A citation-based method for searching scientific literature

Rebecca Hernan, Megan T Cho, Ashley L Wilson, Priyanka Ahimaz, Catherine Au, Sara M Berger, Edwin Guzman, Michelle Primiano, Jessica E Shaw, Meredith Ross, Leyla Tabanfar, Ilana Chilton, Emily Griffin, Chana Ratner, Kwame Anyane-Yeboa, Alejandro Iglesias, Laura Pisani, Jasmin Roohi, Jimmy Duong, Josue Martinez, Paul Appelbaum, Robert Klitzman, Ruth Ottman, Wendy K Chung, Julia Wynn. Patient Educ Couns 2020
Times Cited: 6

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

Times Cited
  Times     Co-cited

Patient assessment of chatbots for the scalable delivery of genetic counseling.
Tara Schmidlen, Marci Schwartz, Kristy DiLoreto, H Lester Kirchner, Amy C Sturm. J Genet Couns 2019

Genetic Testing for Inherited Cardiovascular Diseases: A Scientific Statement From the American Heart Association.
Kiran Musunuru, Ray E Hershberger, Sharlene M Day, N Jennifer Klinedinst, Andrew P Landstrom, Victoria N Parikh, Siddharth Prakash, Christopher Semsarian, Amy C Sturm. Circ Genom Precis Med 2020

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

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

Randomized Trial of Telegenetics vs. In-Person Cancer Genetic Counseling: Cost, Patient Satisfaction and Attendance.
Adam H Buchanan, Santanu K Datta, Celette Sugg Skinner, Gail P Hollowell, Henry F Beresford, Thomas Freeland, Benjamin Rogers, John Boling, P Kelly Marcom, Martha B Adams. J Genet Couns 2015

Projecting the Supply and Demand for Certified Genetic Counselors: a Workforce Study.
Jennifer M Hoskovec, R L Bennett, M E Carey, J E DaVanzo, M Dougherty, S E Hahn, B S LeRoy, S O'Neal, J G Richardson, C A Wicklund. J Genet Couns 2018

American Society of Clinical Oncology Policy Statement Update: Genetic and Genomic Testing for Cancer Susceptibility.
Mark E Robson, Angela R Bradbury, Banu Arun, Susan M Domchek, James M Ford, Heather L Hampel, Stephen M Lipkin, Sapna Syngal, Dana S Wollins, Noralane M Lindor. J Clin Oncol 2015

The FMR1 premutation and reproduction.
Michael D Wittenberger, Randi J Hagerman, Stephanie L Sherman, Allyn McConkie-Rosell, Corrine K Welt, Robert W Rebar, Emily C Corrigan, Joe Leigh Simpson, Lawrence M Nelson. Fertil Steril 2007

SAPC Hot Topic: the importance of 'health literacy' in primary care.
Gill Rowlands, Jo Protheroe. Prim Health Care Res Dev 2012

Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers.
Sarah L Nolin, Anne Glicksman, Nicole Ersalesi, Carl Dobkin, W Ted Brown, Ru Cao, Eliot Blatt, Sachin Sah, Gary J Latham, Andrew G Hadd. Genet Med 2015

Health literacy assessment in adults with neurofibromatosis: electronic and short-form measurement using FCCHL and Health LiTT.
Vanessa L Merker, Sarah McDannold, Eric Riklin, Mojtaba Talaei-Khoei, Monica R Sheridan, Justin T Jordan, Scott R Plotkin, Ana-Maria Vranceanu. J Neurooncol 2018

Associated features in females with an FMR1 premutation.
Anne C Wheeler, Donald B Bailey, Elizabeth Berry-Kravis, Jan Greenberg, Molly Losh, Marsha Mailick, Montserrat Milà, John M Olichney, Laia Rodriguez-Revenga, Stephanie Sherman,[...]. J Neurodev Disord 2014

Expanded clinical phenotype of women with the FMR1 premutation.
Sarah M Coffey, Kylee Cook, Nicole Tartaglia, Flora Tassone, Danh V Nguyen, Ruiqin Pan, Hannah E Bronsky, Jennifer Yuhas, Mariya Borodyanskaya, Jim Grigsby,[...]. Am J Med Genet A 2008

