Francis Rossignol

National Human Genome Research Institute

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 9 papers. Top paper: “Patient-reported outcomes and functional assessments of patients with Alkaptonuria in a 3-year Nitisinone treatment trial”.

Patient-reported outcomes and functional assessments of patients with Alkaptonuria in a 3-year Nitisinone treatment trial

Molecular Genetics and Metabolism(2024)10.1016/j.ymgme.2024.108562

N/A

0.269DataRank · unranked

5 citations

Francis Rossignol, Monique B. Perry, Michael A. Kayser, Pim Suwannarat, Kevin E. O'Brien +6 more

Deep Learning Study of Alkaptonuria Spinal Disease Assesses Global and Regional Severity and Detects Occult Treatment Status

Journal of Inherited Metabolic Disease(2025)10.1002/jimd.70042

N/A

0.165DataRank · unranked

2 citations

Vibha Chandrasekar, Irene J. Castillo, Dat Duong, Carlos R. Ferreira, Suzanna Ledgister Hanchard +6 more

Phase 1 Study of Oral N-Acetylmannosamine in Primary Podocytopathies

Kidney International Reports(2025)10.1016/j.ekir.2025.103758

N/A

0.104DataRank · unranked

1 citations

Anirban Ganguli, Jonathan Bolaños, Petcharat Leoyklang, Kenneth J. Wilkins, Yi Arial Zeng +10 more

Clinical and biochemical footprints of inherited metabolic diseases: XVII. Dysmorphisms

Molecular Genetics and Metabolism(2024)10.1016/j.ymgme.2024.109001

N/A

0.104DataRank · unranked

1 citations

Sofia Saenz-Ayala, Erin T. Strovel, Francis Rossignol, Carlos R. Ferreira, Nenad Blau +1 more

Quantitative analysis of the natural history of prolidase deficiency: description of 17 families and systematic review of published cases

Genetics in Medicine(2021)10.1038/s41436-021-01200-2

N/A

0DataRank · unranked

26 citations

Marvid S. Duarte Moreno, Jean‐François Benoist, Manfred Boehm, E. Bourrat, Aline Cano +28 more

Development of a radiographic vertebral severity score for evaluation of disease progression in alkaptonuria

Molecular Genetics and Metabolism(2025)10.1016/j.ymgme.2025.109251

N/A

0DataRank · unranked

0 citations

Kristen S. Pan, Monique B. Perry, Joy Bryant, Kevin O’Brien, Irene J. Castillo +7 more

ATP1A1-linked diseases require a malfunctioning protein product from one allele

Biochimica et Biophysica Acta (BBA) - Molecular Cell Research(2023)10.1016/j.bbamcr.2023.119572

N/A

0DataRank · unranked

4 citations

Victoria C. Young, Ryan Sweazey, Alexandria Padro, Jeannie K. Lee, Tulio Bueso +12 more

ATP1A1 -linked diseases require a malfunctioning protein product from one allele

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.03.05.531165

N/A

0DataRank · unranked

0 citations

Victoria C. Young, Ryan Sweazey, Alexandria Padro, Jeannie K. Lee, Tulio Bueso +12 more

Glycerophospholipids: Roles in Cell Trafficking and Associated Inborn Errors

Journal of Inherited Metabolic Disease(2025)10.1002/jimd.70019

N/A

0DataRank · unranked

39 citations

Francis Rossignol, Grant A. Mitchell, Foudil Lamari