A citation-based method for searching scientific literature

Kenki Matsumoto, Derek Lim, Paul D Pharoah, Eamonn R Maher, Stefan J Marciniak. Eur J Hum Genet 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Colorectal cancer risk in families with Birt-Hogg-Dubé syndrome increased.
Elke C Sattler, Zulfiya Syunyaeva, Marlene Reithmair, Wolfram Dempke, Ortrud K Steinlein. Eur J Cancer 2021
3
66

A comparison of genotyping arrays.
Joost A M Verlouw, Eva Clemens, Jard H de Vries, Oliver Zolk, Annemieke J M H Verkerk, Antoinette Am Zehnhoff-Dinnesen, Carolina Medina-Gomez, Claudia Lanvers-Kaminsky, Fernando Rivadeneira, Thorsten Langer,[...]. Eur J Hum Genet 2021
5
33

Stakeholders' views of integrating universal tumour screening and genetic testing for colorectal and endometrial cancer into routine oncology.
Rosie O'Shea, Nicole M Rankin, Maira Kentwell, Margaret Gleeson, Katherine M Tucker, Heather Hampel, Natalie Taylor, Sarah Lewis. Eur J Hum Genet 2021
1
100

TAB2 deletions and variants cause a highly recognisable syndrome with mitral valve disease, cardiomyopathy, short stature and hypermobility.
Aafke Engwerda, Erika K S M Leenders, Barbara Frentz, Paulien A Terhal, Katharina Löhner, Bert B A de Vries, Trijnie Dijkhuizen, Yvonne J Vos, Tuula Rinne, Maarten P van den Berg,[...]. Eur J Hum Genet 2021
5
33

The genetic structure of Norway.
Morten Mattingsdal, S Sunna Ebenesersdóttir, Kristjan H S Moore, Ole A Andreassen, Thomas F Hansen, Thomas Werge, Ingrid Kockum, Tomas Olsson, Lars Alfredsson, Agnar Helgason,[...]. Eur J Hum Genet 2021
3
33

SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect.
Alisdair McNeill, Emanuela Iovino, Luke Mansard, Christel Vache, David Baux, Emma Bedoukian, Helen Cox, John Dean, David Goudie, Ajith Kumar,[...]. Brain 2020
16
33

Identifying challenges in neurofibromatosis: a modified Delphi procedure.
Britt A E Dhaenens, Rosalie E Ferner, Annette Bakker, Marco Nievo, D Gareth Evans, Pierre Wolkenstein, Cornelia Potratz, Scott R Plotkin, Guenter Heimann, Eric Legius,[...]. Eur J Hum Genet 2021
1
100

Deletion in COL4A2 is associated with a three-generation variable phenotype: from fetal to adult manifestations.
Moran Hausman-Kedem, Liat Ben-Sira, Debora Kidron, Shay Ben-Shachar, Rachel Straussberg, Daphna Marom, Penina Ponger, Anat Bar-Shira, Gustavo Malinger, Aviva Fattal-Valevski. Eur J Hum Genet 2021
2
50

Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability.
Natja Haag, Ene-Choo Tan, Matthias Begemann, Lars Buschmann, Florian Kraft, Petra Holschbach, Angeline H M Lai, Maggie Brett, Ganeshwaran H Mochida, Stephanie DiTroia,[...]. Eur J Hum Genet 2021
3
33

The FNIP co-chaperones decelerate the Hsp90 chaperone cycle and enhance drug binding.
Mark R Woodford, Diana M Dunn, Adam R Blanden, Dante Capriotti, David Loiselle, Chrisostomos Prodromou, Barry Panaretou, Philip F Hughes, Aaron Smith, Wendi Ackerman,[...]. Nat Commun 2016
36
33

High frequency of somatic frameshift BHD gene mutations in Birt-Hogg-Dubé-associated renal tumors.
Cathy D Vocke, Youfeng Yang, Christian P Pavlovich, Laura S Schmidt, Michael L Nickerson, Carlos A Torres-Cabala, Maria J Merino, McClellan M Walther, Berton Zbar, W Marston Linehan. J Natl Cancer Inst 2005
159
33

Blood and lymphatic systems are segregated by the FLCN tumor suppressor.
Ikue Tai-Nagara, Yukiko Hasumi, Dai Kusumoto, Hisashi Hasumi, Keisuke Okabe, Tomofumi Ando, Fumio Matsuzaki, Fumiko Itoh, Hideyuki Saya, Chang Liu,[...]. Nat Commun 2020
6
33

