A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity



Web Platform vs In-Person Genetic Counselor for Return of Carrier Results From Exome Sequencing: A Randomized Clinical Trial.
Barbara B Biesecker, Katie L Lewis, Kendall L Umstead, Jennifer J Johnston, Erin Turbitt, Kristen P Fishler, John H Patton, Ilana M Miller, Alexis R Heidlebaugh, Leslie G Biesecker. JAMA Intern Med 2018
42
17



A universal genetic testing initiative for patients with high-grade, non-mucinous epithelial ovarian cancer and the implications for cancer treatment.
Erica M Bednar, Holly D Oakley, Charlotte C Sun, Catherine C Burke, Mark F Munsell, Shannon N Westin, Karen H Lu. Gynecol Oncol 2017
26
11


How communication of genetic information within the family is addressed in genetic counselling: a systematic review of research evidence.
Álvaro Mendes, Milena Paneque, Liliana Sousa, Angus Clarke, Jorge Sequeiros. Eur J Hum Genet 2016
34
11

Genetic testing for Lynch syndrome: family communication and motivation.
Celine H M Leenen, Mariska den Heijer, Conny van der Meer, Ernst J Kuipers, Monique E van Leerdam, Anja Wagner. Fam Cancer 2016
25
11


Communicating genetic information in families--a review of guidelines and position papers.
Laura E Forrest, Martin B Delatycki, Loane Skene, MaryAnne Aitken. Eur J Hum Genet 2007
84
11


Informing family members of individuals with Lynch syndrome: a guideline for clinical geneticists.
Fred H Menko, Cora M Aalfs, Lidewij Henneman, Yrrah Stol, Miranda Wijdenes, Ellen Otten, Marleen M J Ploegmakers, Johan Legemaate, Ellen M A Smets, Guido M W R de Wert,[...]. Fam Cancer 2013
25
11



Effect of enhanced information, values clarification, and removal of financial barriers on use of prenatal genetic testing: a randomized clinical trial.
Miriam Kuppermann, Sherri Pena, Judith T Bishop, Sanae Nakagawa, Steven E Gregorich, Anita Sit, Juan Vargas, Aaron B Caughey, Susan Sykes, Lasha Pierce,[...]. JAMA 2014
67
11


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
643
11

Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohort.
Eugene Pergament, Howard Cuckle, Bernhard Zimmermann, Milena Banjevic, Styrmir Sigurjonsson, Allison Ryan, Megan P Hall, Michael Dodd, Phil Lacroute, Melissa Stosic,[...]. Obstet Gynecol 2014
162
11

Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta-analysis.
R Akolekar, J Beta, G Picciarelli, C Ogilvie, F D'Antonio. Ultrasound Obstet Gynecol 2015
320
11

Telegenetics: an Update on Availability and Use of Telemedicine in Clinical Genetics Service.
Irena Vrečar, Dimitar Hristovski, Borut Peterlin. J Med Syst 2017
26
11


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
5

MTHFR: Addressing Genetic Counseling Dilemmas Using Evidence-Based Literature.
Brooke Levenseller Levin, Elizabeth Varga. J Genet Couns 2016
21
5

Three-dimensional sperm surface reconstruction: a novel approach to assessing sperm morphology.
Brian A Levine, Jeremy Feinstein, Queenie V Neri, Dan Goldschlag, Zev Rosenwaks, Serge Belongie, Gianpiero D Palermo. Fertil Steril 2015
2
50

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
5


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
5


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
5

Joint SOGC-CCMG Opinion for Reproductive Genetic Carrier Screening: An Update for All Canadian Providers of Maternity and Reproductive Healthcare in the Era of Direct-to-Consumer Testing.
R Douglas Wilson, Isabelle De Bie, Christine M Armour, Richard N Brown, Carla Campagnolo, June C Carroll, Nan Okun, Tanya Nelson, Rhonda Zwingerman, Francois Audibert,[...]. J Obstet Gynaecol Can 2016
17
5

Spinal muscular atrophy (SMA) after conception using gametes from anonymous donors: recommendations for the future.
Pamela Callum, Maria Teresa Urbina, Rena E Falk, Jorge A Alvarez-Diaz, Isaac Benjamin, Charles A Sims. Fertil Steril 2010
4
25

ESHRE Task Force on Ethics and Law 21: genetic screening of gamete donors: ethical issues.
W Dondorp, G De Wert, G Pennings, F Shenfield, P Devroey, B Tarlatzis, P Barri, K Diedrich, U Eichenlaub-Ritter, F Tüttelmann,[...]. Hum Reprod 2014
27
5



Expanded carrier screening in an infertile population: how often is clinical decision making affected?
Jason M Franasiak, Meir Olcha, Paul A Bergh, Kathleen H Hong, Marie D Werner, Eric J Forman, Rebekah S Zimmerman, Richard T Scott. Genet Med 2016
21
5

Response to Stoll and Resta.
Gabriel A Lazarin, Imran S Haque, Shivani Nazareth, Eric A Evans. Genet Med 2013
1
100

Society of Gynecologic Oncology statement on risk assessment for inherited gynecologic cancer predispositions.
Johnathan M Lancaster, C Bethan Powell, Lee-May Chen, Debra L Richardson. Gynecol Oncol 2015
154
5





Keeping it simple: genetics referrals for all invasive serous ovarian cancers.
R Demsky, J McCuaig, M Maganti, K J Murphy, B Rosen, S R Armel. Gynecol Oncol 2013
38
5

National Estimates of Genetic Testing in Women With a History of Breast or Ovarian Cancer.
Christopher P Childers, Kimberly K Childers, Melinda Maggard-Gibbons, James Macinko. J Clin Oncol 2017
130
5

Hereditary ovarian cancer: beyond the usual suspects.
Kathryn P Pennington, Elizabeth M Swisher. Gynecol Oncol 2012
79
5

Inherited Mutations in Women With Ovarian Carcinoma.
Barbara M Norquist, Maria I Harrell, Mark F Brady, Tom Walsh, Ming K Lee, Suleyman Gulsuner, Sarah S Bernards, Silvia Casadei, Qian Yi, Robert A Burger,[...]. JAMA Oncol 2016
335
5

Genetic risk assessment for women with epithelial ovarian cancer: referral patterns and outcomes in a university gynecologic oncology clinic.
Sue V Petzel, Rachel Isaksson Vogel, Tracy Bensend, Anna Leininger, Peter A Argenta, Melissa A Geller. J Genet Couns 2013
30
5

Mainstreaming cancer genetics: A model integrating germline BRCA testing into routine ovarian cancer clinics.
Maira Kentwell, Eryn Dow, Yoland Antill, C David Wrede, Orla McNally, Emily Higgs, Anne Hamilton, Sumitra Ananda, Geoffrey J Lindeman, Clare L Scott. Gynecol Oncol 2017
54
5

Improving attendance to genetic counselling services for gynaecological oncology patients.
Hanoon P Pokharel, Neville F Hacker, Lesley Andrews. Gynecol Oncol Res Pract 2018
2
50

Adverse events in cancer genetic testing: medical, ethical, legal, and financial implications.
Karina L Brierley, Erica Blouch, Whitney Cogswell, Jeanne P Homer, Debbie Pencarinha, Christine L Stanislaw, Ellen T Matloff. Cancer J 2012
66
5



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.