A citation-based method for searching scientific literature

Kathleen F Mittendorf, Chinedu Ukaegbu, Marian J Gilmore, Nangel M Lindberg, Tia L Kauffman, Donna J Eubanks, Elizabeth Shuster, Jake Allen, Carmit McMullen, Heather Spencer Feigelson, Katherine P Anderson, Michael C Leo, Jessica Ezzell Hunter, Sonia Okuyama Sasaki, Jamilyn M Zepp, Sapna Syngal, Benjamin S Wilfond, Katrina A B Goddard. Fam Cancer 2022
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations.
Kathleen F Mittendorf, Tia L Kauffman, Laura M Amendola, Katherine P Anderson, Barbara B Biesecker, Michael O Dorschner, Devan M Duenas, Donna J Eubanks, Heather Spencer Feigelson, Marian J Gilmore,[...]. Contemp Clin Trials 2021
7
100

Validation of Version 3.0 of the Breast Cancer Genetics Referral Screening Tool (B-RST™).
Cecelia Bellcross, April Hermstad, Christine Tallo, Christine Stanislaw. Genet Med 2019
18
66

Participant Reactions to a Literacy-Focused, Web-Based Informed Consent Approach for a Genomic Implementation Study.
Stephanie A Kraft, Kathryn M Porter, Devan M Duenas, Claudia Guerra, Galen Joseph, Sandra Soo-Jin Lee, Kelly J Shipman, Jake Allen, Donna Eubanks, Tia L Kauffman,[...]. AJOB Empir Bioeth 2021
8
66

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
947
66

Development and Validation of the PREMM5 Model for Comprehensive Risk Assessment of Lynch Syndrome.
Fay Kastrinos, Hajime Uno, Chinedu Ukaegbu, Carmelita Alvero, Ashley McFarland, Matthew B Yurgelun, Matthew H Kulke, Deborah Schrag, Jeffrey A Meyerhardt, Charles S Fuchs,[...]. J Clin Oncol 2017
82
66

Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: US Preventive Services Task Force Recommendation Statement.
Douglas K Owens, Karina W Davidson, Alex H Krist, Michael J Barry, Michael Cabana, Aaron B Caughey, Chyke A Doubeni, John W Epling, Martha Kubik, C Seth Landefeld,[...]. JAMA 2019
162
66

Health Care Segregation, Physician Recommendation, and Racial Disparities in BRCA1/2 Testing Among Women With Breast Cancer.
Anne Marie McCarthy, Mirar Bristol, Susan M Domchek, Peter W Groeneveld, Younji Kim, U Nkiru Motanya, Judy A Shea, Katrina Armstrong. J Clin Oncol 2016
95
66

Evaluating women with ovarian cancer for BRCA1 and BRCA2 mutations: missed opportunities.
Larissa A Meyer, Meaghan E Anderson, Robin A Lacour, Anuj Suri, Molly S Daniels, Diana L Urbauer, Graciela M Nogueras-Gonzalez, Kathleen M Schmeler, David M Gershenson, Karen H Lu. Obstet Gynecol 2010
90
66


The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.
Laura M Amendola, Jonathan S Berg, Carol R Horowitz, Frank Angelo, Jeannette T Bensen, Barbara B Biesecker, Leslie G Biesecker, Gregory M Cooper, Kelly East, Kelly Filipski,[...]. Am J Hum Genet 2018
61
66


Financial barriers in a county genetics clinic: Problems and solutions.
Deanna J Erwin, Christina LaMaire, Alex Espana, Tanya N Eble, Shweta U Dhar. J Genet Couns 2020
7
33

Actionable, pathogenic incidental findings in 1,000 participants' exomes.
Michael O Dorschner, Laura M Amendola, Emily H Turner, Peggy D Robertson, Brian H Shirts, Carlos J Gallego, Robin L Bennett, Kelly L Jones, Mari J Tokita, James T Bennett,[...]. Am J Hum Genet 2013
278
33

Regional models of genetic services in the United States.
Celia Kaye, Joann Bodurtha, Mathew Edick, Susanna Ginsburg, Alisha Keehn, Michele Lloyd-Puryear, Debra Lochner Doyle, Megan Lyon, Robert Ostrander, Matthew Taylor. Genet Med 2020
6
33


Effects of racial and ethnic group and health literacy on responses to genomic risk information in a medically underserved population.
Kimberly A Kaphingst, Jewel D Stafford, Lucy D'Agostino McGowan, Joann Seo, Christina R Lachance, Melody S Goodman. Health Psychol 2015
26
33

