A citation-based method for searching scientific literature

Sanne W Ten Broeke, Mar Rodríguez-Girondo, Manon Suerink, Stefan Aretz, Inge Bernstein, Gabriel Capellá, Christoph Engel, Encarna B Gomez-Garcia, Liselot P van Hest, Magnus von Knebel Doeberitz, Kristina Lagerstedt-Robinson, Tom G W Letteboer, Pal Moller, Theo A van Os, Marta Pineda, Nils Rahner, Maran J W Olderode-Berends, Jenny von Salomé, Hans K Schackert, Liesbeth Spruijt, Verena Steinke-Lange, Anja Wagner, Carli M J Tops, Maartje Nielsen. Cancer Epidemiol Biomarkers Prev 2019
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Genetic anticipation in Swedish Lynch syndrome families.
Jenny von Salomé, Philip S Boonstra, Masoud Karimi, Gustav Silander, Marie Stenmark-Askmalm, Samuel Gebre-Medhin, Christos Aravidis, Mef Nilbert, Annika Lindblom, Kristina Lagerstedt-Robinson. PLoS Genet 2017
9
100

Disease anticipation is associated with progressive telomere shortening in families with dyskeratosis congenita due to mutations in TERC.
Tom Vulliamy, Anna Marrone, Richard Szydlo, Amanda Walne, Philip J Mason, Inderjeet Dokal. Nat Genet 2004
326
66

Anticipation in lynch syndrome: where we are where we go.
Cristina Bozzao, Patrizia Lastella, Alessandro Stella. Curr Genomics 2011
17
66


Anticipation: an old idea in new genes.
M G McInnis. Am J Hum Genet 1996
92
33

Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1).
Rajesh V Thakker, Paul J Newey, Gerard V Walls, John Bilezikian, Henning Dralle, Peter R Ebeling, Shlomo Melmed, Akihiro Sakurai, Francesco Tonelli, Maria Luisa Brandi. J Clin Endocrinol Metab 2012
647
33

'Quality in, quality out', a stepwise approach to EBM for rare diseases promoted by MEN1.
Dirk-Jan van Beek, Rachel S van Leeuwaarde, Carolina Rc Pieterman, Menno R Vriens, Gerlof D Valk. Endocr Connect 2018
11
33

Genetic anticipation is associated with telomere shortening in hereditary breast cancer.
Beatriz Martinez-Delgado, Kira Yanowsky, Lucia Inglada-Perez, Samuel Domingo, Miguel Urioste, Ana Osorio, Javier Benitez. PLoS Genet 2011
71
33

Ascertainment bias causes false signal of anticipation in genetic prion disease.
Eric Vallabh Minikel, Inga Zerr, Steven J Collins, Claudia Ponto, Alison Boyd, Genevieve Klug, André Karch, Joanna Kenny, John Collinge, Leonel T Takada,[...]. Am J Hum Genet 2014
27
33

Intra-Familial Phenotypic Heterogeneity and Telomere Abnormality in von Hippel- Lindau Disease: Implications for Personalized Surveillance Plan and Pathogenesis of VHL-Associated Tumors.
Jiangyi Wang, Xiang Peng, Cen Chen, Xianghui Ning, Shuanghe Peng, Teng Li, Shengjie Liu, Baoan Hong, Jingcheng Zhou, Kaifang Ma,[...]. Front Genet 2019
4
33

Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome.
Adam Shlien, Uri Tabori, Christian R Marshall, Malgorzata Pienkowska, Lars Feuk, Ana Novokmet, Sonia Nanda, Harriet Druker, Stephen W Scherer, David Malkin. Proc Natl Acad Sci U S A 2008
139
33

Evidence for genetic anticipation in vonHippel-Lindau syndrome.
Laura Aronoff, David Malkin, Kalene van Engelen, Bailey Gallinger, Jonathan Wasserman, Raymond H Kim, Anita Villani, M Stephen Meyn, Harriet Druker. J Med Genet 2018
8
33

Unraveling the intrafamilial correlations and heritability of tumor types in MEN1: a Groupe d'étude des Tumeurs Endocrines study.
J Thevenon, A Bourredjem, L Faivre, C Cardot-Bauters, A Calender, M Le Bras, S Giraud, P Niccoli, M F Odou, F Borson-Chazot,[...]. Eur J Endocrinol 2015
20
33

