A citation-based method for searching scientific literature

Michelle L McGowan, Deborah Cho, Richard R Sharp. Health Matrix Clevel 2013
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity



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
170
64


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
430
57

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
53
50

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
120
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
64
42

Changing trends in carrier screening for genetic disease in the United States.
Shivani B Nazareth, Gabriel A Lazarin, James D Goldberg. Prenat Diagn 2015
44
42

Expanded carrier screening panels-does bigger mean better?
Sara Wienke, Kimberly Brown, Meagan Farmer, Charlie Strange. J Community Genet 2014
30
42


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
131
35


Expanded carrier screening: A review of early implementation and literature.
Gabriel A Lazarin, Imran S Haque. Semin Perinatol 2016
36
35


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
31
35

On the future of genetic risk assessment.
Hans-Hilger Ropers. J Community Genet 2012
41
35

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
288
28


Preconceptional genetic carrier testing and the commercial offer directly-to-consumers.
Pascal Borry, Lidewij Henneman, Phillis Lakeman, Leo P ten Kate, Martina C Cornel, Heidi C Howard. Hum Reprod 2011
58
28

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
50
28

Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research.
Liane Ioannou, Belinda J McClaren, John Massie, Sharon Lewis, Sylvia A Metcalfe, Laura Forrest, Martin B Delatycki. Genet Med 2014
41
28

"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
31
28

Preconception care and genetic risk: ethical issues.
Guido M W R De Wert, Wybo J Dondorp, Bartha M Knoppers. J Community Genet 2012
44
28

Development and performance of a comprehensive targeted sequencing assay for pan-ethnic screening of carrier status.
Alice K Tanner, C Alexander Valencia, Devin Rhodenizer, Marina Espirages, Cristina Da Silva, Lisa Borsuk, Sara Caldwell, Edward Gregg, Elizabeth Grimes, Agnieszka M Lichanska,[...]. J Mol Diagn 2014
15
28


EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.
Joanne Traeger-Synodinos, Cornelis L Harteveld, John M Old, Mary Petrou, Renzo Galanello, Piero Giordano, Michael Angastioniotis, Barbara De la Salle, Shirley Henderson, Alison May. Eur J Hum Genet 2015
39
21

Cystic fibrosis carrier testing in pregnancy in Canada.
R Douglas Wilson, Gregory Davies, Valerie Desilets, Gregory J Reid, Dorothy Shaw, Anne Summers, Philip Wyatt, David Young, Joan Crane, Anthony Armson,[...]. J Obstet Gynaecol Can 2002
13
23

Considering the cost of expanded carrier screening panels.
Katie Stoll, Robert Resta. Genet Med 2013
13
23

The case for universal prenatal genetic counseling.
Howard Minkoff, Richard Berkowitz. Obstet Gynecol 2014
16
21


Possibilities and barriers in the implementation of a preconceptional screening programme for cystic fibrosis carriers: a focus group study.
F A M Poppelaars, G van der Wal, J C C Braspenning, M C Cornel, L Henneman, M W Langendam, L P ten Kate. Public Health 2003
27
21



Carrier testing for Ashkenazi Jewish disorders in the prenatal setting: navigating the genetic maze.
Jose Carlos P Ferreira, Nicole Schreiber-Agus, Suzanne M Carter, Susan Klugman, Anthony R Gregg, Susan J Gross. Am J Obstet Gynecol 2014
17
21

Content analysis: method, applications, and issues.
B Downe-Wamboldt. Health Care Women Int 1992
643
21

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
14


Preconceptional ancestry-based carrier couple screening for cystic fibrosis and haemoglobinopathies: what determines the intention to participate or not and actual participation?
Phillis Lakeman, Anne Marie Catharina Plass, Lidewij Henneman, Pieter Dirk Bezemer, Martina Cornelia Cornel, Leo Pieter ten Kate. Eur J Hum Genet 2009
34
14

Attitudes of cystic fibrosis patients and parents toward carrier screening and related reproductive issues.
Sandra Janssens, Davit Chokoshvilli, Carmen Binst, Inge Mahieu, Lidewij Henneman, Anne De Paepe, Pascal Borry. Eur J Hum Genet 2016
17
14

Offering preconceptional cystic fibrosis carrier couple screening in the absence of established preconceptional care services.
Lidewij Henneman, Inge Bramsen, Linda van Kempen, Manita B van Acker, Gerard Pals, Henriette E van der Horst, Herman J Adèr, Henk M van der Ploeg, Leo P ten Kate. Community Genet 2003
35
14

Patients' ratings of genetic conditions validate a taxonomy to simplify decisions about preconception carrier screening via genome sequencing.
Michael C Leo, Carmit McMullen, Benjamin S Wilfond, Frances L Lynch, Jacob A Reiss, Marian J Gilmore, Patricia Himes, Tia L Kauffman, James V Davis, Gail P Jarvik,[...]. Am J Med Genet A 2016
16
14

Population-based genetic screening for cystic fibrosis: attitudes and outcomes.
L Ioannou, J Massie, V Collins, B McClaren, M B Delatycki. Public Health Genomics 2010
20
14

Information preferences of high literacy pregnant women regarding informed consent models for genetic carrier screening.
K E Ormond, S Banuvar, A Daly, M Iris, J Minogue, S Elias. Patient Educ Couns 2009
17
14

Distribution of CFTR mutations in Saguenay- Lac-Saint-Jean: proposal of a panel of mutations for population screening.
Anne-Marie Madore, Claude Prévost, Ruslan Dorfman, Chelsea Taylor, Peter Durie, Julian Zielenski, Catherine Laprise. Genet Med 2008
9
22

Fetal and perinatal autopsy in prenatally diagnosed fetal abnormalities with normal karyotype.
Valérie Désilets, Luc Laurier Oligny. J Obstet Gynaecol Can 2011
15
14


Genetic epidemiology of cystic fibrosis in Saguenay-Lac-St-Jean (Quebec, Canada).
J Daigneault, G Aubin, F Simard, M De Braekeleer. Clin Genet 1991
26
14


Non-invasive prenatal diagnosis for cystic fibrosis: detection of paternal mutations, exploration of patient preferences and cost analysis.
Melissa Hill, Philip Twiss, Talitha I Verhoef, Suzanne Drury, Fiona McKay, Sarah Mason, Lucy Jenkins, Stephen Morris, Lyn S Chitty. Prenat Diagn 2015
44
14

Cystic fibrosis mutations in French Canadians: three CFTR mutations are relatively frequent in a Quebec population with an elevated incidence of cystic fibrosis.
R Rozen, M De Braekeleer, J Daigneault, L Ferreira-Rajabi, M Gerdes, L Lamoureux, G Aubin, F Simard, T M Fujiwara, K Morgan. Am J Med Genet 1992
75
14


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.