Information Mismatch: Cancer Risk Counseling with Diverse Underserved Patients.
Galen Joseph, Rena J Pasick, Dean Schillinger, Judith Luce, Claudia Guerra, Janice Ka Yan Cheng. J Genet Couns 2017
66
33


Prioritizing diversity in human genomics research.
Lucia A Hindorff, Vence L Bonham, Lawrence C Brody, Margaret E C Ginoza, Carolyn M Hutter, Teri A Manolio, Eric D Green. Nat Rev Genet 2018
160
33

A review and definition of 'usual care' in genetic counseling trials to standardize use in research.
Barbara B Biesecker, Sarah E Lillie, Laura M Amendola, Katherine E Donohue, Kelly M East, Ann Katherine M Foreman, Marian J Gilmore, Veronica Greve, Billie Liangolou, Julianne M O'Daniel,[...]. J Genet Couns 2021
4
33

Integrating stakeholder feedback in translational genomics research: an ethnographic analysis of a study protocol's evolution.
Stephanie A Kraft, Carmit McMullen, Nangel M Lindberg, David Bui, Kelly Shipman, Katherine Anderson, Galen Joseph, Devan M Duenas, Kathryn M Porter, Tia L Kauffman,[...]. Genet Med 2020
8
33

A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3.
Pablo Cingolani, Adrian Platts, Le Lily Wang, Melissa Coon, Tung Nguyen, Luan Wang, Susan J Land, Xiangyi Lu, Douglas M Ruden. Fly (Austin) 2012
33

NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 1.2020.
Mary B Daly, Robert Pilarski, Matthew B Yurgelun, Michael P Berry, Saundra S Buys, Patricia Dickson, Susan M Domchek, Ahmed Elkhanany, Susan Friedman, Judy E Garber,[...]. J Natl Compr Canc Netw 2020
175
33

Barriers to the utilization of genetic testing and genetic counseling in patients with suspected hereditary breast and ovarian cancers.
Alicia Swink, Anju Nair, Pamela Hoof, Antoinette Matthews, Chelsey Burden, Kelly Johnson, Joanne L Blum. Proc (Bayl Univ Med Cent) 2019
16
33


Comparison of Colorectal and Endometrial Microsatellite Instability Tumor Analysis and Premm5 Risk Assessment for Predicting Pathogenic Germline Variants on Multigene Panel Testing.
Alessandro Mannucci, C Sloane Furniss, Chinedu Ukaegbu, Miki Horiguchi, Tara Fehlmann, Hajime Uno, Matthew B Yurgelun, Sapna Syngal. J Clin Oncol 2020
3
33

Comparison of Universal Genetic Testing vs Guideline-Directed Targeted Testing for Patients With Hereditary Cancer Syndrome.
N Jewel Samadder, Douglas Riegert-Johnson, Lisa Boardman, Deborah Rhodes, Myra Wick, Scott Okuno, Katie L Kunze, Michael Golafshar, Pedro L S Uson, Luke Mountjoy,[...]. JAMA Oncol 2021
59
33

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
33

Racial/ethnic differences in multiple-gene sequencing results for hereditary cancer risk.
Jennifer L Caswell-Jin, Tanya Gupta, Evan Hall, Iva M Petrovchich, Meredith A Mills, Kerry E Kingham, Rachel Koff, Nicolette M Chun, Peter Levonian, Alexandra P Lebensohn,[...]. Genet Med 2018
75
33

Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women.
Leila Dorling, Sara Carvalho, Jamie Allen, Anna González-Neira, Craig Luccarini, Cecilia Wahlström, Karen A Pooley, Michael T Parsons, Cristina Fortuno, Qin Wang,[...]. N Engl J Med 2021
178
33

Development and early implementation of an Accessible, Relational, Inclusive and Actionable approach to genetic counseling: The ARIA model.
Leslie Riddle, Laura M Amendola, Marian J Gilmore, Claudia Guerra, Barbara Biesecker, Tia L Kauffman, Katherine Anderson, Alan F Rope, Michael C Leo, Mikaella Caruncho,[...]. Patient Educ Couns 2021
7
33

CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing.
Eric Talevich, A Hunter Shain, Thomas Botton, Boris C Bastian. PLoS Comput Biol 2016
683
33

Cancer genetic counseling communication with low-income Chinese immigrants.
Janice Ka Yan Cheng, Claudia Guerra, Rena J Pasick, Dean Schillinger, Judith Luce, Galen Joseph. J Community Genet 2018
16
33