Folliculin (Flcn) inactivation leads to murine cardiac hypertrophy through mTORC1 deregulation.
Yukiko Hasumi, Masaya Baba, Hisashi Hasumi, Ying Huang, Martin Lang, Rachel Reindorf, Hyoung-bin Oh, Sebastiano Sciarretta, Kunio Nagashima, Diana C Haines,[...]. Hum Mol Genet 2014
37
33

Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome.
Michael L Nickerson, Michelle B Warren, Jorge R Toro, Vera Matrosova, Gladys Glenn, Maria L Turner, Paul Duray, Maria Merino, Peter Choyke, Christian P Pavlovich,[...]. Cancer Cell 2002
609
33

Lung cysts, spontaneous pneumothorax, and genetic associations in 89 families with Birt-Hogg-Dubé syndrome.
Jorge R Toro, Stephen E Pautler, Laveta Stewart, Gladys M Glenn, Michael Weinreich, Ousmane Toure, Ming-Hui Wei, Laura S Schmidt, Lewis Davis, Berton Zbar,[...]. Am J Respir Crit Care Med 2007
200
33

H255Y and K508R missense mutations in tumour suppressor folliculin (FLCN) promote kidney cell proliferation.
Hisashi Hasumi, Yukiko Hasumi, Masaya Baba, Hafumi Nishi, Mitsuko Furuya, Cathy D Vocke, Martin Lang, Nobuko Irie, Chiharu Esumi, Maria J Merino,[...]. Hum Mol Genet 2017
13
33

The tumor suppressor folliculin inhibits lactate dehydrogenase A and regulates the Warburg effect.
Mark R Woodford, Alexander J Baker-Williams, Rebecca A Sager, Sarah J Backe, Adam R Blanden, Fiza Hashmi, Priyanka Kancherla, Alessandro Gori, David R Loiselle, Matteo Castelli,[...]. Nat Struct Mol Biol 2021
2
50

Kidney-targeted Birt-Hogg-Dube gene inactivation in a mouse model: Erk1/2 and Akt-mTOR activation, cell hyperproliferation, and polycystic kidneys.
Masaya Baba, Mutsuo Furihata, Seung-Beom Hong, Lino Tessarollo, Diana C Haines, Eileen Southon, Vishal Patel, Peter Igarashi, W Gregory Alvord, Robert Leighty,[...]. J Natl Cancer Inst 2008
172
33

Folliculin-interacting proteins Fnip1 and Fnip2 play critical roles in kidney tumor suppression in cooperation with Flcn.
Hisashi Hasumi, Masaya Baba, Yukiko Hasumi, Martin Lang, Ying Huang, HyoungBin F Oh, Masayuki Matsuo, Maria J Merino, Masahiro Yao, Yusuke Ito,[...]. Proc Natl Acad Sci U S A 2015
50
33

TSC2 regulates lysosome biogenesis via a non-canonical RAGC and TFEB-dependent mechanism.
Nicola Alesi, Elie W Akl, Damir Khabibullin, Heng-Jia Liu, Anna S Nidhiry, Emma R Garner, Harilaos Filippakis, Hilaire C Lam, Wei Shi, Srinivas R Viswanathan,[...]. Nat Commun 2021
8
33

Risk of renal and colonic neoplasms and spontaneous pneumothorax in the Birt-Hogg-Dubé syndrome.
Berton Zbar, W Gregory Alvord, Gladys Glenn, Maria Turner, Christian P Pavlovich, Laura Schmidt, McClellan Walther, Peter Choyke, Gregor Weirich, Stephen M Hewitt,[...]. Cancer Epidemiol Biomarkers Prev 2002
350
33

Topical rapamycin as a treatment for fibrofolliculomas in Birt-Hogg-Dubé syndrome: a double-blind placebo-controlled randomized split-face trial.
Lieke M C Gijezen, Marigje Vernooij, Herm Martens, Charlene E U Oduber, Charles J M Henquet, Theo M Starink, Martin H Prins, Fred H Menko, Patty J Nelemans, Maurice A M van Steensel. PLoS One 2014
23
33

Birt-Hogg-Dubé syndrome: a novel marker of kidney neoplasia.
J R Toro, G Glenn, P Duray, T Darling, G Weirich, B Zbar, M Linehan, M L Turner. Arch Dermatol 1999
251
33