Enhancing health literacy through co-design: development of culturally appropriate materials on genetic risk and customary consanguineous marriage.
Parveen Azam Ali, Sarah Salway, Elizabeth Such, Andrew Dearden, Matt Willox. Prim Health Care Res Dev 2019

Obstetrical and gynecological complications in fragile X carriers: a multicenter study.
C E Schwartz, J Dean, P N Howard-Peebles, M Bugge, M Mikkelsen, N Tommerup, C Hull, R Hagerman, J J Holden, R E Stevenson. Am J Med Genet 1994

Epidemiology of fragile X syndrome: a systematic review and meta-analysis.
Jessica Hunter, Oliver Rivero-Arias, Angel Angelov, Edward Kim, Iain Fotheringham, Jose Leal. Am J Med Genet A 2014

High rates of comorbid depressive and anxiety disorders among women with premutation of the FMR1 gene.
Heather A Kenna, Molly Tartter, Scott S Hall, Amy A Lightbody, Quynh Nguyen, C Paula de los Angeles, Allan L Reiss, Natalie L Rasgon. Am J Med Genet B Neuropsychiatr Genet 2013

The role of literacy in health and health care.
Darren A Dewalt, Michael P Pignone. Am Fam Physician 2005

Fragile X-Associated Neuropsychiatric Disorders (FXAND).
Randi J Hagerman, Dragana Protic, Akash Rajaratnam, Maria J Salcedo-Arellano, Elber Yuksel Aydin, Andrea Schneider. Front Psychiatry 2018

Improving women's knowledge about prenatal screening in the era of non-invasive prenatal testing for Down syndrome - development and acceptability of a low literacy decision aid.
Sian Karen Smith, Antonia Cai, Michelle Wong, Mariana S Sousa, Michelle Peate, Alec Welsh, Bettina Meiser, Rajneesh Kaur, Jane Halliday, Sharon Lewis,[...]. BMC Pregnancy Childbirth 2018

Depression and anxiety symptoms among women who carry the FMR1 premutation: impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms.
Jessica Ezzell Hunter, Mary Leslie, Gloria Novak, Debra Hamilton, Lisa Shubeck, Krista Charen, Ann Abramowitz, Michael P Epstein, Adriana Lori, Elisabeth Binder,[...]. Am J Med Genet B Neuropsychiatr Genet 2012

Needs assessment in genetic testing education: A survey of parents of children with autism spectrum disorder in the united states.
Shixi Zhao, Wei-Ju Chen, Shweta U Dhar, Tanya N Eble, Oi-Man Kwok, Lei-Shih Chen. Autism Res 2019

Improving Health Education for Women Who Carry an FMR1 Premutation.
Whitney Espinel, Krista Charen, Lillie Huddleston, Jeannie Visootsak, Stephanie Sherman. J Genet Couns 2016

The FMR1 premutation and attention-deficit hyperactivity disorder (ADHD): evidence for a complex inheritance.
Jessica Ezzell Hunter, Michael P Epstein, Stuart W Tinker, Ann Abramowitz, Stephanie L Sherman. Behav Genet 2012

Reproductive and gynecologic care of women with fragile X primary ovarian insufficiency (FXPOI).
Heather S Hipp, Krista H Charen, Jessica B Spencer, Emily G Allen, Stephanie L Sherman. Menopause 2016

Literacy and health outcomes: a systematic review of the literature.
Darren A Dewalt, Nancy D Berkman, Stacey Sheridan, Kathleen N Lohr, Michael P Pignone. J Gen Intern Med 2004

Fragile X-associated tremor/ataxia syndrome.
Paul J Hagerman, Randi J Hagerman. Ann N Y Acad Sci 2015

Investigation of phenotypes associated with mood and anxiety among male and female fragile X premutation carriers.
Jessica Ezzell Hunter, Emily Graves Allen, Ann Abramowitz, Michele Rusin, Mary Leslie, Gloria Novak, Debra Hamilton, Lisa Shubeck, Krista Charen, Stephanie L Sherman. Behav Genet 2008

Penetrance of FMR1 premutation associated pathologies in fragile X syndrome families.
Laia Rodriguez-Revenga, Irene Madrigal, Javier Pagonabarraga, Mar Xunclà, Celia Badenas, Jaime Kulisevsky, Beatriz Gomez, Montserrat Milà. Eur J Hum Genet 2009

