A citation-based method for searching scientific literature

Samuel J Aronson, Eugene H Clark, Matthew Varugheese, Samantha Baxter, Lawrence J Babb, Heidi L Rehm. Genet Med 2012
Times Cited: 70







List of co-cited articles
848 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
40

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
25

The GeneInsight Suite: a platform to support laboratory and provider use of DNA-based genetic testing.
Samuel J Aronson, Eugene H Clark, Lawrence J Babb, Samantha Baxter, Lisa M Farwell, Birgit H Funke, Amy Lovelette Hernandez, Victoria A Joshi, Elaine Lyon, Andrew R Parthum,[...]. Hum Mutat 2011
56
28

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007.
C Sue Richards, Sherri Bale, Daniel B Bellissimo, Soma Das, Wayne W Grody, Madhuri R Hegde, Elaine Lyon, Brian E Ward. Genet Med 2008
535
21

Technical desiderata for the integration of genomic data into Electronic Health Records.
Daniel R Masys, Gail P Jarvik, Neil F Abernethy, Nicholas R Anderson, George J Papanicolaou, Dina N Paltoo, Mark A Hoffman, Isaac S Kohane, Howard P Levy. J Biomed Inform 2012
65
18

Crossing the omic chasm: a time for omic ancillary systems.
Justin Starren, Marc S Williams, Erwin P Bottinger. JAMA 2013
54
20

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
15

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
511
14

Usability of a novel clinician interface for genetic results.
Pamela M Neri, Stephanie E Pollard, Lynn A Volk, Lisa P Newmark, Matthew Varugheese, Samantha Baxter, Samuel J Aronson, Heidi L Rehm, David W Bates. J Biomed Inform 2012
24
33

A systematic approach to assessing the clinical significance of genetic variants.
H Duzkale, J Shen, H McLaughlin, A Alfares, M A Kelly, T J Pugh, B H Funke, H L Rehm, M S Lebo. Clin Genet 2013
110
11

Genetic Misdiagnoses and the Potential for Health Disparities.
Arjun K Manrai, Birgit H Funke, Heidi L Rehm, Morten S Olesen, Bradley A Maron, Peter Szolovits, David M Margulies, Joseph Loscalzo, Isaac S Kohane. N Engl J Med 2016
320
11

The emerging role of the cardiac genetic counselor.
Jodie Ingles, Laura Yeates, Christopher Semsarian. Heart Rhythm 2011
72
10

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,[...]. Heart Rhythm 2011
619
10



The genome-enabled electronic medical record.
M A Hoffman. J Biomed Inform 2007
48
14

Electronic medical records and personalized medicine.
Mark A Hoffman, Marc S Williams. Hum Genet 2011
37
18

The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future.
Omri Gottesman, Helena Kuivaniemi, Gerard Tromp, W Andrew Faucett, Rongling Li, Teri A Manolio, Saskia C Sanderson, Joseph Kannry, Randi Zinberg, Melissa A Basford,[...]. Genet Med 2013
404
10

ClinVar: public archive of relationships among sequence variation and human phenotype.
Melissa J Landrum, Jennifer M Lee, George R Riley, Wonhee Jang, Wendy S Rubinstein, Deanna M Church, Donna R Maglott. Nucleic Acids Res 2014
10

Genetics of hypertrophic cardiomyopathy after 20 years: clinical perspectives.
Barry J Maron, Martin S Maron, Christopher Semsarian. J Am Coll Cardiol 2012
393
10

Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessment.
Jipin Das K, Jodie Ingles, Richard D Bagnall, Christopher Semsarian. Genet Med 2014
57
12

Points to consider in the reevaluation and reanalysis of genomic test results: a statement of the American College of Medical Genetics and Genomics (ACMG).
Joshua L Deignan, Wendy K Chung, Hutton M Kearney, Kristin G Monaghan, Catherine W Rehder, Elizabeth C Chao. Genet Med 2019
40
17

Patient re-contact after revision of genomic test results: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG).
Karen L David, Robert G Best, Leslie Manace Brenman, Lynn Bush, Joshua L Deignan, David Flannery, Jodi D Hoffman, Ingrid Holm, David T Miller, James O'Leary,[...]. Genet Med 2019
46
15

Clinical assessment incorporating a personal genome.
Euan A Ashley, Atul J Butte, Matthew T Wheeler, Rong Chen, Teri E Klein, Frederick E Dewey, Joel T Dudley, Kelly E Ormond, Aleksandra Pavlovic, Alexander A Morgan,[...]. Lancet 2010
464
8


Opportunities for genomic clinical decision support interventions.
Casey Lynnette Overby, Isaac Kohane, Joseph L Kannry, Marc S Williams, Justin Starren, Erwin Bottinger, Omri Gottesman, Joshua C Denny, Chunhua Weng, Peter Tarczy-Hornoch,[...]. Genet Med 2013
41
14


A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record.
Peter Tarczy-Hornoch, Laura Amendola, Samuel J Aronson, Levi Garraway, Stacy Gray, Robert W Grundmeier, Lucia A Hindorff, Gail Jarvik, Dean Karavite, Matthew Lebo,[...]. Genet Med 2013
48
12

A novel clinician interface to improve clinician access to up-to-date genetic results.
Allison R Wilcox, Pamela M Neri, Lynn A Volk, Lisa P Newmark, Eugene H Clark, Lawrence J Babb, Matthew Varugheese, Samuel J Aronson, Heidi L Rehm, David W Bates. J Am Med Inform Assoc 2014
13
46

