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🐜
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Sequencing of diverse mandarin, pummelo and orange genomes reveals complex history of admixture during citrus domestication
55 auth.
G. A. Wu,
S. Prochnik,
J. Jenkins,
J. Salse,
U. Hellsten,
Florent Murat,
X. Perrier,
M. Ruiz,
S. Scalabrin,
J. Terol,
M. Takita,
K. Labadie,
J. Poulain,
A. Couloux,
K. Jabbari,
...
F. Cattonaro,
Cristian Del Fabbro,
S. Pinosio,
A. Zuccolo,
Jarrod Chapman,
J. Grimwood,
F. Tadeo,
L. H. Estornell,
J. V. Muñoz-Sanz,
Victoria Ibanez,
Amparo Herrero-Ortega,
P. Aleza,
Julián Pérez-Pérez,
D. Ramón,
D. Brunel,
F. Luro,
Chunxian Chen,
W. Farmerie,
B. Desany,
C. Kodira,
M. Mohiuddin,
T. Harkins,
Karin M. Fredrikson,
P. Burns,
A. Lomsadze,
M. Borodovsky,
Giuseppe Reforgiato,
J. Freitas-Astúa,
F. Quétier,
L. Navarro,
M. Roose,
P. Wincker,
J. Schmutz,
M. Morgante,
M. A. Machado,
M. Talón,
O. Jaillon,
P. Ollitrault,
F. Gmitter,
D. Rokhsar
|
8 |
2014 |
8
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|
|
🐢
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C9ORF72 hexanucleotide expansions of 20–22 repeats are associated with frontotemporal deterioration
11 auth.
E. Gómez-Tortosa,
J. Gallego,
R. Guerrero‐López,
A. Marcos,
E. Gil-Neciga,
M. J. Sainz,
...
A. Díaz,
E. Franco-Macías,
M. Trujillo-Tiebas,
C. Ayuso,
Julián Pérez-Pérez
|
6 |
2013 |
6
🐢
|
|
🐜
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Clinical-genetic correlations in familial Alzheimer's disease caused by presenilin 1 mutations.
15 auth.
E. Gómez-Tortosa,
S. Barquero,
M. Barón,
E. Gil-Neciga,
F. Castellanos,
M. Zurdo,
S. Manzano,
David G. Muñoz,
A. Jiménez‐Huete,
A. Rábano,
...
M. J. Sainz,
R. Guerrero,
I. Gobernado,
Julián Pérez-Pérez,
A. Jiménez-Escrig
|
5 |
2010 |
5
🐜
|
|
🐜
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Relevance of complement factor H-related 1 (CFHR1) genotypes in age-related macular degeneration.
9 auth.
Ruben Martinez-Barricarte,
S. Recalde,
P. Fernández-Robredo,
I. Millán,
L. Olavarrieta,
Antonio Viñuela,
...
Julián Pérez-Pérez,
A. García-Layana,
S. Rodríguez de Córdoba
|
5 |
2012 |
5
🐜
|
|
🐜
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Association between CFH, CFB, ARMS2, SERPINF1, VEGFR1 and VEGF polymorphisms and anatomical and functional response to ranibizumab treatment in neovascular age‐related macular degeneration
14 auth.
E. Cobos,
S. Recalde,
J. Anter,
M. Hernández-Sánchez,
Carla Barreales,
L. Olavarrieta,
Alicia Valverde,
M. Suarez-Figueroa,
F. Cruz,
M. Abraldes,
...
Julián Pérez-Pérez,
P. Fernández-Robredo,
L. Arias,
A. García-Layana
|
5 |
2018 |
5
🐜
|
|
🐜
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Mutation affecting the proximal promoter of Endoglin as the origin of hereditary hemorrhagic telangiectasia type 1
8 auth.
Virginia Albiñana,
Mª. Paz Zafra,
J. Colau,
R. Zarrabeitia,
Lucía Recio-Poveda,
L. Olavarrieta,
...
Julián Pérez-Pérez,
L. Botella
|
4 |
2017 |
4
🐜
|
|
🐜
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Familial primary lateral sclerosis or dementia associated with Arg573Gly TBK1 mutation
13 auth.
E. Gómez-Tortosa,
J. van der Zee,
M. Ruggiero,
I. Gijselinck,
J. Esteban-Pérez,
A. García-Redondo,
D. Borrego-Hernández,
E. Navarro,
José M. Sainz,
Julián Pérez-Pérez,
...
M. Cruts,
C. van Broeckhoven,
R. Guerrero‐López
|
4 |
2017 |
4
🐜
|
|
🐬
|
Familial benign frontotemporal deterioration with C9ORF72 hexanucleotide expansion
E. Gómez-Tortosa,
Soledad Serrano,
M. D. Toledo,
Julián Pérez-Pérez,
M. J. Sainz
|
4 |
2014 |
4
🐬
|
|
🐜
|
α-Secretase nonsense mutation (ADAM10 Tyr167*) in familial Alzheimer’s disease
9 auth.
Pablo Agüero,
M. J. Sainz,
M. García‐Ayllón,
J. Sáez-Valero,
R. Téllez,
R. Guerrero‐López,
...
Julián Pérez-Pérez,
A. Jiménez-Escrig,
E. Gómez-Tortosa
|
4 |
2020 |
4
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