A citation-based method for searching scientific literature

Jeffrey N Weitzel, Veronica I Lagos, Carey A Cullinane, Patricia J Gambol, Julie O Culver, Kathleen R Blazer, Melanie R Palomares, Katrina J Lowstuter, Deborah J MacDonald. JAMA 2007
Times Cited: 130







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



Times Cited
  Times     Co-cited
Similarity


Evaluation of the contribution of germline variants in BRCA1 and BRCA2 to uveal and cutaneous melanoma.
Peter A Johansson, Vaishnavi Nathan, Lauren M Bourke, Jane M Palmer, Tongwu Zhang, Judith Symmons, Madeleine Howlie, Ann-Marie Patch, Jazlyn Read, Elizabeth A Holland,[...]. Melanoma Res 2019
6
16

Evaluating clinician acceptability of the prototype CanRisk tool for predicting risk of breast and ovarian cancer: A multi-methods study.
Stephanie Archer, Chantal Babb de Villiers, Fiona Scheibl, Tim Carver, Simon Hartley, Andrew Lee, Alex P Cunningham, Douglas F Easton, Jennifer G McIntosh, Jon Emery,[...]. PLoS One 2020
13
7


Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer.
Colin C Pritchard, Joaquin Mateo, Michael F Walsh, Navonil De Sarkar, Wassim Abida, Himisha Beltran, Andrea Garofalo, Roman Gulati, Suzanne Carreira, Rosalind Eeles,[...]. N Engl J Med 2016
699
1

SIFT: Predicting amino acid changes that affect protein function.
Pauline C Ng, Steven Henikoff. Nucleic Acids Res 2003
1

Gastroenteropancreatic neuroendocrine neoplasms: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up.
M Pavel, K Öberg, M Falconi, E P Krenning, A Sundin, A Perren, A Berruti. Ann Oncol 2020
116
1

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
2

Adrenocortical carcinoma.
Tobias Else, Alex C Kim, Aaron Sabolch, Victoria M Raymond, Asha Kandathil, Elaine M Caoili, Shruti Jolly, Barbra S Miller, Thomas J Giordano, Gary D Hammer. Endocr Rev 2014
404
1

Medical genomics: The intricate path from genetic variant identification to clinical interpretation.
B Quintáns, A Ordóñez-Ugalde, P Cacheiro, A Carracedo, M J Sobrido. Appl Transl Genom 2014
22
4

Omics for personalized medicine: defining the current we swim in.
Rania Ibrahim, Maria Pasic, George M Yousef. Expert Rev Mol Diagn 2016
20
5

Genetics of parathyroid tumours.
R V Thakker. J Intern Med 2016
47
2

Utility of chromogranin A, pancreatic polypeptide, glucagon and gastrin in the diagnosis and follow-up of pancreatic neuroendocrine tumours in multiple endocrine neoplasia type 1 patients.
Wei Qiu, Ioannis Christakis, Angelica Silva, Roland L Bassett, Liyun Cao, Qing H Meng, Elizabeth Gardner Grubbs, Hua Zhao, James C Yao, Jeffrey E Lee,[...]. Clin Endocrinol (Oxf) 2016
26
3

Clinical Interpretation of Genomic Variations.
Müge Sayitoğlu. Turk J Haematol 2016
5
20

GENETICS IN ENDOCRINOLOGY: Genetic diagnosis of endocrine diseases by NGS: novel scenarios and unpredictable results and risks.
Luca Persani, Tiziana de Filippis, Carla Colombo, Davide Gentilini. Eur J Endocrinol 2018
10
10

Next-generation diagnostics: gene panel, exome, or whole genome?
Yu Sun, Claudia A L Ruivenkamp, Mariëtte J V Hoffer, Terry Vrijenhoek, Marjolein Kriek, Christi J van Asperen, Johan T den Dunnen, Gijs W E Santen. Hum Mutat 2015
83
1

Adrenocortical carcinomas and malignant phaeochromocytomas: ESMO-EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up.
M Fassnacht, G Assie, E Baudin, G Eisenhofer, C de la Fouchardiere, H R Haak, R de Krijger, F Porpiglia, M Terzolo, A Berruti. Ann Oncol 2020
53
1

Clinical exome sequencing for genetic identification of rare Mendelian disorders.
Hane Lee, Joshua L Deignan, Naghmeh Dorrani, Samuel P Strom, Sibel Kantarci, Fabiola Quintero-Rivera, Kingshuk Das, Traci Toy, Bret Harry, Michael Yourshaw,[...]. JAMA 2014
567
1

True MEN1 or phenocopy? Evidence for geno-phenotypic correlations in MEN1 syndrome.
Annamária Kövesdi, Miklós Tóth, Henriett Butz, Nikolette Szücs, Beatrix Sármán, Péter Pusztai, Judit Tőke, Péter Reismann, Mónika Fáklya, Géza Tóth,[...]. Endocrine 2019
8
12



