Raja Brauner

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 3 papers. Top paper: “TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal loci”.

TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal loci

Human Molecular Genetics(2020)10.1093/hmg/ddaa120

N/A

0DataRank · unranked

22 citations

Ravikumar Balasubramanian, Zachary A Kupchinsky, David L. Keefe, Lacey Plummer, Kamal Khan +19 more

Familial central precocious puberty due to DLK1 deficiency: novel genetic findings and relevance of serum DLK1 levels

European Journal of Endocrinology(2023)10.1093/ejendo/lvad129

N/A

0DataRank · unranked

17 citations

Carlos Eduardo Seraphim, Flávia Rezende Tinano, Maiara Ribeiro Piovesan, Ana Pinheiro Machado Canton, Ken McElreavey +11 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