Christine Bellanné‐Chantelot

Also affiliated with Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital

MedicineBiochemistry, Genetics and Molecular BiologyImmunology and Microbiology

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

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 6 papers. Top paper: “Inherited GATA2 Deficiency Is Dominant by Haploinsufficiency and Displays Incomplete Clinical Penetrance”.

Inherited GATA2 Deficiency Is Dominant by Haploinsufficiency and Displays Incomplete Clinical Penetrance

Journal of Clinical Immunology(2021)10.1007/s10875-020-00930-3

N/A

1.4DataRank · unranked

49 citations

Edgar Borges de Oliveira-Júnior, Jérémie Rosain, Franck Rapaport, Caroline Deswarte, Antoine Guérin +55 more

Variants influencing age at diagnosis of HNF1A-MODY

Molecular Medicine(2022)10.1186/s10020-022-00542-0

N/A

0.360DataRank · unranked

10 citations

Michał T. Seweryn, Piotr Radkowski, Przemysław Kapusta, Julita Machlowska, Štěpánka Průhová +11 more

An inherited gain‐of‐function risk allele in EPOR predisposes to familial JAK2V617F myeloproliferative neoplasms

British Journal of Haematology(2022)10.1111/bjh.18165

N/A

0.345DataRank · unranked

9 citations

Florence Pasquier, Christophe Marzac, Eric Deconinck, Carlotta Caterina Damanti, Gwendoline Leroy +10 more

Update of variants identified in the pancreatic β-cell KATPchannel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes

Yearbook of pediatric endocrinology(2020)10.1530/ey.17.2.11

N/A

0.104DataRank · unranked

1 citations

Cécile Saint‐Martin, Klaus Brusgaard, Knight Johnson, Lydia Aguilar‐Bryan, Pamela Bowman +15 more

Update of variants identified in the pancreatic β‐cell K ATP channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes

Human Mutation(2020)10.1002/humu.23995

N/A

0DataRank · unranked

175 citations

Cécile Saint‐Martin, Klaus Brusgaard, Amy E. Knight Johnson, Lydia Aguilar‐Bryan, Pamela Bowman +15 more

Biological behaviors of mutant proinsulin contribute to the phenotypic spectrum of diabetes associated with insulin gene mutations

Molecular and Cellular Endocrinology(2020)10.1016/j.mce.2020.111025

N/A

0DataRank · unranked

18 citations

Cécile Saint‐Martin, Jialu Xu, Li Ding, Ruodan Wang, Wenli Feng +9 more