Katrien Stouffs

Also affiliated with Vrije Universiteit Brussel

Biochemistry, Genetics and Molecular BiologyMedicine

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 3 papers. Top paper: “Rare pathogenic variants in WNK3 cause X-linked intellectual disability”.

Rare pathogenic variants in WNK3 cause X-linked intellectual disability

Genetics in Medicine(2022)10.1016/j.gim.2022.05.009

N/A

0.416DataRank · unranked

15 citations

Jinwei Zhang, Thomas Besnard, Alfonso Caro‐Llopis, Xue Zeng, Stephanie M. Robert +75 more

Loss, Gain and Altered Function of GlyR α2 Subunit Mutations in Neurodevelopmental Disorders

Frontiers in Molecular Neuroscience(2022)10.3389/fnmol.2022.886729

N/A

0DataRank · unranked

18 citations

Katie A. Wilson, Natascha Schaefer, Lachlan De Hayr, Mark Windsor, Emmanuel Scalais +7 more

Overlapping cortical malformations in patients with pathogenic variants in GRIN1 and GRIN2B

Journal of Medical Genetics(2022)10.1136/jmedgenet-2021-107971

N/A

0DataRank · unranked

13 citations

Annie Laquerrière, Florent Marguet, Scott J. Myers, Yuan Hongjie, Diana Baralle +24 more