A citation-based method for searching scientific literature

Tess D Pottinger, Megan J Puckelwartz, Lorenzo L Pesce, Avery Robinson, Samuel Kearns, Jennifer A Pacheco, Laura J Rasmussen-Torvik, Maureen E Smith, Rex Chisholm, Elizabeth M McNally. J Am Heart Assoc 2020
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


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
100

Truncations of titin causing dilated cardiomyopathy.
Daniel S Herman, Lien Lam, Matthew R G Taylor, Libin Wang, Polakit Teekakirikul, Danos Christodoulou, Lauren Conner, Steven R DePalma, Barbara McDonough, Elizabeth Sparks,[...]. N Engl J Med 2012
713
42

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
799
42

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
35
42


The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing.
Trevor J Pugh, Melissa A Kelly, Sivakumar Gowrisankar, Elizabeth Hynes, Michael A Seidman, Samantha M Baxter, Mark Bowser, Bryan Harrison, Daniel Aaron, Lisa M Mahanta,[...]. Genet Med 2014
179
42

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
42

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
149
28

Population-based variation in cardiomyopathy genes.
Jessica R Golbus, Megan J Puckelwartz, John P Fahrenbach, Lisa M Dellefave-Castillo, Don Wolfgeher, Elizabeth M McNally. Circ Cardiovasc Genet 2012
104
28

Precision Medicine in the Management of Dilated Cardiomyopathy: JACC State-of-the-Art Review.
Diane Fatkin, Inken G Huttner, Jason C Kovacic, J G Seidman, Christine E Seidman. J Am Coll Cardiol 2019
21
28

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
28

Evolution and functional impact of rare coding variation from deep sequencing of human exomes.
Jacob A Tennessen, Abigail W Bigham, Timothy D O'Connor, Wenqing Fu, Eimear E Kenny, Simon Gravel, Sean McGee, Ron Do, Xiaoming Liu, Goo Jun,[...]. Science 2012
28

Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome.
Najim Lahrouchi, Hariharan Raju, Elisabeth M Lodder, Efstathios Papatheodorou, James S Ware, Michael Papadakis, Rafik Tadros, Della Cole, Jonathan R Skinner, Jackie Crawford,[...]. J Am Coll Cardiol 2017
105
28

HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013.
Silvia G Priori, Arthur A Wilde, Minoru Horie, Yongkeun Cho, Elijah R Behr, Charles Berul, Nico Blom, Josep Brugada, Chern-En Chiang, Heikki Huikuri,[...]. Heart Rhythm 2013
978
28

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
129
28

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
122
28

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
41
28

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
28

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
144
28

Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy.
Francesco Mazzarotto, Upasana Tayal, Rachel J Buchan, William Midwinter, Alicja Wilk, Nicola Whiffin, Risha Govind, Erica Mazaika, Antonio de Marvao, Timothy J W Dawes,[...]. Circulation 2020
49
28

2012 ACCF/AHA/HRS focused update incorporated into the ACCF/AHA/HRS 2008 guidelines for device-based therapy of cardiac rhythm abnormalities: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines and the Heart Rhythm Society.
Andrew E Epstein, John P DiMarco, Kenneth A Ellenbogen, N A Mark Estes, Roger A Freedman, Leonard S Gettes, A Marc Gillinov, Gabriel Gregoratos, Stephen C Hammill, David L Hayes,[...]. J Am Coll Cardiol 2013
554
28

Rare variant mutations in pregnancy-associated or peripartum cardiomyopathy.
Ana Morales, Thomas Painter, Ran Li, Jill D Siegfried, Duanxiang Li, Nadine Norton, Ray E Hershberger. Circulation 2010
124
28

Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
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. Genet Med 2018
68
28

ClinGen--the Clinical Genome Resource.
Heidi L Rehm, Jonathan S Berg, Lisa D Brooks, Carlos D Bustamante, James P Evans, Melissa J Landrum, David H Ledbetter, Donna R Maglott, Christa Lese Martin, Robert L Nussbaum,[...]. N Engl J Med 2015
482
28

A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy.
Benjamin Meder, Frank Rühle, Tanja Weis, Georg Homuth, Andreas Keller, Jennifer Franke, Barbara Peil, Justo Lorenzo Bermejo, Karen Frese, Andreas Huge,[...]. Eur Heart J 2014
81
28

Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathy.
Katharine M Brauch, Margaret L Karst, Kathleen J Herron, Mariza de Andrade, Patricia A Pellikka, Richard J Rodeheffer, Virginia V Michels, Timothy M Olson. J Am Coll Cardiol 2009
200
28

Dilated cardiomyopathy: the complexity of a diverse genetic architecture.
Ray E Hershberger, Dale J Hedges, Ana Morales. Nat Rev Cardiol 2013
435
28

