A citation-based method for searching scientific literature

M Tassabehji, V E Newton, A P Read. Nat Genet 1994
Times Cited: 515







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



Times Cited
  Times     Co-cited
Similarity


Review and update of mutations causing Waardenburg syndrome.
Véronique Pingault, Dorothée Ente, Florence Dastot-Le Moal, Michel Goossens, Sandrine Marlin, Nadège Bondurand. Hum Mutat 2010
346
36

Waardenburg syndrome.
A P Read, V E Newton. J Med Genet 1997
359
33

SLUG (SNAI2) deletions in patients with Waardenburg disease.
Manuel Sánchez-Martín, Arancha Rodríguez-García, Jesús Pérez-Losada, Ana Sagrera, Andrew P Read, Isidro Sánchez-García. Hum Mol Genet 2002
160
33

Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein.
C A Hodgkinson, K J Moore, A Nakayama, E Steingrímsson, N G Copeland, N A Jenkins, H Arnheiter. Cell 1993
903
30

Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4.
Nadege Bondurand, Florence Dastot-Le Moal, Laure Stanchina, Nathalie Collot, Viviane Baral, Sandrine Marlin, Tania Attie-Bitach, Irina Giurgea, Laurent Skopinski, William Reardon,[...]. Am J Hum Genet 2007
171
29

SOX10 mutations in patients with Waardenburg-Hirschsprung disease.
V Pingault, N Bondurand, K Kuhlbrodt, D E Goerich, M O Préhu, A Puliti, B Herbarth, I Hermans-Borgmeyer, E Legius, G Matthijs,[...]. Nat Genet 1998
625
26

Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences.
E Steingrímsson, K J Moore, M L Lamoreux, A R Ferré-D'Amaré, S K Burley, D C Zimring, L C Skow, C A Hodgkinson, H Arnheiter, N G Copeland. Nat Genet 1994
422
24

Melanocytes and the microphthalmia transcription factor network.
Eiríkur Steingrímsson, Neal G Copeland, Nancy A Jenkins. Annu Rev Genet 2004
528
23

Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome).
P Edery, T Attié, J Amiel, A Pelet, C Eng, R M Hofstra, H Martelli, C Bidaud, A Munnich, S Lyonnet. Nat Genet 1996
340
20

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene.
M Tassabehji, A P Read, V E Newton, R Harris, R Balling, P Gruss, T Strachan. Nature 1992
592
19


Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF.
S D Smith, P M Kelley, J B Kenyon, D Hoover. J Med Genet 2000
97
18

Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome.
N Bondurand, V Pingault, D E Goerich, N Lemort, E Sock, C Le Caignec, M Wegner, M Goossens. Hum Mol Genet 2000
333
17

microphthalmia, a critical factor in melanocyte development, defines a discrete transcription factor family.
T J Hemesath, E Steingrímsson, G McGill, M J Hansen, J Vaught, C A Hodgkinson, H Arnheiter, N G Copeland, N A Jenkins, D E Fisher. Genes Dev 1994
520
17

Restricted leucine zipper dimerization and specificity of DNA recognition of the melanocyte master regulator MITF.
Vivian Pogenberg, Margrét H Ogmundsdóttir, Kristín Bergsteinsdóttir, Alexander Schepsky, Bengt Phung, Viktor Deineko, Morlin Milewski, Eiríkur Steingrímsson, Matthias Wilmanns. Genes Dev 2012
73
20

Integrative genomic analyses identify MITF as a lineage survival oncogene amplified in malignant melanoma.
Levi A Garraway, Hans R Widlund, Mark A Rubin, Gad Getz, Aaron J Berger, Sridhar Ramaswamy, Rameen Beroukhim, Danny A Milner, Scott R Granter, Jinyan Du,[...]. Nature 2005
15

Hearing loss in Waardenburg syndrome: a systematic review.
J Song, Y Feng, F R Acke, P Coucke, K Vleminckx, I J Dhooge. Clin Genet 2016
57
26

