. Obstet Gynecol 2017
Times Cited: 17
Times Cited: 17
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
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
17
Expanded carrier screening in reproductive medicine-points to consider: a joint statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal Quality Foundation, and Society for Maternal-Fetal Medicine.
Janice G Edwards, Gerald Feldman, James Goldberg, Anthony R Gregg, Mary E Norton, Nancy C Rose, Adele Schneider, Katie Stoll, Ronald Wapner, Michael S Watson. Obstet Gynecol 2015
Janice G Edwards, Gerald Feldman, James Goldberg, Anthony R Gregg, Mary E Norton, Nancy C Rose, Adele Schneider, Katie Stoll, Ronald Wapner, Michael S Watson. Obstet Gynecol 2015
11
A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.
Heather Hampel, Robin L Bennett, Adam Buchanan, Rachel Pearlman, Georgia L Wiesner. Genet Med 2015
Heather Hampel, Robin L Bennett, Adam Buchanan, Rachel Pearlman, Georgia L Wiesner. Genet Med 2015
11
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
Erica M Bednar, Holly D Oakley, Charlotte C Sun, Catherine C Burke, Mark F Munsell, Shannon N Westin, Karen H Lu. Gynecol Oncol 2017
11
Limitations and Pitfalls of Using Family Letters to Communicate Genetic Risk: a Qualitative Study with Patients and Healthcare Professionals.
Sandi Dheensa, Anneke Lucassen, Angela Fenwick. J Genet Couns 2018
Sandi Dheensa, Anneke Lucassen, Angela Fenwick. J Genet Couns 2018
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
Álvaro Mendes, Milena Paneque, Liliana Sousa, Angus Clarke, Jorge Sequeiros. Eur J Hum Genet 2016
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
Celine H M Leenen, Mariska den Heijer, Conny van der Meer, Ernst J Kuipers, Monique E van Leerdam, Anja Wagner. Fam Cancer 2016
11
Genetic diseases and information to relatives: practical and ethical issues for professionals after introduction of a legal framework in France.
Diane d'Audiffret Van Haecke, Sandrine de Montgolfier. Eur J Hum Genet 2018
Diane d'Audiffret Van Haecke, Sandrine de Montgolfier. Eur J Hum Genet 2018
14
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
Laura E Forrest, Martin B Delatycki, Loane Skene, MaryAnne Aitken. Eur J Hum Genet 2007
11
Using a genetic test result in the care of family members: how does the duty of confidentiality apply?
Michael Parker, Anneke Lucassen. Eur J Hum Genet 2018
Michael Parker, Anneke Lucassen. Eur J Hum Genet 2018
18
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
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
11
11
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
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
11
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
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
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
Eugene Pergament, Howard Cuckle, Bernhard Zimmermann, Milena Banjevic, Styrmir Sigurjonsson, Allison Ryan, Megan P Hall, Michael Dodd, Phil Lacroute, Melissa Stosic,[...]. Obstet Gynecol 2014
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
R Akolekar, J Beta, G Picciarelli, C Ogilvie, F D'Antonio. Ultrasound Obstet Gynecol 2015
11
Telegenetics: an Update on Availability and Use of Telemedicine in Clinical Genetics Service.
Irena Vrečar, Dimitar Hristovski, Borut Peterlin. J Med Syst 2017
Irena Vrečar, Dimitar Hristovski, Borut Peterlin. J Med Syst 2017
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
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
5
MTHFR: Addressing Genetic Counseling Dilemmas Using Evidence-Based Literature.
Brooke Levenseller Levin, Elizabeth Varga. J Genet Couns 2016
Brooke Levenseller Levin, Elizabeth Varga. J Genet Couns 2016
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
Brian A Levine, Jeremy Feinstein, Queenie V Neri, Dan Goldschlag, Zev Rosenwaks, Serge Belongie, Gianpiero D Palermo. Fertil Steril 2015
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
Wayne W Grody, Barry H Thompson, Anthony R Gregg, Lora H Bean, Kristin G Monaghan, Adele Schneider, Roger V Lebo. Genet Med 2013
5
5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review.
L D Botto, Q Yang. Am J Epidemiol 2000
L D Botto, Q Yang. Am J Epidemiol 2000
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
Gabriel A Lazarin, Felicia Hawthorne, Nicholas S Collins, Elizabeth A Platt, Eric A Evans, Imran S Haque. PLoS One 2014
5
Can we make assumptions about the psychosocial impact of living as a carrier, based on studies assessing the effects of carrier testing?
Celine Lewis, Heather Skirton, Ray Jones. J Genet Couns 2011
Celine Lewis, Heather Skirton, Ray Jones. J Genet Couns 2011
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
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
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
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
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
Pamela Callum, Maria Teresa Urbina, Rena E Falk, Jorge A Alvarez-Diaz, Isaac Benjamin, Charles A Sims. Fertil Steril 2010
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
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
5
Committee Opinion No. 690 Summary: Carrier Screening in the Age of Genomic Medicine.
. Obstet Gynecol 2017
. Obstet Gynecol 2017
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
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
5
Response to Stoll and Resta.
Gabriel A Lazarin, Imran S Haque, Shivani Nazareth, Eric A Evans. Genet Med 2013
Gabriel A Lazarin, Imran S Haque, Shivani Nazareth, Eric A Evans. Genet Med 2013
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
Johnathan M Lancaster, C Bethan Powell, Lee-May Chen, Debra L Richardson. Gynecol Oncol 2015
5
When is Genomic Testing Cost-Effective? Testing for Lynch Syndrome in Patients with Newly-Diagnosed Colorectal Cancer and Their Relatives.
Scott D Grosse. Healthcare (Basel) 2015
Scott D Grosse. Healthcare (Basel) 2015
5
5
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
R Demsky, J McCuaig, M Maganti, K J Murphy, B Rosen, S R Armel. Gynecol Oncol 2013
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
Christopher P Childers, Kimberly K Childers, Melinda Maggard-Gibbons, James Macinko. J Clin Oncol 2017
5
Hereditary ovarian cancer: beyond the usual suspects.
Kathryn P Pennington, Elizabeth M Swisher. Gynecol Oncol 2012
Kathryn P Pennington, Elizabeth M Swisher. Gynecol Oncol 2012
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
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
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
Sue V Petzel, Rachel Isaksson Vogel, Tracy Bensend, Anna Leininger, Peter A Argenta, Melissa A Geller. J Genet Couns 2013
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
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
5
Improving attendance to genetic counselling services for gynaecological oncology patients.
Hanoon P Pokharel, Neville F Hacker, Lesley Andrews. Gynecol Oncol Res Pract 2018
Hanoon P Pokharel, Neville F Hacker, Lesley Andrews. Gynecol Oncol Res Pract 2018
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
Karina L Brierley, Erica Blouch, Whitney Cogswell, Jeanne P Homer, Debbie Pencarinha, Christine L Stanislaw, Ellen T Matloff. Cancer J 2012
5
Genetic testing for hereditary cancer: challenges to ethical care in rural and remote communities.
Lori D'Agincourt-Canning. HEC Forum 2004
Lori D'Agincourt-Canning. HEC Forum 2004
9
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.