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Ghadir Elias-Assad

Observed names: Elias-Assad, G., Gadhir Elias-Assad, Ghadir Elias Assad, Ghadir Elias-assad
Institution: Bar-Ilan University
ORCID: 0000-0003-4892-9292
Observed ORCID: 0000-0003-4892-9292
OpenAlex ID: A5058452686
Long-Term Follow-Up and Outcomes of Autoimmune Thyroiditis in Childhood
2020 · Osnat Admoni, Shoshana Rath, et al. · Frontiers in Endocrinology · 26
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The evolving role of whole-exome sequencing in the management of disorders of sex development
2021 · Yardena Tenenbaum-Rakover, Osnat Admoni, et al. · Endocrine Connections · 23
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Case Report: Neonatal Diabetes Mellitus Caused by a Novel GLIS3 Mutation in Twins
2021 · Shira London, Elisa De Franco, et al. · Frontiers in Endocrinology · 23
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High Prevalence of Hearing Impairment in Primary Congenital Hypothyroidism
2020 · Tal Almagor, Shoshana Rath, et al. · European Thyroid Journal · 16
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Persistent Müllerian Duct Syndrome Caused by a Novel Mutation of an Anti-MüIlerian Hormone Receptor Gene: Case Presentation and Literature Review.
2016 · Ghadir Elias-Assad, Marwan Elias, et al. · PubMed · 14
Maturity onset diabetes of the young type 2 (MODY2): Insight from an extended family
2021 · Ghadir Elias-Assad, Raunak Saab, et al. · Diabetes Research and Clinical Practice · 11
Long-Term Outcome of Patients with TPO Mutations
2021 · Leraz Tobias, Ghadir Elias-Assad, et al. · Journal of Clinical Medicine · 7
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Case Report: Severe Hypocalcemic Episodes Due to Autoimmune Enteropathy
2021 · Inbal Halabi, Marie Noufi Barohom, et al. · Frontiers in Endocrinology · 6
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The natural course of newborns with transient congenital hypothyroidism
2024 · Tal Almagor, Shlomo Almashanu, et al. · Endocrine Connections · 2
Clinical and Molecular Characteristics and Long-term Follow-up of Children With Pseudohypoparathyroidism Type IA
2023 · Hanna Ludar, Yael Levy-Shraga, et al. · The Journal of Clinical Endocrinology & Metabolism · 2
OR15-07 Novel Genes Involved in Sex Differentiation Identified by Whole-Exome Sequencing in a Cohort of Children with Disorders of Sex Development
2020 · Yardena Tenenbaum Rakover, Osnat Admoni, et al. · Journal of the Endocrine Society · 1
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Neonatal Diabetes Mellitus Caused by a Novel GLIS3 Mutation in Twins
2018 · Shira London, Ghadir Elias-Assad, et al. · 57th Annual ESPE · 1
CCDC149 : a novel gene associated with hypopituitarism and neurodevelopmental impairment
2026 · Louise C Gregory, Shoshana Rath, et al. · European Journal of Endocrinology
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Low-level mosaic variants causing the pancreatic disease congenital hyperinsulinism can be detected from blood DNA
2026 · Jasmin J. Bennett, Thomas W. Laver, et al. · EBioMedicine
SAT-023 Recessive truncations in CCDC149, a previously uncharacterized gene, are a novel cause of Congenital Hypopituitarism.
2025 · Louise Cheryl Gregory, Shoshana Rath, et al. · Journal of the Endocrine Society
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Recessive truncations in a previously uncharacterized gene, CCDC149, are a novel cause of congenital hypopituitarism
2025 · Louise Gregory, Shoshana Rath, et al. · Endocrine Abstracts
Supplementary Material for: High Prevalence of Hearing Impairment in Primary Congenital Hypothyroidism
2020 · Almagor, T., Rath, S., et al. · Figshare
The Evolving Role of Whole Exome Sequencing in the Diagnosis of Disorders of Sex Development (DSD)
2019 · Yardena Tenenbaum‐Rakover, Osnat Admoni, et al. · 58th Annual ESPE Meeting (ESPE 2019)
Clinical Characteristics and Long-Term Follow-Up of Patients with Congenital Hypothyroidism (CH) due to Thyroid Peroxidase (TPO) Gene Mutations
2019 · Leraz Tobias, Tal Almagor, et al. · 58th Annual ESPE Meeting (ESPE 2019)
Hearing Loss Among Patients with Congenital Hypothyroidism
2018 · Tal Almagor, Dan Nachtigal, et al. · 57th Annual ESPE
A Novel Mutation of Anti-Mullerian Hormone Receptor Gene in a Male with Persistent Mullerian Duct Syndrome
2015 · Ghadir Elias-Assad, Marwan Elias, et al. · 54th Annual ESPE
Works count: 21
Citation count: 132
H-index: 7
I10-index: 6
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