Heidi Wallis

Associação de Assistência à Criança Deficiente

Biochemistry, Genetics and Molecular Biology

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: “ClinGen variant curation expert panel recommendations for classification of variants in GAMT, GATM and SLC6A8 for cerebral creatine deficiency syndromes”.

ClinGen variant curation expert panel recommendations for classification of variants in GAMT, GATM and SLC6A8 for cerebral creatine deficiency syndromes

Molecular Genetics and Metabolism(2024)10.1016/j.ymgme.2024.108362

N/A

0DataRank · unranked

10 citations

Amanda Thomas‐Wilson, Emily Groopman, Vimla S. Aggarwal, Simona Bianconi, Raquel Fernandez +9 more

Establishing a core outcome set for creatine transporter deficiency and guanidinoacetate methyltransferase deficiency

Orphanet Journal of Rare Diseases(2025)10.1186/s13023-025-03900-3

N/A

0DataRank · unranked

1 citations

Emily Reinhardt, Audrey Thurm, Beth K. Potter, Maureen Smith, Celeste Graham +25 more

Systematic Review of Patient Focused Drug Development Meeting Reports for Conditions Affecting Neurodevelopment

OSF Preprints (OSF Preprints)(2025)10.31234/osf.io/kx3dt_v1

N/A

0DataRank · unranked

0 citations

Victoria Kim, Tanvi Das, Seth Cutler, Heidi Wallis, Audrey Thurm +1 more