Ida Vanessa Doederlein Schwartz is an expert in Genetics at Hospital de Clínicas de Porto Alegre (Brazil). As of October 2026, ScienceLeadR ranks Ida Vanessa Doederlein Schwartz in the top 1% of experts worldwide for Lipid Metabolism Disorders, Metabolism, Inborn Errors and Brain Diseases, Metabolic. Ida Vanessa Doederlein Schwartz has authored 373 publications, the most recent in 2026, and is an investigator in 3 clinical trials. SLR score: 1,113 (community average: 125). How the SLR is computed.

LeadR Profile

Ida Vanessa Doederlein Schwartz Hospital de Clínicas de Porto Alegre Brazil
1 113 ScienceLeadR Reputation 1113
Network Map

Genetics

Subspecialties: Biochemistry - Neurology - Public Health

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Organizations

Career arc: 2000 - 2026

Source: PubMed

Hospital de Clínicas de Porto Alegre

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 373

Citations

Citations: 6 744 1st author: 26 Last author: 181 Unique author: 0


Breakdown by type

Click a legend label to hide or show it in the chart.

Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Insights into morbidity and mortality in Gaucher disease: a cohort study.
PMID 42927298 — comorbidity, mortality, neoplasms, cohort studies, cause of death, sepsis, morbidity, therapeutics, gaucher disease
Mol Genet Metab Rep20260
International Guideline on the Diagnosis, Treatment, and Monitoring of Long-Chain Fatty Acid Oxidation Disorders (LC-FAOD).
PMID 42779363 — muscular diseases, fasting, neonatal screening, stress, physiological, work, diagnosis, therapeutics, fatty acids
J Inherit Metab Dis20261
Rare diseases in Brazil: a nationwide analysis of the diagnostic odyssey.
PMID 42742802 — rare diseases, diagnosis
J Community Genet20260
Cobalamin-Related Remethylation Disorders: Pregnancy Outcomes and Prenatal Treatment-New Cases and a Literature Study.
PMID 42644808 — pregnancy, mothers, safety, pregnancy outcome, metabolism, inborn errors, hydroxocobalamin, therapeutics, fetus, neurodevelopment
J Inherit Metab Dis20260
Glucose Transporter Deficiency Syndrome Type 1 (Glut1-DS): New Insights From a Brazilian Cohort of Patients.
PMID 42638834 — glucose transport proteins, facilitative, developmental disabilities, phenotype, diet, movement disorders, diet, ketogenic, movement
JIMD Rep20260

Clinical Studies 3

Sources: ClinicalTrials, EU CTIS

Synthesis

By phase:

N/A 2
Phase 3 1

By status:

Recruiting 2
Completed 1

By type:

Observational 2
Interventional 1

By Monocentric/Multicentric:

monocentric 1
multicentric2to4 0
multicentric5to9 0
multicentricup10 2

Main Topics

LeadR Networks

Main global connection map