A citation-based method for searching scientific literature

Michael R Sargen, Donato Calista, David E Elder, Daniela Massi, Emily Y Chu, Míriam Potrony, Ruth M Pfeiffer, Cristina Carrera, Paula Aguilera, Llucia Alos, Susana Puig, Rosalie Elenitsas, Xiaohong R Yang, Margaret A Tucker, Maria Teresa Landi, Alisa M Goldstein. J Am Acad Dermatol 2020
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Germline mutations in shelterin complex genes are associated with familial glioma.
Matthew N Bainbridge, Georgina N Armstrong, M Monica Gramatges, Alison A Bertuch, Shalini N Jhangiani, Harsha Doddapaneni, Lora Lewis, Joseph Tombrello, Spyros Tsavachidis, Yanhong Liu,[...]. J Natl Cancer Inst 2014
130
100

Germline mutations in BAP1 predispose to melanocytic tumors.
Thomas Wiesner, Anna C Obenauf, Rajmohan Murali, Isabella Fried, Klaus G Griewank, Peter Ulz, Christian Windpassinger, Werner Wackernagel, Shea Loy, Ingrid Wolf,[...]. Nat Genet 2011
452
100

Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers.
Mohamed H Abdel-Rahman, Robert Pilarski, Colleen M Cebulla, James B Massengill, Benjamin N Christopher, Getachew Boru, Peter Hovland, Frederick H Davidorf. J Med Genet 2011
293
100

POT1 loss-of-function variants predispose to familial melanoma.
Carla Daniela Robles-Espinoza, Mark Harland, Andrew J Ramsay, Lauren G Aoude, Víctor Quesada, Zhihao Ding, Karen A Pooley, Antonia L Pritchard, Jessamy C Tiffen, Mia Petljak,[...]. Nat Genet 2014
217
100

Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer.
Daniel Chubb, Peter Broderick, Sara E Dobbins, Matthew Frampton, Ben Kinnersley, Steven Penegar, Amy Price, Yussanne P Ma, Amy L Sherborne, Claire Palles,[...]. Nat Commun 2016
83
100

The Medical Genome Reference Bank contains whole genome and phenotype data of 2570 healthy elderly.
Mark Pinese, Paul Lacaze, Emma M Rath, Andrew Stone, Marie-Jo Brion, Adam Ameur, Sini Nagpal, Clare Puttick, Shane Husson, Dmitry Degrave,[...]. Nat Commun 2020
17
50

Comprehensive Study of the Clinical Phenotype of Germline BAP1 Variant-Carrying Families Worldwide.
Sebastian Walpole, Antonia L Pritchard, Colleen M Cebulla, Robert Pilarski, Meredith Stautberg, Frederick H Davidorf, Arnaud de la Fouchardière, Odile Cabaret, Lisa Golmard, Dominique Stoppa-Lyonnet,[...]. J Natl Cancer Inst 2018
80
50

The wide spectrum of POT1 gene variants correlates with multiple cancer types.
Oriol Calvete, Pablo Garcia-Pavia, Fernando Domínguez, Gaelle Bougeard, Kristin Kunze, Andreas Braeuninger, Alex Teule, Adriana Lasa, Teresa Ramón Y Cajal, Gemma Llort,[...]. Eur J Hum Genet 2017
35
50

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
50

Melanoma genetics.
Jazlyn Read, Karin A W Wadt, Nicholas K Hayward. J Med Genet 2016
110
50

Germline mutations in candidate predisposition genes in individuals with cutaneous melanoma and at least two independent additional primary cancers.
Antonia L Pritchard, Peter A Johansson, Vaishnavi Nathan, Madeleine Howlie, Judith Symmons, Jane M Palmer, Nicholas K Hayward. PLoS One 2018
9
50

Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma.
Lisa Mirabello, Bin Zhu, Roelof Koster, Eric Karlins, Michael Dean, Meredith Yeager, Matthew Gianferante, Logan G Spector, Lindsay M Morton, Danielle Karyadi,[...]. JAMA Oncol 2020
48
50

