Get started
Author

Kelin Chen

Observed names: Chen, Kelin, KELIN CHEN
ORCID: 0000-0002-3086-1667
Observed ORCID: 0000-0002-3086-1667
OpenAlex ID: A5081555026
The hospital Israelita Albert Einstein standards for constitutional sequence variants classification: version 2023
2023 · Caio Robledo D’Angioli Costa Quaio, José Ricardo Magliocco Ceroni, et al. · Human Genomics · 11
PDF
ACMG secondary findings in the Brazilian rare genomes project: insights from 5402 genome sequencing
2025 · Eduardo Perrone, Luiza Virmond, et al. · Journal of Human Genetics · 5
PDF
Whole Genome Sequencing for the Diagnosis of Rare Disorders
2025 · Antonio Victor Campos Coelho, Rafael Sales de Albuquerque, et al. · medRxiv · 1
PDF
Assessment of diagnostic yield and clinical utility of genome sequencing in critically ill infants
2026 · Carolina A. Moreno, Marina de França, et al. · Pediatric Research
Transthyretin Amyloidosis: Does more than one pathogenic variant confer higher severity? PC75 (#478)
2024 · Larissa Bruscky, Edileide de, et al.
Sustained Ventricular Tachycardia as an isolated feature of transthyretin amyloidotic cardiomyopathy - Val50Met PB43 (#476)
2024 · Larissa Bruscky, Edileide de, et al.
Transthyretin amyloidosis in the second decade of life: a rare genetic variant PB18 (#524)
2024 · Plínio José, EDILEIDE CORREIA, et al.
Additional file 1 of The hospital Israelita Albert Einstein standards for constitutional sequence variants classification: version 2023
2023 · Quaio, Caio Robledo D’Angioli Costa, Ceroni, José Ricardo Magliocco, et al. · Figshare
Taquicardia Ventricular Sustentada como Apresentação Isolada de Cardiomiopatia Amiloidótica por Transtirretina - Val50Met
2021 · Edileide de Barros Correia, Larissa Ventura Ribeiro Bruscky, et al. · ABC Heart Failure & Cardiomyopathy
PDF
Works count: 10
Citation count: 17
H-index: 2
I10-index: 1
Year
Topic
Type