Search details
1.
IntroVerse: a comprehensive database of introns across human tissues.
Nucleic Acids Res
; 51(D1): D167-D178, 2023 01 06.
Article
in English
| MEDLINE | ID: mdl-36399497
2.
Artificial intelligence for dementia genetics and omics.
Alzheimers Dement
; 19(12): 5905-5921, 2023 Dec.
Article
in English
| MEDLINE | ID: mdl-37606627
3.
PhenoExam: gene set analyses through integration of different phenotype databases.
BMC Bioinformatics
; 23(1): 567, 2022 Dec 31.
Article
in English
| MEDLINE | ID: mdl-36587217
4.
Trem2 promotes anti-inflammatory responses in microglia and is suppressed under pro-inflammatory conditions.
Hum Mol Genet
; 29(19): 3224-3248, 2020 11 25.
Article
in English
| MEDLINE | ID: mdl-32959884
5.
Modeling multifunctionality of genes with secondary gene co-expression networks in human brain provides novel disease insights.
Bioinformatics
; 37(18): 2905-2911, 2021 09 29.
Article
in English
| MEDLINE | ID: mdl-33734320
6.
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsies.
Neuropathol Appl Neurobiol
; 48(1): e12758, 2022 02.
Article
in English
| MEDLINE | ID: mdl-34388852
7.
A genetic link between risk for Alzheimer's disease and severe COVID-19 outcomes via the OAS1 gene.
Brain
; 144(12): 3727-3741, 2021 12 31.
Article
in English
| MEDLINE | ID: mdl-34619763
8.
ASL expression in ALDH1A1+ neurons in the substantia nigra metabolically contributes to neurodegenerative phenotype.
Hum Genet
; 140(10): 1471-1485, 2021 Oct.
Article
in English
| MEDLINE | ID: mdl-34417872
9.
Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders.
Brain
; 143(9): 2771-2787, 2020 09 01.
Article
in English
| MEDLINE | ID: mdl-32889528
10.
Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination.
Am J Hum Genet
; 100(6): 969-977, 2017 Jun 01.
Article
in English
| MEDLINE | ID: mdl-28575651
11.
PDXK mutations cause polyneuropathy responsive to pyridoxal 5'-phosphate supplementation.
Ann Neurol
; 86(2): 225-240, 2019 08.
Article
in English
| MEDLINE | ID: mdl-31187503
12.
Transcriptomic and genetic analyses reveal potential causal drivers for intractable partial epilepsy.
Brain
; 142(6): 1616-1630, 2019 06 01.
Article
in English
| MEDLINE | ID: mdl-30932156
13.
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination.
Brain
; 142(10): 2948-2964, 2019 10 01.
Article
in English
| MEDLINE | ID: mdl-31501903
14.
Correction to: Picomolar concentrations of oligomeric alpha-synuclein sensitizes TLR4 to play an initiating role in Parkinson's disease pathogenesis.
Acta Neuropathol
; 137(1): 121, 2019 Jan.
Article
in English
| MEDLINE | ID: mdl-30328509
15.
Picomolar concentrations of oligomeric alpha-synuclein sensitizes TLR4 to play an initiating role in Parkinson's disease pathogenesis.
Acta Neuropathol
; 137(1): 103-120, 2019 01.
Article
in English
| MEDLINE | ID: mdl-30225556
16.
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study.
Brain
; 141(2): 391-408, 2018 02 01.
Article
in English
| MEDLINE | ID: mdl-29365066
17.
A loss-of-function homozygous mutation in DDX59 implicates a conserved DEAD-box RNA helicase in nervous system development and function.
Hum Mutat
; 39(2): 187-192, 2018 02.
Article
in English
| MEDLINE | ID: mdl-29127725
18.
Gene co-expression networks shed light into diseases of brain iron accumulation.
Neurobiol Dis
; 87: 59-68, 2016 Mar.
Article
in English
| MEDLINE | ID: mdl-26707700
19.
Circulating blood circular RNA in Parkinson's Disease; a systematic study.
medRxiv
; 2024 Jan 23.
Article
in English
| MEDLINE | ID: mdl-38343838
20.
Paired plasma lipidomics and proteomics analysis in the conversion from mild cognitive impairment to Alzheimer's disease.
Comput Biol Med
; 176: 108588, 2024 Jun.
Article
in English
| MEDLINE | ID: mdl-38761503