Jesús Argente

Also affiliated with Instituto de Salud Carlos III, Hospital Infantil Universitario Niño Jesús, Hospital Universitario de La Princesa, IMDEA Food, Universidad Autónoma de Madrid

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 6 papers. Top paper: “Efficacy and safety of setmelanotide, a melanocortin-4 receptor agonist, in patients with Bardet-Biedl syndrome and Alström syndrome: a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial with an open-label period”.

Efficacy and safety of setmelanotide, a melanocortin-4 receptor agonist, in patients with Bardet-Biedl syndrome and Alström syndrome: a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial with an open-label period

The Lancet Diabetes & Endocrinology(2022)10.1016/s2213-8587(22)00277-7

N/A

4.0DataRank · unranked

188 citations

Wendy K. Chung, Hélène Dollfus, Robert Haws, Gabriel Ángel Martos‐Moreno, Christine Poitou +7 more

The Congenital and Acquired Mechanisms Implicated in the Etiology of Central Precocious Puberty

Endocrine Reviews(2022)10.1210/endrev/bnac020

N/A

0.691DataRank · unranked

99 citations

Ana Pinheiro Machado Canton, Carlos Eduardo Seraphim, Ana Paula Abreu, Delanie B. Macedo, Berenice B. Mendonça +4 more

Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy

Nature Communications(2022)10.1038/s41467-022-34349-8

N/A

0DataRank · unranked

42 citations

John J. Reynolds, Farid Ullah, Bertrand Isidor, Robert F. Shearer, Xénia Latypova +43 more

Molecular basis of normal and pathological puberty: from basic mechanisms to clinical implications

The Lancet Diabetes & Endocrinology(2023)10.1016/s2213-8587(22)00339-4

N/A

0DataRank · unranked

77 citations

Leo Dunkel, Ursula B Kaiser, Ana Cláudia Latronico, Alejandro Lomniczi, Leandro Soriano‐Guillén +2 more

Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype–phenotype correlations and common mechanisms

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63247

N/A

0DataRank · unranked

41 citations

Justin Blair, Batsal Devkota, Sierra Fortunato, Dinah Clark, Audrey Lawrence +92 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