Insights into genetics, human biology and disease gleaned from family based genomic studies.
Jennifer E Posey, Anne H O'Donnell-Luria, Jessica X Chong, Tamar Harel, Shalini N Jhangiani, Zeynep H Coban Akdemir, Steven Buyske, Davut Pehlivan, Claudia M B Carvalho, Samantha Baxter,[...]. Genet Med 2019

Comparisons of dual isogenic human iPSC pairs identify functional alterations directly caused by an epilepsy associated SCN1A mutation.
Yunyao Xie, Nathan N Ng, Olga S Safrina, Carmen M Ramos, Kevin C Ess, Philip H Schwartz, Martin A Smith, Diane K O'Dowd. Neurobiol Dis 2020

Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype.
Fatima Jaffer, Andreja Avbersek, Rosaria Vavassori, Carmen Fons, Jaume Campistol, Michela Stagnaro, Elisa De Grandis, Edvige Veneselli, Hendrik Rosewich, Melania Gianotta,[...]. Brain 2015

Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study.
Roope Männikkö, Leonie Wong, David J Tester, Michael G Thor, Richa Sud, Dimitri M Kullmann, Mary G Sweeney, Costin Leu, Sanjay M Sisodiya, David R FitzPatrick,[...]. Lancet 2018

Dissecting the genetic basis of focal cortical dysplasia: a large cohort study.
Sara Baldassari, Théo Ribierre, Elise Marsan, Homa Adle-Biassette, Sarah Ferrand-Sorbets, Christine Bulteau, Nathalie Dorison, Martine Fohlen, Marc Polivka, Sarah Weckhuysen,[...]. Acta Neuropathol 2019

Second-hit mosaic mutation in mTORC1 repressor DEPDC5 causes focal cortical dysplasia-associated epilepsy.
Théo Ribierre, Charlotte Deleuze, Alexandre Bacq, Sara Baldassari, Elise Marsan, Mathilde Chipaux, Giuseppe Muraca, Delphine Roussel, Vincent Navarro, Eric Leguern,[...]. J Clin Invest 2018

Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.
Claudia B Catarino, Joan Y W Liu, Ioannis Liagkouras, Vaneesha S Gibbons, Robyn W Labrum, Rachael Ellis, Cathy Woodward, Mary B Davis, Shelagh J Smith, J Helen Cross,[...]. Brain 2011

A two-hit story: Seizures and genetic mutation interaction sets phenotype severity in SCN1A epilepsies.
Ana Rita Salgueiro-Pereira, Fabrice Duprat, Paula A Pousinha, Alexandre Loucif, Vincent Douchamps, Cristina Regondi, Marion Ayrault, Martine Eugie, Marion I Stunault, Andrew Escayg,[...]. Neurobiol Dis 2019

Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression.
Jamie E Craig, Xikun Han, Ayub Qassim, Mark Hassall, Jessica N Cooke Bailey, Tyler G Kinzy, Anthony P Khawaja, Jiyuan An, Henry Marshall, Puya Gharahkhani,[...]. Nat Genet 2020

A quinidine non responsive novel KCNT1 mutation in an Indian infant with epilepsy of infancy with migrating focal seizures.
Priyanka Madaan, Prashant Jauhari, Aparajita Gupta, Biswaroop Chakrabarty, Sheffali Gulati. Brain Dev 2018

Lack of response to quinidine in KCNT1-related neonatal epilepsy.
Adam L Numis, Umesh Nair, Anita N Datta, Tristan T Sands, Michael S Oldham, Akash Patel, Melody Li, Elena Gazina, Steven Petrou, Maria Roberta Cilio. Epilepsia 2018

Precision therapy for epilepsy due to KCNT1 mutations: A randomized trial of oral quinidine.
Saul A Mullen, Patrick W Carney, Annie Roten, Michael Ching, Paul A Lightfoot, Leonid Churilov, Umesh Nair, Melody Li, Samuel F Berkovic, Steven Petrou,[...]. Neurology 2018

Publication bias in clinical research.
P J Easterbrook, J A Berlin, R Gopalan, D R Matthews. Lancet 1991

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.