A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.
Eric Villard, Claire Perret, Françoise Gary, Carole Proust, Gilles Dilanian, Christian Hengstenberg, Volker Ruppert, Eloisa Arbustini, Thomas Wichter, Marine Germain,[...]. Eur Heart J 2011
195
28

A Genome-Wide Association Study of Idiopathic Dilated Cardiomyopathy in African Americans.
Huichun Xu, Gerald W Dorn, Amol Shetty, Ankita Parihar, Tushar Dave, Shawn W Robinson, Stephen S Gottlieb, Mark P Donahue, Gordon F Tomaselli, William E Kraus,[...]. J Pers Med 2018
17
28

Atlas of the clinical genetics of human dilated cardiomyopathy.
Jan Haas, Karen S Frese, Barbara Peil, Wanda Kloos, Andreas Keller, Rouven Nietsch, Zhu Feng, Sabine Müller, Elham Kayvanpour, Britta Vogel,[...]. Eur Heart J 2015
288
28

Variant Interpretation for Dilated Cardiomyopathy: Refinement of the American College of Medical Genetics and Genomics/ClinGen Guidelines for the DCM Precision Medicine Study.
Ana Morales, Daniel D Kinnamon, Elizabeth Jordan, Julia Platt, Matteo Vatta, Michael O Dorschner, Carl A Starkey, Jonathan O Mead, Tomohiko Ai, Wylie Burke,[...]. Circ Genom Precis Med 2020
16
28

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
326
28

ClinVar at five years: Delivering on the promise.
Melissa J Landrum, Brandi L Kattman. Hum Mutat 2018
66
14

Points to consider for laboratories reporting results from diagnostic genomic sequencing.
D F Vears, K Sénécal, A J Clarke, L Jackson, A M Laberge, L Lovrecic, A Piton, K L I Van Gassen, H G Yntema, B M Knoppers,[...]. Eur J Hum Genet 2018
28
14

Health and population effects of rare gene knockouts in adult humans with related parents.
Vagheesh M Narasimhan, Karen A Hunt, Dan Mason, Christopher L Baker, Konrad J Karczewski, Michael R Barnes, Anthony H Barnett, Chris Bates, Srikanth Bellary, Nicholas A Bockett,[...]. Science 2016
143
14

A systematic survey of loss-of-function variants in human protein-coding genes.
Daniel G MacArthur, Suganthi Balasubramanian, Adam Frankish, Ni Huang, James Morris, Klaudia Walter, Luke Jostins, Lukas Habegger, Joseph K Pickrell, Stephen B Montgomery,[...]. Science 2012
751
14

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).
Michael J Ackerman, Silvia G Priori, Stephan Willems, Charles Berul, Ramon Brugada, Hugh Calkins, A John Camm, Patrick T Ellinor, Michael Gollob, Robert Hamilton,[...]. Europace 2011
450
14

Variants of Uncertain Significance and "Missing Pathogenicity".
Diane Fatkin, Renee Johnson. J Am Heart Assoc 2020
4
25

Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era.
Nadine Norton, Peggy D Robertson, Mark J Rieder, Stephan Züchner, Evadnie Rampersaud, Eden Martin, Duanxiang Li, Deborah A Nickerson, Ray E Hershberger. Circ Cardiovasc Genet 2012
98
14

Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms.
Danya F Vears, Emilia Niemiec, Heidi Carmen Howard, Pascal Borry. Eur J Hum Genet 2018
28
14

Proof of "disease causing" mutation.
R G Cotton, C R Scriver. Hum Mutat 1998
148
14


A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation.
A A Geisterfer-Lowrance, S Kass, G Tanigawa, H P Vosberg, W McKenna, C E Seidman, J G Seidman. Cell 1990
957
14


ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
14

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.
Sara L Van Driest, Quinn S Wells, Sarah Stallings, William S Bush, Adam Gordon, Deborah A Nickerson, Jerry H Kim, David R Crosslin, Gail P Jarvik, David S Carrell,[...]. JAMA 2016
113
14

Prospective Study of Cancer Genetic Variants: Variation in Rate of Reclassification by Ancestry.
Thomas P Slavin, Lily R Van Tongeren, Carolyn E Behrendt, Ilana Solomon, Christina Rybak, Bita Nehoray, Lili Kuzmich, Mariana Niell-Swiller, Kathleen R Blazer, Shu Tao,[...]. J Natl Cancer Inst 2018
19
14


Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group.
Richard R Fabsitz, Amy McGuire, Richard R Sharp, Mona Puggal, Laura M Beskow, Leslie G Biesecker, Ebony Bookman, Wylie Burke, Esteban Gonzalez Burchard, George Church,[...]. Circ Cardiovasc Genet 2010
280
14

Complexities of Genetic Testing in Familial Dilated Cardiomyopathy.
Matthew J Wolf, Dagny Noeth, Chidambaram Rammohan, Svati H Shah. Circ Cardiovasc Genet 2016
4
25


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.