Publicacions
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Olival J, Hoenicka J, Arca-Diaz G, Arnaez-Solis J, Agut-Quijano T, Maynou-Fernández J, Stephan-Otto C, Nuñez C, Benavente I, Simon Pedro Lubian López, Palau F and García-Alix A.
Idiopathic neonatal arterial ischaemic stroke: a trio-based whole-exome sequencing study.
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION . : .
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Step K, Hernández CF, Khani M, Eltaraifee E, Hernández-Medrano AJ, Kung PJ, Ostrožovicová M, Zirra A, Pérez-Palma E, Mencacci NE, Keller Sarmiento IJ, Morris HR, Mata IF, Acosta-Uribe J, Fang ZH and Bandres-Ciga S.
Genome-Wide Assessment Reveals Ancestral Differences in Homozygosity Patterns Potentially Linked to Parkinson's Disease Etiology.
MOVEMENT DISORDERS . : .
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Landoulsi Z, Sreelatha AAK, Kuznetsov N, Schulte C, Bobbili DR, Montanucci L, Leu C, Niestroj LM, Hassanin E, Domenighetti C, Sugier PE, Radivojkov-Blagojevic M, Lichtner P, Portugal B, Edsall C, Krüger J, Hernandez DG, Blauwendraat C, Mellick GD, Zimprich A, Pirker W, Tan M, Rogaeva E, Lang A, Koks S, Taba P, Lesage S, Brice A, Corvol JC, Chartier-Harlin MC, Mutez E, Brockmann K, Deutschländer AB, Hadjigeorgiou GM, Dardiotis E, Stefanis L, Simitsi AM, Valente EM, Petrucci S, Straniero L, Zecchinelli A, Pezzoli G, Brighina L, Ferrarese C, Annesi G, Quattrone A, Gagliardi M, Burbulla LF, Matsuo H, Nakayama A, Hattori N, Nishioka K, Chung SJ, Kim YJ, Pavelka L, Kolber P, van de Warrenburg BP, Bloem BR, Singleton AB, Vitale D, Toft M, Pihlstrom L, Guedes LC, Ferreira JJ, Bardien S, Carr J, Tolosa E, Ezquerra M, Pastor P, Wirdefeldt K, Pedersen NL, Ran C, Belin AC, Puschmann A, Clarke CE, Morrison KE, Krainc D, Farrer MJ, Lal D, Elbaz A, Gasser T, Krüger R, Sharma M and May P.
Genome-wide association study of copy number variations in Parkinson's disease.
npj Parkinsons Disease . : .
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Chu YT, Su YA, Lin CH, Tai CH, Wu YR, Hong CT, Chen YW, Tsai MH, Hardy J, Mok KY and Wu RM.
Genome-wide association and population-tailored polygenic risk for Parkinson's disease in Taiwan.
npj Parkinsons Disease . : .