Racial and Ethnic Differences in BRCA1/2 and Multigene Panel Testing Among Young Breast Cancer Patients.
T Jones, M S Trivedi, X Jiang, T Silverman, M Underhill, W K Chung, R Kukafka, K D Crew. J Cancer Educ 2021
10
33

Cultural challenges to engaging patients in shared decision making.
Sarah T Hawley, Arden M Morris. Patient Educ Couns 2017
64
33

The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
Aaron McKenna, Matthew Hanna, Eric Banks, Andrey Sivachenko, Kristian Cibulskis, Andrew Kernytsky, Kiran Garimella, David Altshuler, Stacey Gabriel, Mark Daly,[...]. Genome Res 2010
33

Current conditions in medical genetics practice.
Deborah R Maiese, Alisha Keehn, Megan Lyon, David Flannery, Michael Watson. Genet Med 2019
56
33

Radial artery versus femoral artery access options in coronary angiogram procedures: randomized controlled trial of a patient-decision aid.
Jon-David Schwalm, Dawn Stacey, Dan Pericak, Madhu K Natarajan. Circ Cardiovasc Qual Outcomes 2012
25
33

The 2019 US medical genetics workforce: a focus on clinical genetics.
Brittany D Jenkins, Catherine G Fischer, Curt A Polito, Deborah R Maiese, Alisha S Keehn, Megan Lyon, Mathew J Edick, Matthew R G Taylor, Hans C Andersson, Joann N Bodurtha,[...]. Genet Med 2021
19
33

Awareness, knowledge, perceptions, and attitudes towards genetic testing for cancer risk among ethnic minority groups: a systematic review.
Katie E J Hann, Madeleine Freeman, Lindsay Fraser, Jo Waller, Saskia C Sanderson, Belinda Rahman, Lucy Side, Sue Gessler, Anne Lanceley. BMC Public Health 2017
114
33

Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
Laura M Amendola, Michael O Dorschner, Peggy D Robertson, Joseph S Salama, Ragan Hart, Brian H Shirts, Mitzi L Murray, Mari J Tokita, Carlos J Gallego, Daniel Seung Kim,[...]. Genome Res 2015
240
33

DECIDE: a Decision Support Tool to Facilitate Parents' Choices Regarding Genome-Wide Sequencing.
Patricia Birch, S Adam, N Bansback, R R Coe, J Hicklin, A Lehman, K C Li, J M Friedman. J Genet Couns 2016
26
33

Identification of Medically Actionable Secondary Findings in the 1000 Genomes.
Emily Olfson, Catherine E Cottrell, Nicholas O Davidson, Christina A Gurnett, Jonathan W Heusel, Nathan O Stitziel, Li-Shiun Chen, Sarah Hartz, Rakesh Nagarajan, Nancy L Saccone,[...]. PLoS One 2015
57
33

Decision aids for people facing health treatment or screening decisions.
Dawn Stacey, France Légaré, Krystina Lewis, Michael J Barry, Carol L Bennett, Karen B Eden, Margaret Holmes-Rovner, Hilary Llewellyn-Thomas, Anne Lyddiatt, Richard Thomson,[...]. Cochrane Database Syst Rev 2017
33

Choosing treatment and screening options congruent with values: Do decision aids help? Sub-analysis of a systematic review.
Sarah Munro, Dawn Stacey, Krystina B Lewis, Nick Bansback. Patient Educ Couns 2016
22
33

Clinical and Counseling Experiences of Early Adopters of Whole Exome Sequencing.
Shubhangi Arora, Eden Haverfield, Gabriele Richard, Susanne B Haga, Rachel Mills. J Genet Couns 2016
13
33

A decision aid for additional findings in genomic sequencing: Development and pilot testing.
Amanda S Freed, Inga Gruß, Carmit K McMullen, Michael C Leo, Tia L Kauffman, Kathryn M Porter, Kristin R Muessig, Donna Eubanks, Katrina A B Goddard, Benjamin S Wilfond,[...]. Patient Educ Couns 2021
4
33

How digital tools can advance quality and equity in genomic medicine.
Yvonne Bombard, Robin Z Hayeems. Nat Rev Genet 2020
15
33

Validation of a decision regret scale.
Jamie C Brehaut, Annette M O'Connor, Timothy J Wood, Thomas F Hack, Laura Siminoff, Elisa Gordon, Deb Feldman-Stewart. Med Decis Making 2003
666
33

Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature.
J Delanne, S Nambot, A Chassagne, O Putois, A Pelissier, C Peyron, E Gautier, J Thevenon, E Cretin, A L Bruel,[...]. Eur J Med Genet 2019
21
33


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.