Younger age of cancer initiation is associated with shorter telomere length in Li-Fraumeni syndrome.
Uri Tabori, Sonia Nanda, Harriet Druker, Jodi Lees, David Malkin. Cancer Res 2007
104
33

A review of statistical methods for testing genetic anticipation: looking for an answer in Lynch syndrome.
Philip S Boonstra, Stephen B Gruber, Victoria M Raymond, Shu-Chen Huang, Susanne Timshel, Mef Nilbert, Bhramar Mukherjee. Genet Epidemiol 2010
26
33

Risk factors and causes of death in MEN1 disease. A GTE (Groupe d'Etude des Tumeurs Endocrines) cohort study among 758 patients.
Pierre Goudet, Arnaud Murat, Christine Binquet, Christine Cardot-Bauters, Annie Costa, Philippe Ruszniewski, Patricia Niccoli, Fabrice Ménégaux, Georges Chabrier, Françoise Borson-Chazot,[...]. World J Surg 2010
189
33

Acromegaly in a multiple endocrine neoplasia type 1 (MEN1) family with low penetrance of the disease.
Koen M A Dreijerink, André P van Beek, Eef G W M Lentjes, Jan G Post, Rob B van der Luijt, Marijke R Canninga-van Dijk, Cornelis J M Lips. Eur J Endocrinol 2005
12
33

MEN1 redefined, a clinical comparison of mutation-positive and mutation-negative patients.
Joanne M de Laat, Rob B van der Luijt, Carolina R C Pieterman, Maria P Oostveen, Ad R Hermus, Olaf M Dekkers, Wouter W de Herder, Anouk N van der Horst-Schrivers, Madeleine L Drent, Peter H Bisschop,[...]. BMC Med 2016
55
33

Twenty years of menin: emerging opportunities for restoration of transcriptional regulation in MEN1.
Koen M A Dreijerink, H T Marc Timmers, Myles Brown. Endocr Relat Cancer 2017
30
33

Competing risk analysis using R: an easy guide for clinicians.
L Scrucca, A Santucci, F Aversa. Bone Marrow Transplant 2007
471
33

Care for patients with multiple endocrine neoplasia type 1: the current evidence base.
C R C Pieterman, M R Vriens, K M A Dreijerink, R B van der Luijt, G D Valk. Fam Cancer 2011
27
33

Is there anticipation in the age at onset of cancer in families with Li-Fraumeni syndrome?
Marie Trkova, Marie Hladikova, Pavel Kasal, Petr Goetz, Zdenek Sedlacek. J Hum Genet 2002
34
33

The future: medical advances in MEN1 therapeutic approaches and management strategies.
Rachel S van Leeuwaarde, Joanne M de Laat, Carolina R C Pieterman, Koen Dreijerink, Menno R Vriens, Gerlof D Valk. Endocr Relat Cancer 2017
12
33

The association of telomere length and genetic variation in telomere biology genes.
Lisa Mirabello, Kai Yu, Peter Kraft, Immaculata De Vivo, David J Hunter, Jennifer Prescott, Jason Y Y Wong, Nilanjan Chatterjee, Richard B Hayes, Sharon A Savage. Hum Mutat 2010
84
33


Expanded repeat sequences and disease.
K Lindblad, M Schalling. Semin Neurol 1999
24
33

Genetic anticipation in BRCA1/BRCA2 families after controlling for ascertainment bias and cohort effect.
Rodrigo Santa Cruz Guindalini, Andrew Song, James D Fackenthal, Olufunmilayo I Olopade, Dezheng Huo. Cancer 2016
11
33

Regression modeling of competing risk using R: an in depth guide for clinicians.
L Scrucca, A Santucci, F Aversa. Bone Marrow Transplant 2010
310
33

Positional cloning of the gene for multiple endocrine neoplasia-type 1.
S C Chandrasekharappa, S C Guru, P Manickam, S E Olufemi, F S Collins, M R Emmert-Buck, L V Debelenko, Z Zhuang, I A Lubensky, L A Liotta,[...]. Science 1997
33

Whole-genome sequencing analysis of phenotypic heterogeneity and anticipation in Li-Fraumeni cancer predisposition syndrome.
Hany Ariffin, Pierre Hainaut, Anna Puzio-Kuter, Soo Sin Choong, Adelyne Sue Li Chan, Denis Tolkunov, Gunaretnam Rajagopal, Wenfeng Kang, Leon Li Wen Lim, Shekhar Krishnan,[...]. Proc Natl Acad Sci U S A 2014
19
33

