lohn, Francois Rousseau, Jan M Friedman. Am J Med Genet A 2012

Stakeholders' opinions on the implementation of pediatric whole exome sequencing: implications for informed consent.
Brooke L Levenseller, Danielle J Soucier, Victoria A Miller, Diana Harris, Laura Conway, Barbara A Bernhardt. J Genet Couns 2014

The scope of prenatal diagnosis for women at increased risk for aneuploidies: views and preferences of professionals and potential users.
Antina de Jong, Wybo J Dondorp, Anja Krumeich, Julie Boonekamp, Jan M M van Lith, Guido M W R de Wert. J Community Genet 2013

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

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases.
Ignatia B Van den Veyver, Ankita Patel, Chad A Shaw, Amber N Pursley, Sung-Hae L Kang, Marcia J Simovich, Patricia A Ward, Sandra Darilek, Anthony Johnson, Sarah E Neill,[...]. Prenat Diagn 2009

Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post-array CGH era?
The-Hung Bui, Annalisa Vetro, Orsetta Zuffardi, Lisa G Shaffer. Prenat Diagn 2011

Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives.
Sandra Darilek, Patricia Ward, Amber Pursley, Katie Plunkett, Patti Furman, Pilar Magoulas, Ankita Patel, Sau Wai Cheung, Christine M Eng. Genet Med 2008

Whole-genome sequencing and the physician.
A Thorogood, B M Knoppers, W J Dondorp, G M W R de Wert. Clin Genet 2012

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.