🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Patrick Hanna

Harvard University

ORCID: 0000-0002-4998-2901

Also affiliated with Massachusetts General Hospital

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 7 papers. Top paper: “Targeted Long-Read Sequencing Identifies a Retrotransposon Insertion as a Cause of Altered GNAS Exon A/B Methylation in a Family With Autosomal Dominant Pseudohypoparathyroidism Type 1b (PHP1B)”.

Targeted Long-Read Sequencing Identifies a Retrotransposon Insertion as a Cause of Altered GNAS Exon A/B Methylation in a Family With Autosomal Dominant Pseudohypoparathyroidism Type 1b (PHP1B)

Journal of Bone and Mineral Research(2020)10.1002/jbmr.4647
N/A
0DataRank · unranked
29 citations

Patrick Hanna, Miranda Galey, Monica Reyes, Agnès Linglart, Evan E. Eichler +2 more

Progression of PTH Resistance in Autosomal Dominant Pseudohypoparathyroidism Type Ib Due to Maternal STX16 Deletions

The Journal of Clinical Endocrinology & Metabolism(2021)10.1210/clinem/dgab660
N/A
0DataRank · unranked
14 citations

Monica Reyes, Patrick Hanna, Anu Sharma, Terry J. DeClue, Robert C. Olney +3 more

A Novel Familial PHP1B Variant With Incomplete Loss of Methylation at GNAS-A/B and Enhanced Methylation at GNAS-AS2

The Journal of Clinical Endocrinology & Metabolism(2021)10.1210/clinem/dgab136
N/A
0DataRank · unranked
10 citations

Bruno Francou, Brigitte Delemer, Harald Jüppner, Agnès Linglart, Patrick Hanna

Lack of GNAS Remethylation During Oogenesis May Be a Cause of Sporadic Pseudohypoparathyroidism Type Ib

The Journal of Clinical Endocrinology & Metabolism(2021)10.1210/clinem/dgab830
N/A
0DataRank · unranked
8 citations

Monica Reyes, Patrick Hanna, Zentaro Kiuchi, Serap Turan, Daniel Zeve +11 more

Substantially Delayed Maturation of Growth Plate Chondrocytes in “Humanized” PTH1R Mice with the H223R Mutation of Jansen's Disease

JBMR Plus(2023)10.1002/jbm4.10802
N/A
0DataRank · unranked
11 citations

Damla Firat, Patrick Hanna, Mohd Golam Quader Khan, Michael Bruce, Maria Shvedova +5 more

Homozygous Ser-1 to Pro-1 mutation in parathyroid hormone identified in hypocalcemic patients results in secretion of a biologically inactive pro-hormone

Proceedings of the National Academy of Sciences(2023)10.1073/pnas.2208047120
N/A
0DataRank · unranked
6 citations

Ashok Khatri, Shawn Choi, Séverine Brabant, Matti L. Gild, Marie Piketty +8 more

A mouse model of Jansen’s metaphyseal chondrodysplasia for investigating disease mechanisms and candidate therapeutics

Proceedings of the National Academy of Sciences(2025)10.1073/pnas.2500176122
N/A
0DataRank · unranked
6 citations

Damla Firat, Mohd Parvez-Khan, Monica Reyes, Patrick Hanna, Prem Swaroop Yadav +12 more