A large multiple endocrine neoplasia type 1 family with clinical expression suggestive of anticipation.
S Giraud, H Choplin, B T Teh, J Lespinasse, A Jouvet, F Labat-Moleur, G Lenoir, B Hamon, P Hamon, A Calender. J Clin Endocrinol Metab 1997
62
33

Do patients with multiple endocrine neoplasia syndrome type 1 benefit from periodical screening?
Engelien A M Geerdink, Rob B Van der Luijt, Cornelis J M Lips. Eur J Endocrinol 2003
57
33

Cell biology of disease: Telomeropathies: an emerging spectrum disorder.
Brody Holohan, Woodring E Wright, Jerry W Shay. J Cell Biol 2014
113
33

Identification of seven loci affecting mean telomere length and their association with disease.
Veryan Codd, Christopher P Nelson, Eva Albrecht, Massimo Mangino, Joris Deelen, Jessica L Buxton, Jouke Jan Hottenga, Krista Fischer, Tõnu Esko, Ida Surakka,[...]. Nat Genet 2013
616
33

Mismatch repair gene deficiency and genetic anticipation in Lynch syndrome: myth or reality?
Giovanni Ponti, Cristel Ruini, Aldo Tomasi. Dis Colon Rectum 2015
6
33

Assessing how reduced expression levels of the mismatch repair genes MLH1, MSH2, and MSH6 affect repair efficiency.
Minttu Kansikas, Mariann Kasela, Jukka Kantelinen, Minna Nyström. Hum Mutat 2014
17
33

Longitudinal versus cross-sectional evaluations of leukocyte telomere length dynamics: age-dependent telomere shortening is the rule.
W Chen, M Kimura, S Kim, X Cao, S R Srinivasan, G S Berenson, J D Kark, A Aviv. J Gerontol A Biol Sci Med Sci 2011
155
33

The short and long telomere syndromes: paired paradigms for molecular medicine.
Susan E Stanley, Mary Armanios. Curr Opin Genet Dev 2015
76
33

Evidence for alternative lengthening of telomeres in liposarcomas in the absence of ALT-associated PML bodies.
Jennie N Jeyapalan, Aaron Mendez-Bermudez, Nadia Zaffaroni, Yuri E Dubrova, Nicola J Royle. Int J Cancer 2008
42
33



Microsatellite instability in the peripheral blood leukocytes of HNPCC patients.
Mary I Coolbaugh-Murphy, Jing-Ping Xu, Louis S Ramagli, Brian C Ramagli, Barry W Brown, Patrick M Lynch, Stanley R Hamilton, Marsha L Frazier, Michael J Siciliano. Hum Mutat 2010
22
33

Telomere length and genetic anticipation in Lynch syndrome.
Nuria Seguí, Marta Pineda, Elisabet Guinó, Ester Borràs, Matilde Navarro, Fernando Bellido, Victor Moreno, Conxi Lázaro, Ignacio Blanco, Gabriel Capellá,[...]. PLoS One 2013
18
33


Comparison of telomere length measurement methods.
Tsung-Po Lai, Woodring E Wright, Jerry W Shay. Philos Trans R Soc Lond B Biol Sci 2018
97
33


Telomere Length Maintenance and Its Transcriptional Regulation in Lynch Syndrome and Sporadic Colorectal Carcinoma.
Lilit Nersisyan, Lydia Hopp, Henry Loeffler-Wirth, Jörg Galle, Markus Loeffler, Arsen Arakelyan, Hans Binder. Front Oncol 2019
16
33

Human telomeres that contain (CTAGGG)n repeats show replication dependent instability in somatic cells and the male germline.
Aaron Mendez-Bermudez, Mark Hills, Hilda A Pickett, Anh Tuân Phan, Jean-Louis Mergny, Jean-François Riou, Nicola J Royle. Nucleic Acids Res 2009
27
33

Shelterin-Mediated Telomere Protection.
Titia de Lange. Annu Rev Genet 2018
279
33

Low levels of microsatellite instability characterize MLH1 and MSH2 HNPCC carriers before tumor diagnosis.
Hafid Alazzouzi, Enric Domingo, Sara González, Ignacio Blanco, Manel Armengol, Eloi Espín, Alberto Plaja, Simó Schwartz, Gabriel Capella, Simó Schwartz. Hum Mol Genet 2005
37
33


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.