A citation-based method for searching scientific literature

David T Miller, Kristy Lee, Adam S Gordon, Laura M Amendola, Kathy Adelman, Sherri J Bale, Wendy K Chung, Michael H Gollob, Steven M Harrison, Gail E Herman, Ray E Hershberger, Teri E Klein, Kent McKelvey, C Sue Richards, Christopher N Vlangos, Douglas R Stewart, Michael S Watson, Christa Lese Martin. Genet Med 2021
Times Cited: 16

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

Times Cited
  Times     Co-cited

ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG).
David T Miller, Kristy Lee, Wendy K Chung, Adam S Gordon, Gail E Herman, Teri E Klein, Douglas R Stewart, Laura M Amendola, Kathy Adelman, Sherri J Bale,[...]. Genet Med 2021

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

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013

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

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
M Ragan Hart, Barbara B Biesecker, Carrie L Blout, Kurt D Christensen, Laura M Amendola, Katie L Bergstrom, Sawona Biswas, Kevin M Bowling, Kyle B Brothers, Laura K Conlin,[...]. Genet Med 2019

Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.
Michael P Mackley, Benjamin Fletcher, Michael Parker, Hugh Watkins, Elizabeth Ormondroyd. Genet Med 2017

CardioClassifier: disease- and gene-specific computational decision support for clinical genome interpretation.
Nicola Whiffin, Roddy Walsh, Risha Govind, Matthew Edwards, Mian Ahmad, Xiaolei Zhang, Upasana Tayal, Rachel Buchan, William Midwinter, Alicja E Wilk,[...]. Genet Med 2018

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020

Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.
Rafik Tadros, Catherine Francis, Xiao Xu, Alexa M C Vermeer, Andrew R Harper, Roy Huurman, Ken Kelu Bisabu, Roddy Walsh, Edgar T Hoorntje, Wouter P Te Rijdt,[...]. Nat Genet 2021

Reclassification of genetic variants in children with long QT syndrome.
Dominik S Westphal, Tobias Burkard, Alexander Moscu-Gregor, Roman Gebauer, Gabriele Hessling, Cordula M Wolf. Mol Genet Genomic Med 2020

Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants.
Christopher M Haggerty, Scott M Damrauer, Michael G Levin, David Birtwell, David J Carey, Alicia M Golden, Dustin N Hartzel, Yirui Hu, Renae Judy, Melissa A Kelly,[...]. Circulation 2019

Evidence-Based Assessment of Genes in Dilated Cardiomyopathy.
Elizabeth Jordan, Laiken Peterson, Tomohiko Ai, Babken Asatryan, Lucas Bronicki, Emily Brown, Rudy Celeghin, Matthew Edwards, Judy Fan, Jodie Ingles,[...]. Circulation 2021

Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
Roddy Walsh, Kate L Thomson, James S Ware, Birgit H Funke, Jessica Woodley, Karen J McGuire, Francesco Mazzarotto, Edward Blair, Anneke Seller, Jenny C Taylor,[...]. Genet Med 2017

Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert Panel.
Melissa A Kelly, Colleen Caleshu, Ana Morales, Jillian Buchan, Zena Wolf, Steven M Harrison, Stuart Cook, Mitchell W Dillon, John Garcia, Eden Haverfield,[...]. Genet Med 2018

Titin-truncating variants affect heart function in disease cohorts and the general population.
Sebastian Schafer, Antonio de Marvao, Eleonora Adami, Lorna R Fiedler, Benjamin Ng, Ester Khin, Owen J L Rackham, Sebastiaan van Heesch, Chee J Pua, Miao Kui,[...]. Nat Genet 2017

UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age.
Cathie Sudlow, John Gallacher, Naomi Allen, Valerie Beral, Paul Burton, John Danesh, Paul Downey, Paul Elliott, Jane Green, Martin Landray,[...]. PLoS Med 2015