Practical challenges in integrating genomic data into the electronic health record.
Abel N Kho, Luke V Rasmussen, John J Connolly, Peggy L Peissig, Justin Starren, Hakon Hakonarson, M Geoffrey Hayes. Genet Med 2013
46
13

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.
Bryony A Thompson, Amanda B Spurdle, John-Paul Plazzer, Marc S Greenblatt, Kiwamu Akagi, Fahd Al-Mulla, Bharati Bapat, Inge Bernstein, Gabriel Capellá, Johan T den Dunnen,[...]. Nat Genet 2014
304
8

Shared genetic causes of cardiac hypertrophy in children and adults.
Hiroyuki Morita, Heidi L Rehm, Andres Menesses, Barbara McDonough, Amy E Roberts, Raju Kucherlapati, Jeffrey A Towbin, J G Seidman, Christine E Seidman. N Engl J Med 2008
252
8

ACMG clinical laboratory standards for next-generation sequencing.
Heidi L Rehm, Sherri J Bale, Pinar Bayrak-Toydemir, Jonathan S Berg, Kerry K Brown, Joshua L Deignan, Michael J Friez, Birgit H Funke, Madhuri R Hegde, Elaine Lyon. Genet Med 2013
535
8

Clinical predictors of genetic testing outcomes in hypertrophic cardiomyopathy.
Jodie Ingles, Tanya Sarina, Laura Yeates, Lauren Hunt, Ivan Macciocca, Louise McCormack, Ingrid Winship, Julie McGaughran, John Atherton, Christopher Semsarian. Genet Med 2013
72
8

Penetrance of hypertrophic cardiomyopathy in children and adolescents: a 12-year follow-up study of clinical screening and predictive genetic testing.
Morten K Jensen, Ole Havndrup, Michael Christiansen, Paal S Andersen, Birgitte Diness, Anna Axelsson, Flemming Skovby, Lars Køber, Henning Bundgaard. Circulation 2013
71
8

Natural history of genotype positive-phenotype negative patients with hypertrophic cardiomyopathy.
Belinda Gray, Jodie Ingles, Christopher Semsarian. Int J Cardiol 2011
48
12

Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases.
Philippe Charron, Michael Arad, Eloisa Arbustini, Cristina Basso, Zofia Bilinska, Perry Elliott, Tiina Helio, Andre Keren, William J McKenna, Lorenzo Monserrat,[...]. Eur Heart J 2010
253
8

Risk of Cardiomyopathy in Younger Persons With a Family History of Death from Cardiomyopathy: A Nationwide Family Study in a Cohort of 3.9 Million Persons.
Mattis F Ranthe, Lisbeth Carstensen, Nina Øyen, Morten K Jensen, Anna Axelsson, Jan Wohlfahrt, Mads Melbye, Henning Bundgaard, Heather A Boyd. Circulation 2015
12
50

Clinical laboratories collaborate to resolve differences in variant interpretations submitted to ClinVar.
Steven M Harrison, Jill S Dolinsky, Amy E Knight Johnson, Tina Pesaran, Danielle R Azzariti, Sherri Bale, Elizabeth C Chao, Soma Das, Lisa Vincent, Heidi L Rehm. Genet Med 2017
123
8

Hypertrophic cardiomyopathy: present and future, with translation into contemporary cardiovascular medicine.
Barry J Maron, Steve R Ommen, Christopher Semsarian, Paolo Spirito, Iacopo Olivotto, Martin S Maron. J Am Coll Cardiol 2014
364
8

Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity.
Ahmed A Alfares, Melissa A Kelly, Gregory McDermott, Birgit H Funke, Matthew S Lebo, Samantha B Baxter, Jun Shen, Heather M McLaughlin, Eugene H Clark, Larry J Babb,[...]. Genet Med 2015
213
8

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
134
8

Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics.
Daniele Carrieri, Heidi C Howard, Caroline Benjamin, Angus J Clarke, Sandi Dheensa, Shane Doheny, Naomi Hawkins, Tanya F Halbersma-Konings, Leigh Jackson, Hülya Kayserili,[...]. Eur J Hum Genet 2019
35
17

Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy.
Daniel M Jordan, Adam Kiezun, Samantha M Baxter, Vineeta Agarwala, Robert C Green, Michael F Murray, Trevor Pugh, Matthew S Lebo, Heidi L Rehm, Birgit H Funke,[...]. Am J Hum Genet 2011
49
10

Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units.
Carol Jean Saunders, Neil Andrew Miller, Sarah Elizabeth Soden, Darrell Lee Dinwiddie, Aaron Noll, Noor Abu Alnadi, Nevene Andraws, Melanie LeAnn Patterson, Lisa Ann Krivohlavek, Joel Fellis,[...]. Sci Transl Med 2012
375
7

Communicating genetic risk information for common disorders in the era of genomic medicine.
Denise M Lautenbach, Kurt D Christensen, Jeffrey A Sparks, Robert C Green. Annu Rev Genomics Hum Genet 2013
84
7

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
7


Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results.
Sharon E Plon, Diana M Eccles, Douglas Easton, William D Foulkes, Maurizio Genuardi, Marc S Greenblatt, Frans B L Hogervorst, Nicoline Hoogerbrugge, Amanda B Spurdle, Sean V Tavtigian. Hum Mutat 2008
560
7



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.