A citation-based method for searching scientific literature

Bin Chen, MariBeth Gagnon, Shahram Shahangian, Nancy L Anderson, Devery A Howerton, Joe D Boone. MMWR Recomm Rep 2009
Times Cited: 55







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



Times Cited
  Times     Co-cited
Similarity


Developing a sustainable process to provide quality control materials for genetic testing.
Bin Chen, Catherine D O' Connell, D Joe Boone, Jean A Amos, Jeanne C Beck, Maria M Chan, Daniel H Farkas, Roger V Lebo, Carolyn Sue Richards, Benjamin B Roa,[...]. Genet Med 2005
34
29

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
508
14


Characterization of 107 genomic DNA reference materials for CYP2D6, CYP2C19, CYP2C9, VKORC1, and UGT1A1: a GeT-RM and Association for Molecular Pathology collaborative project.
Victoria M Pratt, Barbara Zehnbauer, Jean Amos Wilson, Ruth Baak, Nikolina Babic, Maria Bettinotti, Arlene Buller, Ken Butz, Matthew Campbell, Chris Civalier,[...]. J Mol Diagn 2010
64
12

A standardized framework for the validation and verification of clinical molecular genetic tests.
Christopher J Mattocks, Michael A Morris, Gert Matthijs, Elfriede Swinnen, Anniek Corveleyn, Els Dequeker, Clemens R Müller, Victoria Pratt, Andrew Wallace. Eur J Hum Genet 2010
104
12

Clinician perspectives about molecular genetic testing for heritable conditions and development of a clinician-friendly laboratory report.
Ira M Lubin, Margaret M McGovern, Zoe Gibson, Susan J Gross, Elaine Lyon, Roberta A Pagon, Victoria M Pratt, Jamila Rashid, Colleen Shaw, Lander Stoddard,[...]. J Mol Diagn 2009
30
20

A simple salting out procedure for extracting DNA from human nucleated cells.
S A Miller, D D Dykes, H F Polesky. Nucleic Acids Res 1988
10

Assuring the quality of next-generation sequencing in clinical laboratory practice.
Amy S Gargis, Lisa Kalman, Meredith W Berry, David P Bick, David P Dimmock, Tina Hambuch, Fei Lu, Elaine Lyon, Karl V Voelkerding, Barbara A Zehnbauer,[...]. Nat Biotechnol 2012
295
10

Quality control in molecular genetic testing.
E Dequeker, S Ramsden, W W Grody, T T Stenzel, D E Barton. Nat Rev Genet 2001
75
9

Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel.
Michael S Watson, Garry R Cutting, Robert J Desnick, Deborah A Driscoll, Katherine Klinger, Michael Mennuti, Glenn E Palomaki, Bradley W Popovich, Victoria M Pratt, Elizabeth M Rohlfs,[...]. Genet Med 2004
266
9

Ordering molecular genetic tests and reporting results: practices in laboratory and clinical settings.
Ira M Lubin, Michele Caggana, Carolyn Constantin, Susan J Gross, Elaine Lyon, Roberta A Pagon, Tracy L Trotter, Jean Amos Wilson, Margaret M McGovern. J Mol Diagn 2008
18
27

Report of an international survey of molecular genetic testing laboratories.
Margaret M McGovern, Rob Elles, Isabella Beretta, Martin J Somerville, Gerald Hoefler, Mauri Keinanen, David Barton, Nancy Carson, Elisabeth Dequeker, Radim Brdicka,[...]. Community Genet 2007
15
33

Establishment of stably EBV-transformed cell lines from residual clinical blood samples for use in performance evaluation and quality assurance in molecular genetic testing.
Susan H Bernacki, Ana K Stankovic, Laurina O Williams, Jeanne C Beck, James E Herndon, Karen Snow-Bailey, Thomas W Prior, Karla J Matteson, Linda M Wasserman, Eugene C Cole,[...]. J Mol Diagn 2003
27
14

Development of genomic reference materials for cystic fibrosis genetic testing.
Victoria M Pratt, Michele Caggana, Christina Bridges, Arlene M Buller, Lisa DiAntonio, W Edward Highsmith, Leonard M Holtegaard, Kasinathan Muralidharan, Elizabeth M Rohlfs, Jack Tarleton,[...]. J Mol Diagn 2009
24
16

Oversight of US genetic testing laboratories.
Kathy L Hudson, Juli A Murphy, David J Kaufman, Gail H Javitt, Sara H Katsanis, Joan Scott. Nat Biotechnol 2006
42
9

Monitoring standards for molecular genetic testing in the United Kingdom, the Netherlands, and Ireland.
Simon C Ramsden, Zandra Deans, David O Robinson, Roger Mountford, Erik A Sistermans, Wayne W Grody, Shirley McQuaid, Simon J Patton, Susan A R Stenhouse. Genet Test 2006
22
18

Quality assurance for Duchenne and Becker muscular dystrophy genetic testing: development of a genomic DNA reference material panel.
Lisa Kalman, Jay Leonard, Norman Gerry, Jack Tarleton, Christina Bridges, Julie M Gastier-Foster, Robert E Pyatt, Eileen Stonerock, Monique A Johnson, C Sue Richards,[...]. J Mol Diagn 2011
14
28

Recommended principles and practices for validating clinical molecular pathology tests.
Lawrence Jennings, Vivianna M Van Deerlin, Margaret L Gulley. Arch Pathol Lab Med 2009
113
7

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
7

A report template for molecular genetic tests designed to improve communication between the clinician and laboratory.
Maren T Scheuner, Lee Hilborne, Julie Brown, Ira M Lubin. Genet Test Mol Biomarkers 2012
23
17

