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Lurbinectedin Is Active in Patients With BRCA1/2 Mutant Breast Cancer

Cancer Discovery
Oncology
2018English

Recurrent, Activating Variants in the Receptor Tyrosine Kinase DDR2 Cause Warburg-Cinotti Syndrome

American Journal of Human Genetics
Genetics
2018English

Cancer Mutations Occur Frequently in Normal Esophageal Epithelium

Cancer Discovery
Oncology
2018English

JAMA Oncology

JAMA Oncology
Cancer ResearchOncology
2018English

Age-Related Changes in HAPLN1 Increase Lymphatic Permeability and Affect Routes of Melanoma Metastasis

Cancer Discovery
Oncology
2018English

Germline De Novo Mutations in ATP1A1 Cause Renal Hypomagnesemia, Refractory Seizures, and Intellectual Disability

American Journal of Human Genetics
Genetics
2018English

Detecting Expansions of Tandem Repeats in Cohorts Sequenced With Short-Read Sequencing Data

American Journal of Human Genetics
Genetics
2018English

Highlights

JAMA Oncology
Cancer ResearchOncology
2018English

Human Models Are Needed for Studying Human Neurodevelopmental Disorders

American Journal of Human Genetics
Genetics
2018English

The Genetic Landscape of Diamond-Blackfan Anemia

American Journal of Human Genetics
Genetics
2018English

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