A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
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
47
50

Expanded carrier screening: A review of early implementation and literature.
Gabriel A Lazarin, Imran S Haque. Semin Perinatol 2016
33
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
61
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
117
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. J Community Genet 2014
25
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
48
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
102
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
16
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
29
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
44
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
265
25

Generic consent for genetic screening.
S Elias, G J Annas. N Engl J Med 1994
91
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
16
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
15
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
412
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
100
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
46
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
27
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
282
25


On the future of genetic risk assessment.
Hans-Hilger Ropers. J Community Genet 2012
36
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
38
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
28
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
39
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
12
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
26
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
189
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
86
12

The Cystic Fibrosis mutation "arms race": when less is more.
Wayne W Grody, Garry R Cutting, Michael S Watson. Genet Med 2007
31
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
92
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
64
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
120
12

Carrier screening in individuals of Ashkenazi Jewish descent.
Susan J Gross, Beth A Pletcher, Kristin G Monaghan. Genet Med 2008
115
12

Newborn screening showing decreasing incidence of cystic fibrosis.
Jaime E Hale, Richard B Parad, Anne Marie Comeau. N Engl J Med 2008
41
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.