Transcriptional activation of RagD GTPase controls mTORC1 and promotes cancer growth.
Chiara Di Malta, Diletta Siciliano, Alessia Calcagni, Jlenia Monfregola, Simona Punzi, Nunzia Pastore, Andrea N Eastes, Oliver Davis, Rossella De Cegli, Angela Zampelli,[...]. Science 2017
106
33

Evaluation and management of renal tumors in the Birt-Hogg-Dubé syndrome.
Christian P Pavlovich, Robert L Grubb, Kathleen Hurley, Gladys M Glenn, Jorge Toro, Laura S Schmidt, Carlos Torres-Cabala, Maria J Merino, Berton Zbar, Peter Choyke,[...]. J Urol 2005
168
33

Homozygous loss of BHD causes early embryonic lethality and kidney tumor development with activation of mTORC1 and mTORC2.
Yukiko Hasumi, Masaya Baba, Rieko Ajima, Hisashi Hasumi, Vladimir A Valera, Mara E Klein, Diana C Haines, Maria J Merino, Seung-Beom Hong, Terry P Yamaguchi,[...]. Proc Natl Acad Sci U S A 2009
164
33

Tumor suppressor Tsc1 is a new Hsp90 co-chaperone that facilitates folding of kinase and non-kinase clients.
Mark R Woodford, Rebecca A Sager, Elijah Marris, Diana M Dunn, Adam R Blanden, Ryan L Murphy, Nicholas Rensing, Oleg Shapiro, Barry Panaretou, Chrisostomos Prodromou,[...]. EMBO J 2017
40
33


Prevalence of Birt-Hogg-Dubé Syndrome Determined Through Epidemiological Data on Spontaneous Pneumothorax and Bayes Theorem.
Marie-Eve Muller, Cécile Daccord, Patrick Taffé, Romain Lazor. Front Med (Lausanne) 2021
3
33

Clinical and genetic spectrum of Birt-Hogg-Dube syndrome patients in whom pneumothorax and/or multiple lung cysts are the presenting feature.
Makiko Kunogi, Masatoshi Kurihara, Takako Shigihara Ikegami, Toshiyuki Kobayashi, Noriko Shindo, Toshio Kumasaka, Yoko Gunji, Mika Kikkawa, Shin-ichiro Iwakami, Okio Hino,[...]. J Med Genet 2010
93
33

Negative regulation of EGFR signalling by the human folliculin tumour suppressor protein.
Laura A Laviolette, Julien Mermoud, Isabel A Calvo, Nicholas Olson, Myriam Boukhali, Ortrud K Steinlein, Elisabeth Roider, Elke C Sattler, Dachuan Huang, Bin Tean Teh,[...]. Nat Commun 2017
25
33

The folliculin-FNIP1 pathway deleted in human Birt-Hogg-Dubé syndrome is required for murine B-cell development.
Masaya Baba, Jonathan R Keller, Hong-Wei Sun, Wolfgang Resch, Stefan Kuchen, Hyung Chan Suh, Hisashi Hasumi, Yukiko Hasumi, Kyong-Rim Kieffer-Kwon, Carme Gallego Gonzalez,[...]. Blood 2012
50
33

Sporadic renal angiomyolipoma in a patient with Birt-Hogg-Dubé: chaperones in pathogenesis.
Rebecca A Sager, Mark R Woodford, Oleg Shapiro, Mehdi Mollapour, Gennady Bratslavsky. Oncotarget 2018
7
33

Inactivation of the FLCN tumor suppressor gene induces TFE3 transcriptional activity by increasing its nuclear localization.
Seung-Beom Hong, HyoungBin Oh, Vladimir A Valera, Masaya Baba, Laura S Schmidt, W Marston Linehan. PLoS One 2010
97
33

Novel mutations in the BHD gene and absence of loss of heterozygosity in fibrofolliculomas of Birt-Hogg-Dubé patients.
Maurice A M van Steensel, Valerie L R M Verstraeten, Jorge Frank, Nicole W J Kelleners-Smeets, Pamela Poblete-Gutiérrez, Dominique Marcus-Soekarman, Reno S Bladergroen, Peter M Steijlen, Michel van Geel. J Invest Dermatol 2007
57
33

A Total Pleural Covering for Lymphangioleiomyomatosis Prevents Pneumothorax Recurrence.
Masatoshi Kurihara, Teruaki Mizobuchi, Hideyuki Kataoka, Teruhiko Sato, Toshio Kumasaka, Hiroki Ebana, Sumitaka Yamanaka, Reina Endo, Sumika Miyahashira, Noriko Shinya,[...]. PLoS One 2016
24
33

