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

Alexander A.L. Jorge

Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo

ORCID: 0000-0003-2567-7360

MedicineBiochemistry, 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 8 papers. Top paper: “High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency”.

High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.06.013

N/A

0.612DataRank · unranked

58 citations

Cathy Smith, Hironori Bando, Alexander A.L. Jorge, Denise Rockstroh-Lippold, Sebastián Vishnopolska +29 more

DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2024.12.012

N/A

0.292DataRank · unranked

6 citations

Anja Barešić, Iván K. Chinn, Jonathan May, Anu Goenka, Kate Chandler +91 more

High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency

medRxiv(2021)10.1101/2021.02.04.21249469

N/A

0DataRank · unranked

1 citations

Cathy Smith, Hironori Bando, Alexander A.L. Jorge, Denise Rockstroh-Lippold, Sebastián Vishnopolska +28 more

Diagnosis of TBC1D32‐associated conditions: Expanding the phenotypic spectrum of a complex ciliopathy

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63150

N/A

0DataRank · unranked

7 citations

Karen Chong, David Chitayat, Kelly L. Gilmore, Alexander A.L. Jorge, Bruna Lucheze Freire +10 more

Homozygous CDH2 variant may be associated with hypopituitarism without neurological disorders

Endocrine Connections(2023)10.1530/ec-22-0473

N/A

0DataRank · unranked

4 citations

João Madeira, Péter Gergics, Renata Kertsz, Juliana Moreira Marques, Nicholas Silvestre de Souza Trigueiro +15 more

Contributions of Common Genetic Variants to Constitutional Delay of Puberty and Idiopathic Hypogonadotropic Hypogonadism

The Journal of Clinical Endocrinology & Metabolism(2024)10.1210/clinem/dgae166

N/A

0DataRank · unranked

7 citations

Evan C Schafer, Anna A Hindman, Wei He, Raja Brauner, Angela Delaney +18 more

DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders

UNC Libraries(2025)10.17615/dy6f-xt03

N/A

0DataRank · unranked

0 citations

Benjamin Cogné, Rachel Rabin, E Kessler, Céline Chappé, Melanie Brügger +92 more

Allelic Variants in Established Hypopituitarism Genes Expand Our Knowledge of the Phenotypic Spectrum

Genes(2021)10.3390/genes12081128

N/A

0DataRank · unranked

1 citations

Nathalia Garcia Bianchi Pereira Ferreira, Anna Benedetti, Mariana Cotarelli Madi, Juliana Moreira Silva, Jun Z. Li +14 more