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.
Corine Bertolotto, Fabienne Lesueur, Sandy Giuliano, Thomas Strub, Mahaut de Lichy, Karine Bille, Philippe Dessen, Benoit d'Hayer, Hamida Mohamdi, Audrey Remenieras,[...]. Nature 2011
336
14

Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium.
L A Farrer, K M Grundfast, J Amos, K S Arnos, J H Asher, P Beighton, S R Diehl, J Fex, C Foy, T B Friedman. Am J Hum Genet 1992
150
14


A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma.
Satoru Yokoyama, Susan L Woods, Glen M Boyle, Lauren G Aoude, Stuart MacGregor, Victoria Zismann, Michael Gartside, Anne E Cust, Rizwan Haq, Mark Harland,[...]. Nature 2011
285
13


Genetic and phenotypic heterogeneity in Chinese patients with Waardenburg syndrome type II.
Shuzhi Yang, Pu Dai, Xin Liu, Dongyang Kang, Xin Zhang, Weiyan Yang, Chengyong Zhou, Shiming Yang, Huijun Yuan. PLoS One 2013
27
48

Novel mutations of PAX3, MITF, and SOX10 genes in Chinese patients with type I or type II Waardenburg syndrome.
Hongsheng Chen, Lu Jiang, Zhiguo Xie, Lingyun Mei, Chufeng He, Zhengmao Hu, Kun Xia, Yong Feng. Biochem Biophys Res Commun 2010
55
23


The mutational spectrum in Waardenburg syndrome.
M Tassabehji, V E Newton, X Z Liu, A Brady, D Donnai, M Krajewska-Walasek, V Murday, A Norman, E Obersztyn, W Reardon. Hum Mol Genet 1995
168
12

Transcription factor hierarchy in Waardenburg syndrome: regulation of MITF expression by SOX10 and PAX3.
S B Potterf, M Furumura, K J Dunn, H Arnheiter, W J Pavan. Hum Genet 2000
263
12

Ser298 of MITF, a mutation site in Waardenburg syndrome type 2, is a phosphorylation site with functional significance.
K Takeda, C Takemoto, I Kobayashi, A Watanabe, Y Nobukuni, D E Fisher, M Tachibana. Hum Mol Genet 2000
134
12

Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease.
T Attié, M Till, A Pelet, J Amiel, P Edery, L Boutrand, A Munnich, S Lyonnet. Hum Mol Genet 1995
185
12

Oncogenic BRAF regulates oxidative metabolism via PGC1α and MITF.
Rizwan Haq, Jonathan Shoag, Pedro Andreu-Perez, Satoru Yokoyama, Hannah Edelman, Glenn C Rowe, Dennie T Frederick, Aeron D Hurley, Abhinav Nellore, Andrew L Kung,[...]. Cancer Cell 2013
551
11

MITF: master regulator of melanocyte development and melanoma oncogene.
Carmit Levy, Mehdi Khaled, David E Fisher. Trends Mol Med 2006
726
11

Biallelic Mutations in MITF Cause Coloboma, Osteopetrosis, Microphthalmia, Macrocephaly, Albinism, and Deafness.
Aman George, Dina J Zand, Robert B Hufnagel, Ruchi Sharma, Yuri V Sergeev, Janet M Legare, Gregory M Rice, Jessica A Scott Schwoerer, Mariana Rius, Laura Tetri,[...]. Am J Hum Genet 2016
46
23


MITF mutations associated with pigment deficiency syndromes and melanoma have different effects on protein function.
Christine Grill, Kristín Bergsteinsdóttir, Margrét H Ogmundsdóttir, Vivian Pogenberg, Alexander Schepsky, Matthias Wilmanns, Veronique Pingault, Eiríkur Steingrímsson. Hum Mol Genet 2013
36
27

A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome).
R M Hofstra, J Osinga, G Tan-Sindhunata, Y Wu, E J Kamsteeg, R P Stulp, C van Ravenswaaij-Arts, D Majoor-Krakauer, M Angrist, A Chakravarti,[...]. Nat Genet 1996
250
10

