Amelie J. Müller

Also affiliated with University of Tübingen

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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: “Disruption of MeCP2–TCF20 complex underlies distinct neurodevelopmental disorders”.

Disruption of MeCP2–TCF20 complex underlies distinct neurodevelopmental disorders

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2119078119

N/A

0.568DataRank · unranked

43 citations

Hamdan Hamdan, Hari Krishna Yalamanchili, Kaifang Pang, Amy E. Pohodich, Joanna Lopez +19 more

Rare predicted deleterious FEZF2 variants are associated with a neurodevelopmental phenotype

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63578

N/A

0.165DataRank · unranked

2 citations

Lisa Weingarten, Nicolas J. Abreu, Houda Zghal Elloumi, Tobias B. Haack, Clara Hildebrant +7 more

Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.06.015

N/A

0DataRank · unranked

55 citations

Mona Grimmel, Matias Wagner, J. Christopher Hennings, Christian Marx, René G. Feichtinger +41 more