Pilar Alvarez Jerez
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Explore the profile of Pilar Alvarez Jerez including associated specialties, affiliations and a list of published articles.
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22
Citations
133
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Recent Articles
11.
Genner R, Akeson S, Meredith M, Jerez P, Malik L, Baker B, et al.
bioRxiv
. 2024 Mar;
PMID: 38464144
DNA methylation most commonly occurs as 5-methylcytosine (5-mC) in the human genome and has been associated with human diseases. Recent developments in single-molecule sequencing technologies (Oxford Nanopore Technologies (ONT) and...
12.
Busquets O, Li H, Syed K, Jerez P, Dunnack J, Lo Bu R, et al.
bioRxiv
. 2024 Feb;
PMID: 38405931
Parkinson's disease (PD) is a neurodegenerative disorder caused by complex genetic and environmental factors. Genome-edited human pluripotent stem cells (hPSCs) offer the uniique potential to advance our understanding of PD...
13.
Chen Z, Gustavsson E, Macpherson H, Anderson C, Clarkson C, Rocca C, et al.
Mov Disord
. 2024 Jan;
39(3):486-497.
PMID: 38197134
Background: Spinocerebellar ataxia type 4 (SCA4) is an autosomal dominant ataxia with invariable sensory neuropathy originally described in a family with Swedish ancestry residing in Utah more than 25 years...
14.
Kolmogorov M, Billingsley K, Mastoras M, Meredith M, Monlong J, Lorig-Roach R, et al.
Nat Methods
. 2023 Sep;
20(10):1483-1492.
PMID: 37710018
Long-read sequencing technologies substantially overcome the limitations of short-reads but have not been considered as a feasible replacement for population-scale projects, being a combination of too expensive, not scalable enough...
15.
Rizig M, Bandres-Ciga S, Makarious M, Ojo O, Wild Crea P, Abiodun O, et al.
Lancet Neurol
. 2023 Aug;
22(11):1015-1025.
PMID: 37633302
Background: An understanding of the genetic mechanisms underlying diseases in ancestrally diverse populations is an important step towards development of targeted treatments. Research in African and African admixed populations can...
16.
Rizig M, Bandres-Ciga S, Makarious M, Ojo O, Wild Crea P, Abiodun O, et al.
medRxiv
. 2023 Jul;
PMID: 37398408
Background: Understanding the genetic mechanisms underlying diseases in ancestrally diverse populations is a critical step towards the realization of the global application of precision medicine. The African and African admixed...
17.
Kaivola K, Chia R, Ding J, Rasheed M, Fujita M, Menon V, et al.
Cell Genom
. 2023 Jun;
3(6):100316.
PMID: 37388914
We characterized the role of structural variants, a largely unexplored type of genetic variation, in two non-Alzheimer's dementias, namely Lewy body dementia (LBD) and frontotemporal dementia (FTD)/amyotrophic lateral sclerosis (ALS)....
18.
Makarious M, Lake J, Pitz V, Fu A, Guidubaldi J, Warly Solsberg C, et al.
Brain
. 2023 Jun;
146(11):4622-4632.
PMID: 37348876
Parkinson's disease has a large heritable component and genome-wide association studies have identified over 90 variants with disease-associated common variants, providing deeper insights into the disease biology. However, there have...
19.
Leonard H, Murtadha R, Martinez-Carrasco A, Jama A, Muller-Nedebock A, Gil-Martinez A, et al.
NPJ Parkinsons Dis
. 2023 May;
9(1):77.
PMID: 37225742
No abstract available.
20.
Jerez P, Alcantud J, de Los Reyes-Ramirez L, Moore A, Ruz C, Vives Montero F, et al.
NPJ Parkinsons Dis
. 2023 Apr;
9(1):54.
PMID: 37024536
Neurodegeneration with brain iron accumulation (NBIA) represents a group of neurodegenerative disorders characterized by abnormal iron accumulation in the brain. In Parkinson's Disease (PD), iron accumulation is a cardinal feature...