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1

Homozygous CADPS2 Mutations Cause Neurodegenerative Disease..:

Lorenzo‐Betancor, Oswaldo ; Galosi, Livio ; Bonfili, Laura...
Movement Disorders.  37 (2022)  12 - p. 2345-2354 , 2022
Link: https://doi.org/10.1002/..
 
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2

PNPLA6‐Related Disorder with Levodopa‐Responsive Parkinsoni..:

Kazanci, Serdar ; Witt, Jennifer ; Su, Kimmy...
Movement Disorders Clinical Practice.  10 (2022)  2 - p. 338-340 , 2022
Link: https://doi.org/10.1002/..
 
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3

Homozygous CADPS2 mutations cause neurodegenerative disease..:

Lorenzo-Betancor, Oswaldo ; Galosi, Livio ; Bonfili, Laura...
Neurology.  98 (2022)  18_supplement - p. , 2022
Link: https://doi.org/10.1212/..
 
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4

Novel compound heterozygous FBXO7 mutations in a family wit..:

Lorenzo-Betancor, Oswaldo ; Lin, Yi-Han ; Samii, Ali...
Parkinsonism & Related Disorders.  80 (2020)  - p. 142-147 , 2020
Link: https://doi.org/10.1016/..
 
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5

The distribution and risk effect of GBA variants in a large..:

Velez-Pardo, Carlos ; Lorenzo-Betancor, Oswaldo ; Jimenez-Del-Rio, Marlene...
Parkinsonism & Related Disorders.  63 (2019)  - p. 204-208 , 2019
Link: https://doi.org/10.1016/..
 
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6

Erratum: Variable frequency of LRRK2 variants in the Latin ..:

Cornejo-Olivas, Mario ; Torres, Luis ; Velit-Salazar, Mario R....
npj Parkinson's Disease.  4 (2018)  1 - p. , 2018
Link: https://doi.org/10.1038/..
 
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7

Variable frequency of LRRK2 variants in the Latin American ..:

Cornejo-Olivas, Mario ; Torres, Luis ; Velit-Salazar, Mario R....
npj Parkinson's Disease.  3 (2017)  1 - p. , 2017
Link: https://doi.org/10.1038/..
 
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8

Large-scale exploratory genetic analysis of cognitive impai..:

Mata, Ignacio F. ; Johnson, Catherine O. ; Leverenz, James B....
Neurobiology of Aging.  56 (2017)  - p. 211.e1-211.e7 , 2017
Link: https://doi.org/10.1016/..
 
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9

Smoking and haptoglobin phenotype modulate serum ferritin a..:

Costa-Mallen, Paola ; Zabetian, Cyrus P. ; Hu, Shu-Ching...
Journal of Neural Transmission.  123 (2016)  11 - p. 1319-1330 , 2016
Link: https://doi.org/10.1007/..
 
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10

The discovery of LRRK2 p.R1441S, a novel mutation for Parki..:

Mata, Ignacio F. ; Davis, Marie Y. ; Lopez, Alexis N....
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.  171 (2016)  7 - p. 925-930 , 2016
Link: https://doi.org/10.1002/..
 
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11

Response to the letter "Haptoglobin phenotype and Parkinson..:

Costa-Mallen, Paola ; Zabetian, Cyrus P. ; Agarwal, Pinky...
Parkinsonism & Related Disorders.  22 (2016)  - p. 110-111 , 2016
Link: https://doi.org/10.1016/..
 
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12

The discovery of LRRK2 p.R1441S, a novel mutation for Parki..:

Mata, Ignacio F. ; Davis, Marie Y. ; Lopez, Alexis N....
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.  174 (2016)  1 - p. 113-113 , 2016
Link: https://doi.org/10.1002/..
 
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13

GBA Variants are associated with a distinct pattern of cogn..:

Mata, Ignacio F. ; Leverenz, James B. ; Weintraub, Daniel...
Movement Disorders.  31 (2015)  1 - p. 95-102 , 2015
Link: https://doi.org/10.1002/..
 
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14

Haptoglobin phenotype modifies serum iron levels and the ef..:

Costa-Mallen, Paola ; Zabetian, Cyrus P. ; Agarwal, Pinky...
Parkinsonism & Related Disorders.  21 (2015)  9 - p. 1087-1092 , 2015
Link: https://doi.org/10.1016/..
 
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15

The RAB39B p.G192R mutation causes X-linked dominant Parkin..:

Mata, Ignacio F. ; Jang, Yongwoo ; Kim, Chun-Hyung...
Molecular Neurodegeneration.  10 (2015)  1 - p. , 2015
Link: https://doi.org/10.1186/..
 
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