M. Sabir

发表

The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population‐Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight

Sonja W. Scholz, D. Hernandez, M. Nalls, 2019, Movement disorders : official journal of the Movement Disorder Society.

The genetic architecture of Parkinson disease in Spain: characterizing population-specific risk, differential haplotype structures, and providing etiologic insight

Sonja W. Scholz, D. Hernandez, M. Nalls, 2019, bioRxiv.

Pomegranate derivative urolithin A enhances vitamin D receptor signaling to amplify serotonin-related gene induction by 1,25-dihydroxyvitamin D

M. Haussler, P. Jurutka, M. Sabir, 2020, Biochemistry and biophysics reports.

Vitamin D Nutrient-Gene Interactions and Healthful Aging

Zainab N. Khan, M. Haussler, P. Jurutka, 2016 .

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

Timothy A. Miller, Jennifer E. Phillips-Cremins, Lilah M. Besser, 2020, Neuron.

Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia

Sonja W. Scholz, D. Hernandez, M. Nalls, 2019, bioRxiv.

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into the complex genetic architecture

Sonja W. Scholz, Lilah M. Besser, Alan J. Thomas, 2020, bioRxiv.

α‐Synuclein Deposition in Sympathetic Nerve Fibers in Genetic Forms of Parkinson's Disease

Sonja W. Scholz, C. Blauwendraat, D. Goldstein, 2021, Movement disorders : official journal of the Movement Disorder Society.

Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease

Sonja W. Scholz, Demis A. Kia, D. Hernandez, 2018, JAMA neurology.

MAPT p.V363I mutation

Sonja W. Scholz, J. Troncoso, P. Pástor, 2019, Neurology: Genetics.

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

Sonja W. Scholz, Hannah A. Pliner, Janel O. Johnson, 2021, JAMA neurology.

Mutations in the SPTLC1 gene are a cause of amyotrophic lateral sclerosis that may be amenable to serine supplementation

Sonja W. Scholz, Hannah A. Pliner, Janel O. Johnson, 2019, bioRxiv.

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.

Timothy A. Miller, Sonja W. Scholz, Jennifer E. Phillips-Cremins, 2020, Neuron.

MAPT p.V363I mutation A rare cause of corticobasal degeneration

Sonja W. Scholz, C. Morris, J. Troncoso, 2022 .

Bioactive Dietary VDR Ligands Regulate Genes Encoding Biomarkers of Skin Repair That Are Associated with Risk for Psoriasis

M. Haussler, P. Jurutka, M. Sabir, 2018, Nutrients.

Identification of putative transcriptomic biomarkers in irritable bowel syndrome (IBS): Differential gene expression and regulation of TPH1 and SERT by vitamin D

P. Jurutka, M. Sabir, L. Harris, 2022, PloS one.

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

Sonja W. Scholz, Lilah M. Besser, Alan J. Thomas, 2021, Nature Genetics.

LRP10 in α-synucleinopathies

Sonja W. Scholz, D. Hernandez, M. Nalls, 2018, The Lancet Neurology.

Implications of language barrier on the diagnostic yield of computed tomography in pulmonary embolism

M. Sabir, J. Stowell, M. Akhter, 2017, The American journal of emergency medicine.

1,25-Dihydroxyvitamin D and Klotho: A Tale of Two Renal Hormones Coming of Age.

Zainab N. Khan, M. Haussler, P. Jurutka, 2016, Vitamins and hormones.

Gene Expression Profiling and Assessment of Vitamin D and Serotonin Pathway Variations in Patients With Irritable Bowel Syndrome

C. Borror, P. Jurutka, S. Yale, 2018, Journal of neurogastroenterology and motility.

Optimal vitamin D spurs serotonin: 1,25-dihydroxyvitamin D represses serotonin reuptake transport (SERT) and degradation (MAO-A) gene expression in cultured rat serotonergic neuronal cell lines

M. Haussler, P. Jurutka, M. Sabir, 2018, Genes & nutrition.

Genetic analysis of neurodegenerative diseases in a pathology cohort

Sonja W. Scholz, M. Nalls, L. Ferrucci, 2019, Neurobiology of Aging.

A rare cause of corticobasal degeneration

Sonja W. Scholz, C. Morris, J. Troncoso, 2022 .

1,25‐Dihydroxyvitamin D regulates expression of the tryptophan hydroxylase 2 and leptin genes: implication for behavioral influences of vitamin D

P. Jurutka, J. Hsieh, M. Sabir, 2015, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.

Sonja W. Scholz, D. Hernandez, M. Nalls, 2019, Brain : a journal of neurology.

Assessment of APOE in atypical parkinsonism syndromes

Sonja W. Scholz, D. Hernandez, C. Blauwendraat, 2019, Neurobiology of Disease.

SIRT1 enzymatically potentiates 1,25-dihydroxyvitamin D3 signaling via vitamin D receptor deacetylation

Zainab N. Khan, E. Jacobs, M. Galligan, 2017, The Journal of Steroid Biochemistry and Molecular Biology.

Resveratrol Potentiates Vitamin D and Nuclear Receptor Signaling

E. Jacobs, M. Haussler, P. Jurutka, 2015, Journal of cellular biochemistry.