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Loop profile: 1672102

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Employment (5)

Foundation for Research and Technology Hellas: Heraklion, GR

2019-03-01 to present | Genetics data analyst (Institure of Computer Sciences, Information Systems Laboratory)
Employment
Source: Self-asserted source
Helen Latsoudis

Foundation for Research and Technology Hellas: Heraklion, GR

2015-05 to 2019-02-28 | Research fellow (Institute of Molecular Biology and Biotechnology, Post-Genomics Laboratory)
Employment
Source: Self-asserted source
Helen Latsoudis

University of Crete School of Medicine: Heraklion, GR

2013-05 to 2015-04 | Research fellow (Internal Medicine)
Employment
Source: Self-asserted source
Helen Latsoudis

University of Crete School of Medicine: Heraklion, GR

2011-03 to 2012-06 | Post-doctoral Research Fellow (Pharmacology)
Employment
Source: Self-asserted source
Helen Latsoudis

University of Crete School of Medicine: Heraklion, GR

2004-01 to 2011-02 | Post-doctoral Research Fellow (Neurology)
Employment
Source: Self-asserted source
Helen Latsoudis

Education and qualifications (3)

King’s College London: London, GB

1998 to 2003 | PhD in Genetics
Education
Source: Self-asserted source
Helen Latsoudis

King’s College London: London, GB

1997 to 1998 | MSc in Neurosciences
Education
Source: Self-asserted source
Helen Latsoudis

King’s College London: London, GB

1993 to 1997 | BSc in Clinical Sciences
Education
Source: Self-asserted source
Helen Latsoudis

Works (24)

Perspectives for the Use of Umbilical Cord Blood in Transplantation and Beyond: Initiatives for an Advanced and Sustainable Public Banking Program in Greece

Journal of Clinical Medicine
2024-02-18 | Journal article
DOI: 10.3390/jcm13041152
Contributors: Patra Pateraki; Helen Latsoudis; Anastasia Papadopoulou; Ioanna Gontika; Irene Fragiadaki; Irene Mavroudi; Nikoleta Bizymi; Aristea Batsali; Michail Klontzas; Angeliki Xagorari et al.
Source: check_circle
Crossref
grade
Preferred source (of 2)‎

Study of Alzheimer's disease- and frontotemporal dementia-associated genes in the Cretan Aging Cohort.

Neurobiology of aging
2022-07-11 | Journal article
DOI: 10.1016/j.neurobiolaging.2022.07.002
PMID: 36117051
Contributors: Helen Latsoudis
Source: Self-asserted source
Helen Latsoudis

Dent-2 disease with a Bartter-like phenotype caused by the Asp631Glu mutation in the OCRL gene.

BMC nephrology
2022-05-12 | Journal article
DOI: 10.1186/s12882-022-02812-9
PMID: 35549682
PMC: PMC9097321
Contributors: Helen Latsoudis
Source: Self-asserted source
Helen Latsoudis

Significance of regional population HLA immunogenetic datasets in the efficacy of umbilical cord blood banks and marrow donor registries: a study of Cretan HLA genetic diversity

Cytotherapy
2022-02 | Journal article
DOI: 10.1016/j.jcyt.2021.07.010
Contributors: Helen Latsoudis; Emmanouil Stylianakis; Irene Mavroudi; Alexandros Kanterakis; Pavlos Pavlidis; Anthie Georgopoulou; Aristea Batsali; Ioanna Gontika; Irene Fragiadaki; Maria Zamanakou et al.
Source: check_circle
Crossref

Detection of the novel HLA-B*51:232:02 variant in an inhabitant from the island of Crete.

HLA
2020-12-01 | Journal article
DOI: 10.1111/tan.14157
PMID: 33241916
Source: Self-asserted source
Helen Latsoudis

Two novel HLA-A alleles, HLA-A*03:399 and -A*24:17:01:02, detected in inhabitants from the island of Crete

HLA
2020-12-01 | Journal article
DOI: 10.1111/tan.14156
PMID: 33241918
Source: Self-asserted source
Helen Latsoudis

Two novel HLA-C alleles, HLA-C*15:228 and -C*04:434, detected in inhabitants from the island of Crete.

HLA
2020-12-01 | Journal article
DOI: 10.1111/tan.14155
PMID: 33241910
Source: Self-asserted source
Helen Latsoudis

Genetic cause of heterogeneous inherited myopathies in a cohort of Greek patients.

Molecular genetics and metabolism reports
2020-11-30 | Journal article
DOI: 10.1016/j.ymgmr.2020.100682
PMID: 33304817
PMC: PMC7711282
Source: Self-asserted source
Helen Latsoudis

Detection of the novel HLA-DQB1*03:439 variant in an inhabitant from the island of Crete.

