Population-based screening for breast and ovarian cancer risk due to<i>BRCA1</i>and<i>BRCA2</i>

Efrat Gabai-Kapara, Amnon Lahad, Bella Kaufman, +13

Proceedings of the National Academy of Sciences

Transgenic expression of human acetylcholinesterase induces progressive cognitive deterioration in mice

Rachel Beeri, Christian Andrés, Efrat Lev-Lehman, +4

Current Biology

Neurodegenerative DiseasesAlzheimer's DiseaseMedicineTransgenic ExpressionDegenerative Pathology +8

Enhanced Hemicholinium Binding and Attenuated Dendrite Branching in Cognitively Impaired Acetylcholinesterase‐Transgenic Mice

Rachel Beeri, Nicolas Le Novère, Ronald F. Mervis, +4

Journal of Neurochemistry

Acetylcholinesterase-transgenic mice display embryonic modulations in spinal cord choline acetyltransferase and neurexin Iβ gene expression followed by late-onset neuromotor deterioration

Christian Andrés, Rachel Beeri, Alon Friedman, +5

Proceedings of the National Academy of Sciences

A role for<i>TENM1</i>mutations in congenital general anosmia

Anna Alkelai, Tsviya Olender, Rebecca Haffner‐Krausz, +12

Clinical Genetics

Neurobiological MechanismDevelopmental BiologyMolecular NeuroscienceMendelian DisorderSynapse Organization +13

X-inactivation in Fabry disease

Deborah Elstein, Ella Schachamorov, Rachel Beeri, +1

Gene

Fabry DiseaseMendelian DisorderGenetic DisorderPathogenesisPathology +2

Population screening for BRCA1/BRCA2 founder mutations in Ashkenazi Jews: proactive recruitment compared with self-referral

Sari Lieberman, Ariela Tomer, Avi Ben-Chetrit, +14

Genetics in Medicine

Functional variant of KLOTHO: a breast cancer risk modifier among BRCA1 mutation carriers of Ashkenazi origin

Ingo Wolf, Yael Laitman, Tamar Rubinek, +11

Oncogene

OncologyEngineeringCancer RiskOncogenic AgentMedicine +12

Egr-1 upregulates the Alzheimer's disease presenilin-2 gene in neuronal cells

Paul Renbaum, Rachel Beeri, Efrat Gabai, +4

Gene

Alzheimer's DiseaseAutophagyCell DeathNeuroprotectionNeurology +7

Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and Surveillance

Sari Lieberman, Tom Walsh, Menachem Schechter, +15

Gastroenterology

Allelic VariantGenetic DisorderGeneticsClinical GeneticsHuman Polymorphism +4