Pathogenic Germline Variants in 10,389 Adult Cancers.
Kuan-Lin Huang, R Jay Mashl, Yige Wu, Deborah I Ritter, Jiayin Wang, Clara Oh, Marta Paczkowska, Sheila Reynolds, Matthew A Wyczalkowski, Ninad Oak,[...]. Cell 2018
278
50

Frequent Mutations of POT1 Distinguish Pulmonary Sarcomatoid Carcinoma From Other Lung Cancer Histologies.
Erica Shen, Joanne Xiu, Rex Bentley, Giselle Y López, Kyle M Walsh. Clin Lung Cancer 2020
2
50

Germline mutations in Protection of Telomeres 1 in two families with Hodgkin lymphoma.
Mary L McMaster, Chongkui Sun, Maria T Landi, Sharon A Savage, Melissa Rotunno, Xiaohong R Yang, Kristine Jones, Aurélie Vogt, Amy Hutchinson, Bin Zhu,[...]. Br J Haematol 2018
21
50

Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma.
Jianxin Shi, Xiaohong R Yang, Bari Ballew, Melissa Rotunno, Donato Calista, Maria Concetta Fargnoli, Paola Ghiorzo, Brigitte Bressac-de Paillerets, Eduardo Nagore, Marie Francoise Avril,[...]. Nat Genet 2014
198
50

MC1R germline variants confer risk for BRAF-mutant melanoma.
Maria Teresa Landi, Jürgen Bauer, Ruth M Pfeiffer, David E Elder, Benjamin Hulley, Paola Minghetti, Donato Calista, Peter A Kanetsky, Daniel Pinkel, Boris C Bastian. Science 2006
236
50

Prevalence of germline BAP1 mutation in a population-based sample of uveal melanoma cases.
Lauren G Aoude, Claire M Vajdic, Anne Kricker, Bruce Armstrong, Nicholas K Hayward. Pigment Cell Melanoma Res 2013
43
50

Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls.
Darren R Brenner, Paul Brennan, Paolo Boffetta, Christopher I Amos, Margaret R Spitz, Chu Chen, Gary Goodman, Joachim Heinrich, Heike Bickeböller, Albert Rosenberger,[...]. Hum Genet 2013
26
50

Risk of non-melanoma cancers in first-degree relatives of CDKN2A mutation carriers.
Bhramar Mukherjee, John Oliver Delancey, Leon Raskin, Jessica Everett, Joanne Jeter, Colin B Begg, Irene Orlow, Marianne Berwick, Bruce K Armstrong, Anne Kricker,[...]. J Natl Cancer Inst 2012
30
50

A new POT1 germline mutation-expanding the spectrum of POT1-associated cancers.
Tremika Le-Shan Wilson, Namita Hattangady, Antonio Marcondes Lerario, Carmen Williams, Erika Koeppe, Shane Quinonez, Jenae Osborne, Kelly B Cha, Tobias Else. Fam Cancer 2017
21
50

Dermoscopy comparative approach for early diagnosis in familial melanoma: influence of MC1R genotype.
C Longo, V Barquet, E Hernandez, A A Marghoob, M Potrony, C Carrera, P Aguilera, C Badenas, J Malvehy, S Puig. J Eur Acad Dermatol Venereol 2021
3
50

Hereditary uveal melanoma: a report of a germline mutation in BAP1.
Veronica Höiom, Daniel Edsgärd, Hildur Helgadottir, Hanna Eriksson, Charlotta All-Ericsson, Rainer Tuominen, Ivayla Ivanova, Joakim Lundeberg, Olof Emanuelsson, Johan Hansson. Genes Chromosomes Cancer 2013
39
50

