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Publications by Erica Hasten

Tbx1 and Foxi3 Genetically Interact in the Pharyngeal Pouch Endoderm in a Mouse Model for 22q11.2 Deletion Syndrome

PLoS Genetics
EvolutionEcologyGeneticsMolecular BiologyCancer ResearchSystematicsBehavior
2019English

Related publications

Complement Activation in 22q11.2 Deletion Syndrome

Journal of Clinical Immunology
AllergyImmunology
2020English

Schizophrenia and 22q11.2 Deletion Syndrome

Current Psychiatry Reports
PsychiatryMental Health
2008English

Aberrant Cortical Morphometry in the 22q11.2 Deletion Syndrome

Biological Psychiatry
Biological Psychiatry
2015English

Hematological Abnormalities and 22q11.2 Deletion Syndrome

Revista Brasileira de Hematologia e Hemoterapia
2011English

Acute Dystonia in a Patient With 22q11.2 Deletion Syndrome

Mental Illness
PsychiatryMental Health
2015English

Obesity in Adults With 22q11.2 Deletion Syndrome

Genetics in Medicine
MedicineGenetics
2016English

Primary Amenorrhea and Absent Uterus in the 22q11.2 Deletion Syndrome

American Journal of Medical Genetics, Part A
Genetics
2007English

22q11.2 Deletion Syndrome-Associated Parkinson's Disease

Movement Disorders Clinical Practice
Neurology
2018English

Candidate Modifier Genes for Immune Function in 22q11.2 Deletion Syndrome

Molecular genetics & genomic medicine
GeneticsMolecular Biology
2019English

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