HLA
2020-11-08 | Journal article
DOI: 10.1111/tan.14125
PMID: 33124770
Source: Self-asserted source
Helen Latsoudis

Two novel HLA-DRB1 alleles detected in inhabitants from the island of Crete.

HLA
2020-11-08 | Journal article
DOI: 10.1111/tan.14126
PMID: 33124731
Source: Self-asserted source
Helen Latsoudis
grade
Preferred source (of 2)‎

Differential Expression of miR-4520a Associated With Pyrin Mutations in Familial Mediterranean Fever (FMF).

Journal of cellular physiology
2016-12-20 | Journal article
DOI: 10.1002/jcp.25602
PMID: 27636101
Source: Self-asserted source
Helen Latsoudis

The odyssey of a young gene: structure-function studies in human glutamate dehydrogenases reveal evolutionary-acquired complex allosteric regulation mechanisms.

Neurochemical research
2014-02-11 | Journal article
DOI: 10.1007/s11064-014-1251-0
PMID: 24515454
Source: Self-asserted source
Helen Latsoudis

The human GLUD2 glutamate dehydrogenase and its regulation in health and disease.

Neurochemistry international
2011-03-21 | Journal article
DOI: 10.1016/j.neuint.2011.03.015
PMID: 21420458
Source: Self-asserted source
Helen Latsoudis

Gain-of-function variant in GLUD2 glutamate dehydrogenase modifies Parkinson's disease onset.

European journal of human genetics : EJHG
2009-10-14 | Journal article
DOI: 10.1038/ejhg.2009.179
PMID: 19826450
PMC: PMC2987208
Source: Self-asserted source
Helen Latsoudis

Human GLUD1 and GLUD2 glutamate dehydrogenase localize to mitochondria and endoplasmic reticulum.

Biochemistry and cell biology = Biochimie et biologie cellulaire
2009-06-01 | Journal article
DOI: 10.1139/o09-008
PMID: 19448744
Source: Self-asserted source
Helen Latsoudis

Mutations in human GLUD2 glutamate dehydrogenase affecting basal activity and regulation.

Journal of neurochemistry
2009-05-01 | Journal article
DOI: 10.1111/j.1471-4159.2009.05914.x
PMID: 19393024
Source: Self-asserted source
Helen Latsoudis

The human GLUD2 glutamate dehydrogenase: localization and functional aspects.

Neurochemistry international
2009-03-13 | Journal article
DOI: 10.1016/j.neuint.2009.03.001
PMID: 19428807
Source: Self-asserted source
Helen Latsoudis

A8344G tRNALys mutation associated with recurrent brain stem stroke-like episodes.

Journal of neurology
2009-02-27 | Journal article
DOI: 10.1007/s00415-009-0921-3
PMID: 19253012
Source: Self-asserted source
Helen Latsoudis

Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism.

Parkinsonism & related disorders
2008-10-26 | Journal article
DOI: 10.1016/j.parkreldis.2008.09.001
PMID: 18952485
PMC: PMC2749264
Source: Self-asserted source
Helen Latsoudis

Mitochondrial DNA polymorphisms and haplogroups in Parkinson's disease and control individuals with a similar genetic background.

Journal of human genetics
2008-02-20 | Journal article
DOI: 10.1007/s10038-008-0259-1
PMID: 18286226
Source: Self-asserted source
Helen Latsoudis

Novel mutation of the PRNP gene of a clinical CJD case.

BMC infectious diseases
2006-11-27 | Journal article
DOI: 10.1186/1471-2334-6-169
PMID: 17129366
PMC: PMC1693557
Source: Self-asserted source
Helen Latsoudis

LRRK2 mutations on Crete: R1441H associated with PD evolving to PSP.

Neurology
2006-10-01 | Journal article
DOI: 10.1212/01.wnl.0000239829.33936.73
PMID: 17060595
Source: Self-asserted source
Helen Latsoudis

Patients with horizontal gaze palsy and progressive scoliosis due to ROBO3 E319K mutation have both uncrossed and crossed central nervous system pathways and perform normally on neuropsychological testing.

Journal of neurology, neurosurgery, and psychiatry
2006-06-13 | Journal article
DOI: 10.1136/jnnp.2006.088435
PMID: 16772357
PMC: PMC2077731
Source: Self-asserted source
Helen Latsoudis

Mutation screening and association analysis of the parkin gene in Parkinson's disease patients from South-West China.

European neurology
2003-01-01 | Journal article
DOI: 10.1159/000068505
PMID: 12584415
Source: Self-asserted source
Helen Latsoudis
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