Sex and MC1R variants in human pigmentation: Differences in tanning ability and sensitivity to sunlight between sexes.
Barbara Hernando, Maider Ibarrola-Villava, Maria Peña-Chilet, Santos Alonso, Gloria Ribas, Conrado Martinez-Cadenas. J Dermatol Sci 2016
8
50

BAP1 and cancer.
Michele Carbone, Haining Yang, Harvey I Pass, Thomas Krausz, Joseph R Testa, Giovanni Gaudino. Nat Rev Cancer 2013
367
50

Germline BAP1 inactivation is preferentially associated with metastatic ocular melanoma and cutaneous-ocular melanoma families.
Ching-Ni Jenny Njauw, Ivana Kim, Adriano Piris, Michele Gabree, Michael Taylor, Anne Marie Lane, Margaret M DeAngelis, Evangelos Gragoudas, Lyn M Duncan, Hensin Tsao. PLoS One 2012
168
50

Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposure.
E Matichard, P Verpillat, R Meziani, B Gérard, V Descamps, E Legroux, M Burnouf, G Bertrand, F Bouscarat, A Archimbaud,[...]. J Med Genet 2004
103
50

Genetic epidemiology of cutaneous melanoma: a global perspective.
A M Goldstein, M A Tucker. Arch Dermatol 2001
79
50


Genome-wide analysis of noncoding regulatory mutations in cancer.
Nils Weinhold, Anders Jacobsen, Nikolaus Schultz, Chris Sander, William Lee. Nat Genet 2014
316
50

The melanocortin-1-receptor gene is the major freckle gene.
M Bastiaens, J ter Huurne, N Gruis, W Bergman, R Westendorp, B J Vermeer, J N Bouwes Bavinck. Hum Mol Genet 2001
132
50

Genotype-phenotype relationships in U.S. melanoma-prone families with CDKN2A and CDK4 mutations.
A M Goldstein, J P Struewing, A Chidambaram, M C Fraser, M A Tucker. J Natl Cancer Inst 2000
133
50

High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL.
Alisa M Goldstein, May Chan, Mark Harland, Elizabeth M Gillanders, Nicholas K Hayward, Marie-Francoise Avril, Esther Azizi, Giovanna Bianchi-Scarra, D Timothy Bishop, Brigitte Bressac-de Paillerets,[...]. Cancer Res 2006
273
50

A cryptic BAP1 splice mutation in a family with uveal and cutaneous melanoma, and paraganglioma.
Karin Wadt, Jiyeon Choi, Joon-Yong Chung, Jens Kiilgaard, Steffen Heegaard, Krzysztof T Drzewiecki, Jeffrey M Trent, Stephen M Hewitt, Nicholas K Hayward, Anne-Marie Gerdes,[...]. Pigment Cell Melanoma Res 2012
83
50

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
Anubha Mahajan, Min Jin Go, Weihua Zhang, Jennifer E Below, Kyle J Gaulton, Teresa Ferreira, Momoko Horikoshi, Andrew D Johnson, Maggie C Y Ng, Inga Prokopenko,[...]. Nat Genet 2014
668
50

Biologically distinct subsets of nevi.
Tova Rogers, Maria L Marino, Patricia Raciti, Manu Jain, Klaus J Busam, Michael A Marchetti, Ashfaq A Marghoob. G Ital Dermatol Venereol 2016
11
50

A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.
Helen E Speedy, Maria Chiara Di Bernardo, Georgina P Sava, Martin J S Dyer, Amy Holroyd, Yufei Wang, Nicola J Sunter, Larry Mansouri, Gunnar Juliusson, Karin E Smedby,[...]. Nat Genet 2014
124
50

High risk of tobacco-related cancers in CDKN2A mutation-positive melanoma families.
Hildur Helgadottir, Veronica Höiom, Göran Jönsson, Rainer Tuominen, Christian Ingvar, Ake Borg, Håkan Olsson, Johan Hansson. J Med Genet 2014
48
50