A substrate-specific mTORC1 pathway underlies Birt-Hogg-Dubé syndrome.
Gennaro Napolitano, Chiara Di Malta, Alessandra Esposito, Mariana E G de Araujo, Salvatore Pece, Giovanni Bertalot, Maria Matarese, Valerio Benedetti, Angela Zampelli, Taras Stasyk,[...]. Nature 2020
70
33

Mesenchymal folliculin is required for alveolar development: implications for cystic lung disease in Birt-Hogg-Dubé syndrome.
Ling Chu, Yongfeng Luo, Hui Chen, Qing Miao, Larry Wang, Rex Moats, Tiansheng Wang, John C Kennedy, Elizabeth P Henske, Wei Shi. Thorax 2020
5
33

Renal Cell Carcinoma in Tuberous Sclerosis Complex.
Elizabeth P Henske, Kristine M Cornejo, Chin-Lee Wu. Genes (Basel) 2021
3
33

Regulation of mitochondrial oxidative metabolism by tumor suppressor FLCN.
Hisashi Hasumi, Masaya Baba, Yukiko Hasumi, Ying Huang, Hyoungbin Oh, Robert M Hughes, Mara E Klein, Shoichi Takikita, Kunio Nagashima, Laura S Schmidt,[...]. J Natl Cancer Inst 2012
61
33

Renal tumors in the Birt-Hogg-Dubé syndrome.
Christian P Pavlovich, McClellan M Walther, Robin A Eyler, Stephen M Hewitt, Berton Zbar, W Marston Linehan, Maria J Merino. Am J Surg Pathol 2002
368
33

The tumor suppressor folliculin regulates AMPK-dependent metabolic transformation.
Ming Yan, Marie-Claude Gingras, Elaine A Dunlop, Yann Nouët, Fanny Dupuy, Zahra Jalali, Elite Possik, Barry J Coull, Dmitri Kharitidi, Anders Bondo Dydensborg,[...]. J Clin Invest 2014
100
33

A total pleural covering of absorbable cellulose mesh prevents pneumothorax recurrence in patients with Birt-Hogg-Dubé syndrome.
Teruaki Mizobuchi, Masatoshi Kurihara, Hiroki Ebana, Sumitaka Yamanaka, Hideyuki Kataoka, Shouichi Okamoto, Etsuko Kobayashi, Toshio Kumasaka, Kuniaki Seyama. Orphanet J Rare Dis 2018
7
33

Loss of FLCN-FNIP1/2 induces a non-canonical interferon response in human renal tubular epithelial cells.
Iris E Glykofridis, Jaco C Knol, Jesper A Balk, Denise Westland, Thang V Pham, Sander R Piersma, Sinéad M Lougheed, Sepide Derakhshan, Puck Veen, Martin A Rooimans,[...]. Elife 2021
4
33

Absence of the Birt-Hogg-Dubé gene product is associated with increased hypoxia-inducible factor transcriptional activity and a loss of metabolic flexibility.
R S Preston, A Philp, T Claessens, L Gijezen, A B Dydensborg, E A Dunlop, K T Harper, T Brinkhuizen, F H Menko, D M Davies,[...]. Oncogene 2011
52
33

Folliculin encoded by the BHD gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling.
Masaya Baba, Seung-Beom Hong, Nirmala Sharma, Michelle B Warren, Michael L Nickerson, Akihiro Iwamatsu, Dominic Esposito, William K Gillette, Ralph F Hopkins, James L Hartley,[...]. Proc Natl Acad Sci U S A 2006
330
33

A FLCN-TFE3 Feedback Loop Prevents Excessive Glycogenesis and Phagocyte Activation by Regulating Lysosome Activity.
Mitsuhiro Endoh, Masaya Baba, Tamie Endoh, Akiyoshi Hirayama, Ayako Nakamura-Ishizu, Terumasa Umemoto, Michihiro Hashimoto, Kunio Nagashima, Tomoyoshi Soga, Martin Lang,[...]. Cell Rep 2020
11
33

Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (FamCan-NGS).
Marta Ramírez-Calvo, Zaida García-Casado, Antonio Fernández-Serra, Inmaculada de Juan, Sarai Palanca, Silvestre Oltra, José Luis Soto, Adela Castillejo, Víctor M Barbera, Ma José Juan-Fita,[...]. Hered Cancer Clin Pract 2019
8
33


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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.