Mitf regulation of Dia1 controls melanoma proliferation and invasiveness.
Suzanne Carreira, Jane Goodall, Laurence Denat, Mercedes Rodriguez, Paolo Nuciforo, Keith S Hoek, Alessandro Testori, Lionel Larue, Colin R Goding. Genes Dev 2006
403
9

nacre encodes a zebrafish microphthalmia-related protein that regulates neural-crest-derived pigment cell fate.
J A Lister, C P Robertson, T Lepage, S L Johnson, D W Raible. Development 1999
537
9


Bcl2 regulation by the melanocyte master regulator Mitf modulates lineage survival and melanoma cell viability.
Gaël G McGill, Martin Horstmann, Hans R Widlund, Jinyan Du, Gabriela Motyckova, Emi K Nishimura, Yi-Ling Lin, Sridhar Ramaswamy, William Avery, Han-Fei Ding,[...]. Cell 2002
538
9

Epistatic relationship between Waardenburg syndrome genes MITF and PAX3.
A Watanabe, K Takeda, B Ploplis, M Tachibana. Nat Genet 1998
214
9

The recessive phenotype displayed by a dominant negative microphthalmia-associated transcription factor mutant is a result of impaired nucleation potential.
K Takebayashi, K Chida, I Tsukamoto, E Morii, H Munakata, H Arnheiter, T Kuroki, Y Kitamura, S Nomura. Mol Cell Biol 1996
98
9

c-Kit triggers dual phosphorylations, which couple activation and degradation of the essential melanocyte factor Mi.
M Wu, T J Hemesath, C M Takemoto, M A Horstmann, A G Wells, E R Price, D Z Fisher, D E Fisher. Genes Dev 2000
406
9

Essential role of microphthalmia transcription factor for DNA replication, mitosis and genomic stability in melanoma.
T Strub, S Giuliano, T Ye, C Bonet, C Keime, D Kobi, S Le Gras, M Cormont, R Ballotti, C Bertolotto,[...]. Oncogene 2011
166
9

Spectrum of novel mutations found in Waardenburg syndrome types 1 and 2: implications for molecular genetic diagnostics.
Gabriele Wildhardt, Birgit Zirn, Luitgard M Graul-Neumann, Juliane Wechtenbruch, Markus Suckfüll, Annegret Buske, Axel Bohring, Christian Kubisch, Stefanie Vogt, Gertrud Strobl-Wildemann,[...]. BMJ Open 2013
36
25

Screening program for Waardenburg syndrome in Colombia: clinical definition and phenotypic variability.
Marta L Tamayo, Nancy Gelvez, Marcela Rodriguez, Silvia Florez, Clara Varon, David Medina, Jaime E Bernal. Am J Med Genet A 2008
31
29

A de novo silencer causes elimination of MITF-M expression and profound hearing loss in pigs.
Lei Chen, Weiwei Guo, Lili Ren, Mingyao Yang, Yaofeng Zhao, Zongyi Guo, Haijin Yi, Mingzhou Li, Yiqing Hu, Xi Long,[...]. BMC Biol 2016
41
21


A helix-loop-helix transcription factor-like gene is located at the mi locus.
M J Hughes, J B Lingrel, J M Krakowsky, K P Anderson. J Biol Chem 1993
219
8

Identification of a novel isoform of microphthalmia-associated transcription factor that is enriched in retinal pigment epithelium.
S Amae, N Fuse, K Yasumoto, S Sato, I Yajima, H Yamamoto, T Udono, Y K Durlu, M Tamai, K Takahashi,[...]. Biochem Biophys Res Commun 1998
118
8

Mitf cooperates with Rb1 and activates p21Cip1 expression to regulate cell cycle progression.
Suzanne Carreira, Jane Goodall, Isil Aksan, S Anna La Rocca, Marie-Dominique Galibert, Laurence Denat, Lionel Larue, Colin R Goding. Nature 2005
283
8


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.