Characterization of 137 Genomic DNA Reference Materials for 28 Pharmacogenetic Genes: A GeT-RM Collaborative Project.
Victoria M Pratt, Robin E Everts, Praful Aggarwal, Brittany N Beyer, Ulrich Broeckel, Ruth Epstein-Baak, Paul Hujsak, Ruth Kornreich, Jun Liao, Rachel Lorier,[...]. J Mol Diagn 2016
53
7

College of American Pathologists' laboratory standards for next-generation sequencing clinical tests.
Nazneen Aziz, Qin Zhao, Lynn Bry, Denise K Driscoll, Birgit Funke, Jane S Gibson, Wayne W Grody, Madhuri R Hegde, Gerald A Hoeltge, Debra G B Leonard,[...]. Arch Pathol Lab Med 2015
184
7

Evaluating the utility of personal genomic information.
Morris W Foster, John J Mulvihill, Richard R Sharp. Genet Med 2009
121
5


Successful transformation of cryopreserved lymphocytes: a resource for epidemiological studies.
J C Beck, C M Beiswanger, E M John, E Satariano, D West. Cancer Epidemiol Biomarkers Prev 2001
44
6

A novel method for creating artificial mutant samples for performance evaluation and quality control in clinical molecular genetics.
Michael Jarvis, Ramaswamy K Iyer, Laurina O Williams, Walter W Noll, Kirk Thomas, Milhan Telatar, Wayne W Grody. J Mol Diagn 2005
13
23

Quality assurance in molecular genetic testing laboratories.
M M McGovern, M O Benach, S Wallenstein, R J Desnick, R Keenlyside. JAMA 1999
48
6

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
499
5

Development of genomic reference materials for Huntington disease genetic testing.
Lisa Kalman, Monique A Johnson, Jeanne Beck, Elizabeth Berry-Kravis, Arlene Buller, Brett Casey, Gerald L Feldman, James Handsfield, John P Jakupciak, Samantha Maragh,[...]. Genet Med 2007
13
23

Consensus characterization of 16 FMR1 reference materials: a consortium study.
Jean Amos Wilson, Victoria M Pratt, Amit Phansalkar, Kasinathan Muralidharan, W Edward Highsmith, Jeanne C Beck, Scott Bridgeman, Ebony M Courtney, Lidia Epp, Andrea Ferreira-Gonzalez,[...]. J Mol Diagn 2008
30
10

The use and interpretation of commercial APC gene testing for familial adenomatous polyposis.
F M Giardiello, J D Brensinger, G M Petersen, M C Luce, L M Hylind, J A Bacon, S V Booker, R D Parker, S R Hamilton. N Engl J Med 1997
256
5

Frequency of problems during clinical molecular-genetic testing.
W T Hofgärtner, J F Tait. Am J Clin Pathol 1999
29
10

Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders--updated European recommendations.
Els Dequeker, Manfred Stuhrmann, Michael A Morris, Teresa Casals, Carlo Castellani, Mireille Claustres, Harry Cuppens, Marie des Georges, Claude Ferec, Milan Macek,[...]. Eur J Hum Genet 2009
141
5

Experience and outcome of 3 years of a European EQA scheme for genetic testing of the spinocerebellar ataxias.
Sara Seneca, Michael A Morris, Simon Patton, Rob Elles, Jorge Sequeiros. Eur J Hum Genet 2008
19
15

Alternative approaches to proficiency testing in molecular genetics.
C Sue Richards, Wayne W Grody. Clin Chem 2003
10
30

Effective communication of molecular genetic test results to primary care providers.
Maren T Scheuner, Maria Orlando Edelen, Lee H Hilborne, Ira M Lubin. Genet Med 2013
16
18


Clinical interpretation and implications of whole-genome sequencing.
Frederick E Dewey, Megan E Grove, Cuiping Pan, Benjamin A Goldstein, Jonathan A Bernstein, Hassan Chaib, Jason D Merker, Rachel L Goldfeder, Gregory M Enns, Sean P David,[...]. JAMA 2014
268
5


Preemptive clinical pharmacogenetics implementation: current programs in five US medical centers.
Henry M Dunnenberger, Kristine R Crews, James M Hoffman, Kelly E Caudle, Ulrich Broeckel, Scott C Howard, Robert J Hunkler, Teri E Klein, William E Evans, Mary V Relling. Annu Rev Pharmacol Toxicol 2015
234
5

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
5

Good laboratory practice for clinical next-generation sequencing informatics pipelines.
Amy S Gargis, Lisa Kalman, David P Bick, Cristina da Silva, David P Dimmock, Birgit H Funke, Sivakumar Gowrisankar, Madhuri R Hegde, Shashikant Kulkarni, Christopher E Mason,[...]. Nat Biotechnol 2015
80
5

Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls.
Justin M Zook, Brad Chapman, Jason Wang, David Mittelman, Oliver Hofmann, Winston Hide, Marc Salit. Nat Biotechnol 2014
400
5

Guidelines for diagnostic next-generation sequencing.
Gert Matthijs, Erika Souche, Mariëlle Alders, Anniek Corveleyn, Sebastian Eck, Ilse Feenstra, Valérie Race, Erik Sistermans, Marc Sturm, Marjan Weiss,[...]. Eur J Hum Genet 2016
212
5

Personal utility and genomic information: look before you leap.
Scott D Grosse, Colleen M McBride, James P Evans, Muin J Khoury. Genet Med 2009
52
3

Lamotrigine-induced common variable immune deficiency.
Julie Smith, Tus Fernando, Nicole McGrath, Rowan Ameratunga. Neurology 2004
23
8

Agammaglobulinemia.
O C BRUTON. Pediatrics 1952
866
3





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.