Impact of variant reclassification in the clinical setting of cardiovascular genetics.
Rebecca E VanDyke, Sayaka Hashimoto, Ana Morales, Robert E Pyatt, Amy C Sturm. J Genet Couns 2021

Incidental and clinically actionable genetic variants in 1005 whole exomes and genomes from Qatar.
Abhinav Jain, Shrey Gandhi, Remya Koshy, Vinod Scaria. Mol Genet Genomics 2018

2020 AHA/ACC Guideline for the Diagnosis and Treatment of Patients With Hypertrophic Cardiomyopathy: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines.
Steve R Ommen, Seema Mital, Michael A Burke, Sharlene M Day, Anita Deswal, Perry Elliott, Lauren L Evanovich, Judy Hung, José A Joglar, Paul Kantor,[...]. J Am Coll Cardiol 2020

Penetrance of Hypertrophic Cardiomyopathy in Sarcomere Protein Mutation Carriers.
Massimiliano Lorenzini, Gabrielle Norrish, Ella Field, Juan Pablo Ochoa, Marcos Cicerchia, Mohammed M Akhtar, Petros Syrris, Luis R Lopes, Juan Pablo Kaski, Perry M Elliott. J Am Coll Cardiol 2020

Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity.
Andrew R Harper, Anuj Goel, Christopher Grace, Kate L Thomson, Steffen E Petersen, Xiao Xu, Adam Waring, Elizabeth Ormondroyd, Christopher M Kramer, Carolyn Y Ho,[...]. Nat Genet 2021

Revisiting the Diagnostic Yield of Hypertrophic Cardiomyopathy Genetic Testing.
Alexandra Butters, Richard D Bagnall, Jodie Ingles. Circ Genom Precis Med 2020

2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC).
Perry M Elliott, Aris Anastasakis, Michael A Borger, Martin Borggrefe, Franco Cecchi, Philippe Charron, Albert Alain Hagege, Antoine Lafont, Giuseppe Limongelli, Heiko Mahrholdt,[...]. Eur Heart J 2014

New perspectives on the prevalence of hypertrophic cardiomyopathy.
Christopher Semsarian, Jodie Ingles, Martin S Maron, Barry J Maron. J Am Coll Cardiol 2015

Outcomes of Contemporary Family Screening in Hypertrophic Cardiomyopathy.
Hannah G van Velzen, Arend F L Schinkel, Sara J Baart, Rogier A Oldenburg, Ingrid M E Frohn-Mulder, Marjon A van Slegtenhorst, Michelle Michels. Circ Genom Precis Med 2018

Phenotypic Expression and Outcomes in Individuals With Rare Genetic Variants of Hypertrophic Cardiomyopathy.
Antonio de Marvao, Kathryn A McGurk, Sean L Zheng, Marjola Thanaj, Wenjia Bai, Jinming Duan, Carlo Biffi, Francesco Mazzarotto, Ben Statton, Timothy J W Dawes,[...]. J Am Coll Cardiol 2021

Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial.
Yvonne Bombard, Marc Clausen, Salma Shickh, Chloe Mighton, Selina Casalino, Theresa H M Kim, Sarah M Muir, Lindsay Carlsson, Nancy Baxter, Adena Scheer,[...]. Genet Med 2020

Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline.
Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, Daniel P Judge, Paul F Kantor, Kim L McBride, Ana Morales, Matthew R G Taylor, Matteo Vatta, Stephanie M Ware. J Card Fail 2018

Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data.
Michael H Guo, Lacey Plummer, Yee-Ming Chan, Joel N Hirschhorn, Margaret F Lippincott. Am J Hum Genet 2018

Rare variant analysis for family-based design.
Gourab De, Wai-Ki Yip, Iuliana Ionita-Laza, Nan Laird. PLoS One 2013

Heritability of left ventricular dimensions and mass in American Indians: The Strong Heart Study.
Jonathan N Bella, Jean W MacCluer, Mary J Roman, Laura Almasy, Kari E North, Lyle G Best, Elisa T Lee, Richard R Fabsitz, Barbara V Howard, Richard B Devereux. J Hypertens 2004

