Mehrdad A. Estiar

Also affiliated with Montreal Neurological Institute and Hospital, Harvard University, McGill University, Massachusetts Institute of Technology

NeuroscienceMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 10 papers. Top paper: “Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects”.

Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects

Nature Communications(2022)10.1038/s41467-022-34732-5

N/A

1.7DataRank · unranked

95 citations

Karl Heilbron, Cornelis Blauwendraat, Regina Hertfelder Reynolds, Eric Yu, Konstantin Senkevich +95 more

Analysis of heterozygous PRKN variants and copy number variations in Parkinson’s disease

medRxiv(2020)10.1101/2020.05.07.20072728

N/A

0DataRank · unranked

2 citations

Uladzislau Rudakou, Lynne Krohn, Kheireddin Mufti, Jennifer A. Ruskey, Farnaz Asayesh +15 more

Fine mapping of the HLA locus in Parkinson’s disease in Europeans

medRxiv(2020)10.1101/2020.10.29.20217059

N/A

0DataRank · unranked

1 citations

Aditya Ambati, Maren Stolp Andersen, Lynne Krohn, Mehrdad A. Estiar, Prabhjyot Saini +14 more

Fine mapping of the HLA locus in Parkinson’s disease in Europeans

npj Parkinson s Disease(2021)10.1038/s41531-021-00231-5

N/A

0DataRank · unranked

74 citations

Aditya Ambati, Maren Stolp Andersen, Lynne Krohn, Mehrdad A. Estiar, Prabhjyot Saini +14 more

Lack of Causal Effects or Genetic Correlation between Restless Legs Syndrome and Parkinson's Disease

Movement Disorders(2021)10.1002/mds.28640

N/A

0DataRank · unranked

13 citations

Konstantin Senkevich, Eric Yu, Parizad Varghaei, Lynne Krohn, Sara Bandrés‐Ciga +4 more

Genome-wide association study of REM sleep behavior disorder identifies novel loci with distinct polygenic and brain expression effects

medRxiv(2021)10.1101/2021.09.08.21254232

N/A

0DataRank · unranked

8 citations

Karl Heilbron, Cornelis Blauwendraat, Regina Hertfelder Reynolds, Eric Yu, Konstantin Senkevich +53 more

BiP inactivation due to loss of the deAMPylation function of FICD causes a motor neuron disease

Genetics in Medicine(2022)10.1016/j.gim.2022.08.019

N/A

0DataRank · unranked

30 citations

Ariel Ruiz, Maike F. Dohrn, Melanie Wayand, Amjad Farooq, Matt C. Danzi +14 more

TCEAL1 loss-of-function results in an X-linked dominant neurodevelopmental syndrome and drives the neurological disease trait in Xq22.2 deletions

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.10.007

N/A

0DataRank · unranked

26 citations

Linda M. Reis, Davut Pehli̇van, Jonathan A. Bernstein, Michael Muriello, Erin Syverson +33 more

Analysis of Heterozygous PRKN Variants and Copy‐Number Variations in Parkinson's Disease

Movement Disorders(2020)10.1002/mds.28299

N/A

0DataRank · unranked

49 citations

Uladzislau Rudakou, Lynne Krohn, Kheireddin Mufti, Jennifer A. Ruskey, Farnaz Asayesh +15 more

From spastic paraplegia to infantile neurodegenerative disorder: Expanding the phenotypic spectrum associated with biallelic SPAST variants

European Journal of Neurology(2024)10.1111/ene.70025

N/A

0DataRank · unranked

6 citations

Chloé Angelini, Claire Bar, Wahiba Amer El Khedoud, Christine Barnérias, Razika Boulariah‐Hadjou +15 more