A citation-based method for searching scientific literature


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



Times Cited
  Citation     Count
Similarity




Obstetricians and gynecologists' practice and opinions of expanded carrier testing and noninvasive prenatal testing.
Peter Benn, Audrey R Chapman, Kristine Erickson, Mark S Defrancesco, Louise Wilkins-Haug, James F X Egan, Jay Schulkin. Prenat. Diagn. 2014
45
50

Expanded carrier screening: A review of early implementation and literature.
Gabriel A Lazarin, Imran S Haque. Semin. Perinatol. 2016
26
50

A universal carrier test for the long tail of Mendelian disease.
Balaji S Srinivasan, Eric A Evans, Jason Flannick, A Scott Patterson, Christopher C Chang, Tuan Pham, Sharon Young, Amit Kaushal, James Lee, Jessica L Jacobson,[...]. Reprod. Biomed. Online 2010
57
37

ACMG position statement on prenatal/preconception expanded carrier screening.
Wayne W Grody, Barry H Thompson, Anthony R Gregg, Lora H Bean, Kristin G Monaghan, Adele Schneider, Roger V Lebo. Genet. Med. 2013
101
37

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
37

Expanded carrier screening panels-does bigger mean better?
Sara Wienke, Kimberly Brown, Meagan Farmer, Charlie Strange.  2014
21
37

The changing landscape of carrier screening: expanding technology and options?.
Michelle L McGowan, Deborah Cho, Richard R Sharp. Health Matrix Clevel 2013
14
37

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
37

Responsible implementation of expanded carrier screening.
Lidewij Henneman, Pascal Borry, Davit Chokoshvili, Martina C Cornel, Carla G van El, Francesca Forzano, Alison Hall, Heidi C Howard, Sandra Janssens, Hülya Kayserili,[...]. Eur. J. Hum. Genet. 2016
78
37

Validation for clinical use of, and initial clinical experience with, a novel approach to population-based carrier screening using high-throughput, next-generation DNA sequencing.
Stephanie Hallam, Heather Nelson, Valerie Greger, Cynthia Perreault-Micale, Jocelyn Davie, Nicole Faulkner, Dana Neitzel, Kristie Casey, Mark A Umbarger, Niru Chennagiri,[...]. J Mol Diagn 2014
23
25

Targeted mutation screening panels expose systematic population bias in detection of cystic fibrosis risk.
Regine M Lim, Ari J Silver, Maxwell J Silver, Carlos Borroto, Brett Spurrier, Tanya C Petrossian, Jessica L Larson, Lee M Silver. Genet. Med. 2016
15
25

Knowledge and attitudes regarding expanded genetic carrier screening among women's healthcare providers.
Kaylene Ready, Imran S Haque, Balaji S Srinivasan, John R Marshall. Fertil. Steril. 2012
24
25

Systematic Classification of Disease Severity for Evaluation of Expanded Carrier Screening Panels.
Gabriel A Lazarin, Felicia Hawthorne, Nicholas S Collins, Elizabeth A Platt, Eric A Evans, Imran S Haque. PLoS ONE 2014
35
25

Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel.
Michael S Watson, Garry R Cutting, Robert J Desnick, Deborah A Driscoll, Katherine Klinger, Michael Mennuti, Glenn E Palomaki, Bradley W Popovich, Victoria M Pratt, Elizabeth M Rohlfs,[...]. Genet. Med. 2004
253
25

Generic consent for genetic screening.
S Elias, G J Annas. N. Engl. J. Med. 1994
86
25

Do people from the Jewish community prefer ancestry-based or pan-ethnic expanded carrier screening?
Kim C A Holtkamp, Merel C van Maarle, Maria J E Schouten, Wybo J Dondorp, Phillis Lakeman, Lidewij Henneman. Eur. J. Hum. Genet. 2016
14
25

Genetic Counselors' Perspectives and Practices Regarding Expanded Carrier Screening after Initial Clinical Availability.
Gabriel A Lazarin, Stacey Detweiler, Shivani B Nazareth, Elena Ashkinadze. J Genet Couns 2016
12
25

Carrier screening for spinal muscular atrophy.
Thomas W Prior. Genet. Med. 2008
103
25


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
388
25

Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research.
Anna Middleton, Katherine I Morley, Eugene Bragin, Helen V Firth, Matthew E Hurles, Caroline F Wright, Michael Parker. Eur. J. Hum. Genet. 2016
82
25

Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibility.
Angela R Bradbury, Linda Patrick-Miller, Jessica Long, Jacquelyn Powers, Jill Stopfer, Andrea Forman, Christina Rybak, Kristin Mattie, Amanda Brandt, Rachelle Chambers,[...]. Genet. Med. 2015
38
25

