Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

Iñaki Comino-Méndez; Francisco J Gracia-Aznárez; Francesca Schiavi; Iñigo Landa; Luis J Leandro-García; Rocío Letón; Emiliano Honrado; Rocío Ramos-Medina; Daniela Caronia; Guillermo Pita; Álvaro Gómez-Graña; Aguirre A de Cubas; Lucía Inglada-Pérez; Agnieszka Maliszewska; Elisa Taschin; Sara Bobisse; Giuseppe Pica; Paola Loli; Rafael Hernández-Lavado; José A Díaz; Mercedes Gómez-Morales; Anna González-Neira; Giovanna Roncador; Cristina Rodríguez-Antona; Javier Benítez; Massimo Mannelli; Giuseppe Opocher; Mercedes Robledo; Alberto Cascón

doi:10.1038/ng.861

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

Nature Genetics ◽

10.1038/ng.861 ◽

2011 ◽

Vol 43 (7) ◽

pp. 663-667 ◽

Cited By ~ 347

Author(s):

Iñaki Comino-Méndez ◽

Francisco J Gracia-Aznárez ◽

Francesca Schiavi ◽

Iñigo Landa ◽

Luis J Leandro-García ◽

...

Keyword(s):

Exome Sequencing ◽

Hereditary Pheochromocytoma

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Faculty Opinions recommendation of Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.11636959.14701058 ◽

2011 ◽

Author(s):

Barry Nelkin

Keyword(s):

Exome Sequencing ◽

Hereditary Pheochromocytoma

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Faculty Opinions recommendation of Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.11636959.12843054 ◽

2011 ◽

Author(s):

Patricia Dahia

Keyword(s):

Exome Sequencing ◽

Hereditary Pheochromocytoma

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Faculty Opinions recommendation of Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.11636959.14753066 ◽

2011 ◽

Author(s):

Peter Fuller

Keyword(s):

Exome Sequencing ◽

Hereditary Pheochromocytoma

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Faculty Opinions recommendation of Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.11636959.12697057 ◽

2011 ◽

Author(s):

Gilbert Cote

Keyword(s):

Exome Sequencing ◽

Hereditary Pheochromocytoma

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Faculty Opinions recommendation of Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.11636959.14542269 ◽

2011 ◽

Author(s):

Robert Dluhy ◽

Florencia Halperin

Keyword(s):

Exome Sequencing ◽

Hereditary Pheochromocytoma

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Exome sequencing takes centre stage in cancer profiling

Nature ◽

10.1038/459146b ◽

2009 ◽

Cited By ~ 24

Author(s):

Brendan Maher

Keyword(s):

Exome Sequencing

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Molecular diagnosis in mitochondrial respiratory chain deficiency using exome sequencing

Neuropediatrics ◽

10.1055/s-0033-1337715 ◽

2013 ◽

Vol 44 (02) ◽

Author(s):

R Kopajtich ◽

T Haack ◽

B Haberberger ◽

J Mayr ◽

W Sperl ◽

...

Keyword(s):

Exome Sequencing ◽

Respiratory Chain ◽

Molecular Diagnosis ◽

Mitochondrial Respiratory Chain ◽

Respiratory Chain Deficiency ◽

Mitochondrial Respiratory

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Whole Exome Sequencing (WES) in Familien mit linksventrikulärer Ausfluβtraktobstruktion (LVOTO)

The Thoracic and Cardiovascular Surgeon ◽

10.1055/s-0034-1393993 ◽

2014 ◽

Vol 62 (S 02) ◽

Author(s):

M. Hitz ◽

S. Al-Turki ◽

A. Schalinski ◽

U. Bauer ◽

T. Pickardt ◽

...

Keyword(s):

Exome Sequencing ◽

Whole Exome Sequencing ◽

Whole Exome

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Identification of Novel Germline and Tumor-Specific Nucleotide Variants and Copy Number Variation in Clival Chordomas by Exome Sequencing

Journal of Neurological Surgery Part B Skull Base ◽

10.1055/s-0035-1546555 ◽

2015 ◽

Vol 76 (S 01) ◽

Author(s):

Georgios Zenonos ◽

Peter Howard ◽

Maureen Lyons-Weiler ◽

Wang Eric ◽

William LaFambroise ◽

...

Keyword(s):

Copy Number Variation ◽

Exome Sequencing ◽

Copy Number ◽

Number Variation ◽

Specific Nucleotide

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Exome sequencing and case-control analyses identify RCC1 as a candidate breast cancer susceptibility gene

10.1055/s-0038-1671215 ◽

2018 ◽

Author(s):

A Riahi ◽

H Radmanesh ◽

P Schürmann ◽

N Bogdanova ◽

R Geffers ◽

...

Keyword(s):

Breast Cancer ◽

Exome Sequencing ◽

Cancer Susceptibility ◽

Susceptibility Gene ◽

Breast Cancer Susceptibility ◽

Case Control ◽

Breast Cancer Susceptibility Gene ◽

Cancer Susceptibility Gene

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