Elisabeth Tournier‐Lasserve

Also affiliated with Université Paris Cité, Sorbonne Université, Sorbonne Paris Cité, Institut du Cerveau

Medicine

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 11 papers. Top paper: “Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate”.

Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate

Brain(2021)10.1093/brain/awab432

N/A

0.696DataRank · unranked

35 citations

Cécile Duplàa, Dina Vojinović, Hideaki Suzuki, Nuno R. Zilhäo, Shuo Li +61 more

COL4A1/COL4A2 and inherited platelet disorder gene variants in fetuses showing intracranial hemorrhage

Prenatal Diagnosis(2022)10.1002/pd.6113

N/A

0DataRank · unranked

23 citations

Catherine Vincent‐Delorme, Morgane Stichelbout, Louise Devisme, A. Gélot, I. P. Deryabin +8 more

Lysyl hydroxylase 3–mediated post-translational modifications are required for proper biosynthesis of collagen α1α1α2(IV)

Journal of Biological Chemistry(2022)10.1016/j.jbc.2022.102713

N/A

0DataRank · unranked

19 citations

Yuki Taga, Thibault Coste, Sara F. Tufa, Douglas R. Keene, Kazunori Mizuno +3 more

Rare metabolic disease mimicking COL4A1 / COL4A2 fetal brain phenotype

Ultrasound in Obstetrics and Gynecology(2022)10.1002/uog.26046

N/A

0DataRank · unranked

4 citations

Chaker Aloui, F. Petit, S. Moutton, Louise Devisme, Celia Wells +6 more

Age-related loss of Notch3 underlies brain vascular contractility deficiencies, glymphatic dysfunction, and neurodegeneration in mice

Journal of Clinical Investigation(2023)10.1172/jci166134

N/A

0DataRank · unranked

54 citations

Russell H. Knutsen, Feiyang Ma, Ana Mompeón, Gloria E. Hernandez, Jocelynda Salvador +20 more

Rare variants in ANO1 , encoding a calcium-activated chloride channel, predispose to moyamoya disease

Brain(2023)10.1093/brain/awad172

N/A

0DataRank · unranked

26 citations

Wenlei Ye, Stuart Fraser, Jill A. Rosenfeld, Pavel N. Pichurin, Scott E. Hickey +19 more

Bi-allelic variants in the ESAM tight-junction gene cause a neurodevelopmental disorder associated with fetal intracranial hemorrhage

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.03.005

N/A

0DataRank · unranked

17 citations

Davut Pehli̇van, Damián Heine‐Suñer, Karin Weiss, Thibault Coste, Markus Zweier +42 more

Pathogenic SCN2A variants are associated with familial and sporadic hemiplegic migraine

Research Square(2023)10.21203/rs.3.rs-3215189/v1

N/A

0DataRank · unranked

4 citations

Christopher H. Thompson, Jean‐Marc DeKeyser, Tatiana Abramova, Steven Gazal, Thierry Moulin +7 more

PSAP‐Genomic‐Regions: A Method Leveraging Population Data to Prioritize Coding and Non‐Coding Variants in Whole Genome Sequencing for Rare Disease Diagnosis

Genetic Epidemiology(2024)10.1002/gepi.22593

N/A

0DataRank · unranked

2 citations

Ozvan Bocher, Chaker Aloui, Anne‐Louise Leutenegger, Ozan Özışık, Anaı̈s Baudot +7 more

Benchmark of computational methods to detect digenism in sequencing data

European Journal of Human Genetics(2025)10.1038/s41431-025-01834-9

N/A

0DataRank · unranked

2 citations

Donald F. Conrad, Anaı̈s Baudot, Elisabeth Tournier‐Lasserve, Principal investigators, Emmanuelle Génin +30 more

Exome Sequencing of Fetuses With Intracranial Hemorrhage Unravels Novel Causative Genes and an Extreme Genetic Heterogeneity

Prenatal Diagnosis(2025)10.1002/pd.6743

N/A

0DataRank · unranked

2 citations

Chaker Aloui, Justine Chanclud, Éléonore Blondiaux, Jéléna Martinovic, Tania Attié‐Bitach +10 more