Karin Weiss
Karin Weiss is an expert in Genetics at Rambam Health Care Campus (Israel). Karin Weiss has authored 76 publications, the most recent in 2026. SLR score: 228 (community average: 125). How the SLR is computed.
LeadR Profile
Genetics
Subspecialties: Endocrinology - Pediatrics - Biochemistry
Main Topics
Publications and Clinical Studies
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Organizations
Career arc: 2007 - 2026
Number : 76
Citations
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Latest Publications
5 most recent indexed articles
Source: Pubmed
| Title | Journal | Year | Citations |
|---|---|---|---|
| A New Case of Lethal Congenital Contracture Syndrome Type 3 With Hyperinsulinism and Optic Atrophy. PMID 42747333 — atrophy, optic atrophy, contracture, hyperinsulinism, arthrogryposis, clubfoot, infant | Clin Genet | 2026 | 0 |
| CCDC149: a novel gene associated with hypopituitarism and neurodevelopmental impairment. PMID 42554577 — genes, growth, neuroendocrinology, brain, hypopituitarism, phenotype, hormones, pedigree, neurodevelopment | Eur J Endocrinol | 2026 | 0 |
| Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from parkinsonism to perinatal lethality. PMID 41986367 — genes, mitochondrial membranes, parkinsonian disorders, phenotype, proteasome endopeptidase complex, membranes | Nat Commun | 2026 | 0 |
| Pseudohypoxia and Family History Are Key Predictors of Severe Outcomes in Hereditary Pheochromocytoma and Paraganglioma Syndromes. PMID 41783997 — genes, paraganglioma, pheochromocytoma, predictive value of tests, hormones, risk factors, diagnosis, catecholamines, learning, history | Eur J Endocrinol | 2026 | 0 |
| Impact of Rapid Exome Sequencing on Pediatric Patients With Cardiomyopathy and Acute Heart Failure. PMID 41572441 — heart failure, heart, myocarditis, diagnosis, exome, therapeutics, cardiomyopathies | Am J Med Genet A | 2026 | 0 |
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