Nephron-sparing surgery for multifocal and hereditary renal tumors.
Adam R Metwalli, William M Linehan. Curr Opin Urol 2014
23
4

Classification and Clinical Management of Variants of Uncertain Significance in High Penetrance Cancer Predisposition Genes.
Setareh Moghadasi, Diana M Eccles, Peter Devilee, Maaike P G Vreeswijk, Christi J van Asperen. Hum Mutat 2016
17
5


Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN).
Thomas Eggermann, Miriam Elbracht, Ingo Kurth, Anders Juul, Trine Holm Johannsen, Irène Netchine, George Mastorakos, Gudmundur Johannsson, Thomas J Musholt, Martin Zenker,[...]. Orphanet J Rare Dis 2020
7
14



Thyroid cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up†.
S Filetti, C Durante, D Hartl, S Leboulleux, L D Locati, K Newbold, M G Papotti, A Berruti. Ann Oncol 2019
142
1

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
236
1

Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care.
S L Sawyer, T Hartley, D A Dyment, C L Beaulieu, J Schwartzentruber, A Smith, H M Bedford, G Bernard, F P Bernier, B Brais,[...]. Clin Genet 2016
206
1

The Genetics of Pituitary Adenomas.
Christina Tatsi, Constantine A Stratakis. J Clin Med 2019
13
7

Genetic counselling and testing of susceptibility genes for therapeutic decision-making in breast cancer-an European consensus statement and expert recommendations.
Christian F Singer, Judith Balmaña, Nicole Bürki, Suzette Delaloge, Maria Elisabetta Filieri, Anna-Marie Gerdes, Eli Marie Grindedal, Sileni Han, Oskar Johansson, Bella Kaufman,[...]. Eur J Cancer 2019
7
14


Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes.
Vassily Trubetskoy, Alex Rodriguez, Uptal Dave, Nicholas Campbell, Emily L Crawford, Edwin H Cook, James S Sutcliffe, Ian Foster, Ravi Madduri, Nancy J Cox,[...]. Bioinformatics 2015
10
10


Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes.
James Whitworth, Philip S Smith, Jose-Ezequiel Martin, Hannah West, Andrea Luchetti, Faye Rodger, Graeme Clark, Keren Carss, Jonathan Stephens, Kathleen Stirrups,[...]. Am J Hum Genet 2018
26
3

Comparative analysis of algorithms for next-generation sequencing read alignment.
Matthew Ruffalo, Thomas LaFramboise, Mehmet Koyutürk. Bioinformatics 2011
119
1


A Clinical Roadmap to Investigate the Genetic Basis of Pediatric Pheochromocytoma: Which Genes Should Physicians Think About?
Bernardo Dias Pereira, Tiago Nunes da Silva, Ana Teresa Bernardo, Rui César, Henrique Vara Luiz, Karel Pacak, Luísa Mota-Vieira. Int J Endocrinol 2018
7
14


Genetic testing in endocrine surgery: Opportunities for precision surgery.
Wilson Alobuia, Justin Annes, Electron Kebebew. Surgery 2020
4
25

Next-generation sequencing in the clinical genetic screening of patients with pheochromocytoma and paraganglioma.
Joakim Crona, Alberto Delgado Verdugo, Dan Granberg, Staffan Welin, Peter Stålberg, Per Hellman, Peyman Björklund. Endocr Connect 2013
36
2

When should genetic testing be performed in patients with neuroendocrine tumours?
Triona O'Shea, Maralyn Druce. Rev Endocr Metab Disord 2017
12
8


Bioinformatics for clinical next generation sequencing.
Gavin R Oliver, Steven N Hart, Eric W Klee. Clin Chem 2015
58
1

Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma.
Samuel A Wells, Sylvia L Asa, Henning Dralle, Rossella Elisei, Douglas B Evans, Robert F Gagel, Nancy Lee, Andreas Machens, Jeffrey F Moley, Furio Pacini,[...]. Thyroid 2015
837
1

Evaluation and comparison of multiple aligners for next-generation sequencing data analysis.
Jing Shang, Fei Zhu, Wanwipa Vongsangnak, Yifei Tang, Wenyu Zhang, Bairong Shen. Biomed Res Int 2014
28
3

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
1


Molecular genetic testing and the future of clinical genomics.
Sara Huston Katsanis, Nicholas Katsanis. Nat Rev Genet 2013
210
1

Next-generation sequencing approach for the diagnosis of human diseases: open challenges and new opportunities.
Chiara Di Resta, Silvia Galbiati, Paola Carrera, Maurizio Ferrari. EJIFCC 2018
41
2


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.