Toward Genetics-Driven Early Intervention in Dilated Cardiomyopathy: Design and Implementation of the DCM Precision Medicine Study.
Daniel D Kinnamon, Ana Morales, Deborah J Bowen, Wylie Burke, Ray E Hershberger. Circ Cardiovasc Genet 2017

Rare-variant association testing for sequencing data with the sequence kernel association test.
Michael C Wu, Seunggeun Lee, Tianxi Cai, Yun Li, Michael Boehnke, Xihong Lin. Am J Hum Genet 2011

A reference panel of 64,976 haplotypes for genotype imputation.
Shane McCarthy, Sayantan Das, Warren Kretzschmar, Olivier Delaneau, Andrew R Wood, Alexander Teumer, Hyun Min Kang, Christian Fuchsberger, Petr Danecek, Kevin Sharp,[...]. Nat Genet 2016

Racial differences in incident heart failure among young adults.
Kirsten Bibbins-Domingo, Mark J Pletcher, Feng Lin, Eric Vittinghoff, Julius M Gardin, Alexander Arynchyn, Cora E Lewis, O Dale Williams, Stephen B Hulley. N Engl J Med 2009

Clinical characteristics of 304 kindreds evaluated for familial dilated cardiomyopathy.
Jessica D Kushner, Deirdre Nauman, Donna Burgess, Susan Ludwigsen, Sharie B Parks, George Pantely, Emily Burkett, Ray E Hershberger. J Card Fail 2006

Genotype-phenotype correlations in recessive titinopathies.
Marco Savarese, Anna Vihola, Emily C Oates, Rita Barresi, Chiara Fiorillo, Giorgio Tasca, Manu Jokela, Anna Sarkozy, Sushan Luo, Jordi Díaz-Manera,[...]. Genet Med 2020

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.
Sharie B Parks, Jessica D Kushner, Deirdre Nauman, Donna Burgess, Susan Ludwigsen, Amanda Peterson, Duanxiang Li, Petra Jakobs, Michael Litt, Charles B Porter,[...]. Am Heart J 2008

Sodium channel mutations and susceptibility to heart failure and atrial fibrillation.
Timothy M Olson, Virginia V Michels, Jeffrey D Ballew, Sandra P Reyna, Margaret L Karst, Kathleen J Herron, Steven C Horton, Richard J Rodeheffer, Jeffrey L Anderson. JAMA 2005

A Combined Linkage and Exome Sequencing Analysis for Electrocardiogram Parameters in the Erasmus Rucphen Family Study.
Claudia T Silva, Irina V Zorkoltseva, Najaf Amin, Ayşe Demirkan, Elisabeth M van Leeuwen, Jan A Kors, Marten van den Berg, Bruno H Stricker, André G Uitterlinden, Anatoly V Kirichenko,[...]. Front Genet 2016

Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience.
Karin Y van Spaendonck-Zwarts, Ingrid A W van Rijsingen, Maarten P van den Berg, Ronald H Lekanne Deprez, Jan G Post, Anneke M van Mil, Folkert W Asselbergs, Imke Christiaans, Irene M van Langen, Arthur A M Wilde,[...]. Eur J Heart Fail 2013

Peripartum cardiomyopathy as a part of familial dilated cardiomyopathy.
Karin Y van Spaendonck-Zwarts, J Peter van Tintelen, Dirk J van Veldhuisen, Rik van der Werf, Jan D H Jongbloed, Walter J Paulus, Dennis Dooijes, Maarten P van den Berg. Circulation 2010

Linkage analysis in the next-generation sequencing era.
Joan E Bailey-Wilson, Alexander F Wilson. Hum Hered 2011

Peripartum Cardiomyopathy: JACC State-of-the-Art Review.
Melinda B Davis, Zolt Arany, Dennis M McNamara, Sorel Goland, Uri Elkayam. J Am Coll Cardiol 2020

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.