Calling for a bold new vision of health disparities intervention research.
Lisa A Cooper, Alexander N Ortega, Alice S Ammerman, Dedra Buchwald, Electra D Paskett, Lynda H Powell, Beti Thompson, Katherine L Tucker, Richard B Warnecke, William J McCarthy,[...]. Am J Public Health 2015
26
25

Digital multimedia: a new approach for informed consent?
Alan R Tait, Terri Voepel-Lewis. JAMA 2015
22
25



Laboratory standards and guidelines for population-based cystic fibrosis carrier screening.
W W Grody, G R Cutting, K W Klinger, C S Richards, M S Watson, R J Desnick. Genet. Med. 2001
272
25



Changing trends in carrier screening for genetic disease in the United States.
Shivani B Nazareth, Gabriel A Lazarin, James D Goldberg. Prenat. Diagn. 2015
28
25


"Is It Worth Knowing?" Focus Group Participants' Perceived Utility of Genomic Preconception Carrier Screening.
Jennifer L Schneider, Katrina A B Goddard, James Davis, Benjamin Wilfond, Tia L Kauffman, Jacob A Reiss, Marian Gilmore, Patricia Himes, Frances L Lynch, Michael C Leo,[...]. J Genet Couns 2016
27
25

Attitudes of European Geneticists Regarding Expanded Carrier Screening.
Sandra Janssens, Davit Chokoshvili, Danya Vears, Anne De Paepe, Pascal Borry. J Obstet Gynecol Neonatal Nurs 2017
12
25


Population-based preconception carrier screening: how potential users from the general population view a test for 50 serious diseases.
Mirjam Plantinga, Erwin Birnie, Kristin M Abbott, Richard J Sinke, Anneke M Lucassen, Juliette Schuurmans, Seyma Kaplan, Marian A Verkerk, Adelita V Ranchor, Irene M van Langen. Eur. J. Hum. Genet. 2016
31
25

Stakeholder perspectives on the implementation of genetic carrier screening in a changing landscape.
Kim C A Holtkamp, Evelien M Vos, Tessel Rigter, Phillis Lakeman, Lidewij Henneman, Martina C Cornel. BMC Health Serv Res 2017
9
25

Experiences among Women with Positive Prenatal Expanded Carrier Screening Results.
Erin Rothwell, Erin Johnson, Amber Mathiesen, Kylie Golden, Audrey Metcalf, Nancy C Rose, Jeffrey R Botkin. J Genet Couns 2017
19
25

Public expectations for return of results from large-cohort genetic research.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Bioeth 2008
183
25


Experience with carrier screening and prenatal diagnosis for 16 Ashkenazi Jewish genetic diseases.
Stuart A Scott, Lisa Edelmann, Liu Liu, Minjie Luo, Robert J Desnick, Ruth Kornreich. Hum. Mutat. 2010
83
12

The Cystic Fibrosis mutation "arms race": when less is more.
Wayne W Grody, Garry R Cutting, Michael S Watson. Genet. Med. 2007
30
12

No change in the age of diagnosis for fragile x syndrome: findings from a national parent survey.
Donald B Bailey, Melissa Raspa, Ellen Bishop, David Holiday. Pediatrics 2009
86
12

Natural history of infantile G(M2) gangliosidosis.
Annette E Bley, Ourania A Giannikopoulos, Doug Hayden, Kim Kubilus, Cynthia J Tifft, Florian S Eichler. Pediatrics 2011
51
12


An empirical estimate of carrier frequencies for 400+ causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individuals.
Gabriel A Lazarin, Imran S Haque, Shivani Nazareth, Kevin Iori, A Scott Patterson, Jessica L Jacobson, John R Marshall, William K Seltzer, Pasquale Patrizio, Eric A Evans,[...]. Genet. Med. 2013
109
12

Carrier screening in individuals of Ashkenazi Jewish descent.
Susan J Gross, Beth A Pletcher, Kristin G Monaghan. Genet. Med. 2008
111
12

Newborn screening showing decreasing incidence of cystic fibrosis.
Jaime E Hale, Richard B Parad, Anne Marie Comeau. N. Engl. J. Med. 2008
39
12

Detection of carriers in the Ashkenazi Jewish population: an objective comparison of high-throughput genotyping versus gene-by-gene testing.
Susan Klugman, Nicole Schreiber-Agus, Shivani Nazareth, Eric A Evans. Genet Test Mol Biomarkers 2013
2
50


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.