Genotypic and Phenotypic Features of BAP1 Cancer Syndrome: A Report of 8 New Families and Review of Cases in the Literature.
Alexandra M Haugh, Ching-Ni Njauw, Jeffrey A Bubley, Anna Elisa Verzì, Bin Zhang, Emily Kudalkar, Timothy VandenBoom, Kara Walton, Brian L Swick, Raj Kumar,[...]. JAMA Dermatol 2017
45
50

Common 5p15.33 and 6p21.33 variants influence lung cancer risk.
Yufei Wang, Peter Broderick, Emily Webb, Xifeng Wu, Jayaram Vijayakrishnan, Athena Matakidou, Mobshra Qureshi, Qiong Dong, Xiangjun Gu, Wei Vivien Chen,[...]. Nat Genet 2008
424
50

Clinical, pathological and dermoscopic phenotype of MITF p.E318K carrier cutaneous melanoma patients.
Giulia Ciccarese, Bruna Dalmasso, William Bruno, Paola Queirolo, Lorenza Pastorino, Virginia Andreotti, Francesco Spagnolo, Enrica Tanda, Giovanni Ponti, Cesare Massone,[...]. J Transl Med 2020
9
50

Variants in or near KITLG, BAK1, DMRT1, and TERT-CLPTM1L predispose to familial testicular germ cell tumour.
Christian P Kratz, Summer S Han, Philip S Rosenberg, Sonja I Berndt, Laurie Burdett, Meredith Yeager, Larissa A Korde, Phuong L Mai, Ruth Pfeiffer, Mark H Greene. J Med Genet 2011
62
50

Germline BAP1 mutations also predispose to cutaneous squamous cell carcinoma.
Robert V Rawson, Geoffrey F Watson, Annabelle M Maher, Stanley W McCarthy, John F Thompson, Richard A Scolyer. Pathology 2017
10
50

Melanocortin 1 receptor (MC1R) variants in high melanoma risk patients are associated with specific dermoscopic ABCD features.
Koen D Quint, Jasper I van der Rhee, Nelleke A Gruis, Jeanet A Ter Huurne, Ron Wolterbeek, Nienke van der Stoep, Wilma Bergman, Nicole A Kukutsch. Acta Derm Venereol 2012
15
50

Development of a high risk pancreatic screening clinic using 3.0 T MRI.
Chad A Barnes, Elizabeth Krzywda, Shannon Lahiff, Dena McDowell, Kathleen K Christians, Paul Knechtges, Parag Tolat, Mark Hohenwalter, Kulwinder Dua, Abdul H Khan,[...]. Fam Cancer 2018
9
50


Characterization of melanoma susceptibility genes in high-risk patients from Central Italy.
Cristina Pellegrini, Maria Giovanna Maturo, Claudia Martorelli, Mariano Suppa, Ambra Antonini, Dimitra Kostaki, Lucilla Verna, Maria Teresa Landi, Ketty Peris, Maria Concetta Fargnoli. Melanoma Res 2017
20
50

Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom.
Mark Harland, Anne E Cust, Celia Badenas, Yu-Mei Chang, Elizabeth A Holland, Paula Aguilera, Joanne F Aitken, Bruce K Armstrong, Jennifer H Barrett, Cristina Carrera,[...]. Hered Cancer Clin Pract 2014
25
50

CDKN2A and MC1R variants influence dermoscopic and confocal features of benign melanocytic lesions in multiple melanoma patients.
Sara Bassoli, Andrea Maurichi, Monica Rodolfo, Alice Casari, Simona Frigerio, Gaia Pupelli, Francesca Farnetani, Giuseppe Pelosi, Mario Santinami, Giovanni Pellacani. Exp Dermatol 2013
22
50

Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?
J S Palmer, D L Duffy, N F Box, J F Aitken, L E O'Gorman, A C Green, N K Hayward, N G Martin, R A Sturm. Am J Hum Genet 2000
384
50


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.