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GEORGIA KARADIMA

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Greece

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Chromosomes, Human, Pair 21

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Georgios Koutsis; Marios Panas; A Pandraud; M M Reilly; N W Wood; Paraskewi Floroskufi; GEORGIA KARADIMA; H Houlden
Mutational analysis of PMP22, EGR2, LITAF and NEFL in Greek Charcot-Marie-Tooth type 1 patients.
Georgios Koutsis; GEORGIA KARADIMA; Athina Kladi; Marios Panas
The challenge of juvenile Huntington disease: to test or not to test.
GEORGIA KARADIMA; Georgios Koutsis; Christina Dimovasili; Demetris Vassilopoulos; Marios Panas
Age at onset in Huntington's disease: replication study on the association of HAP1.

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All Publications

2013: Georgios Koutsis; Marios Panas; A Pandraud; M M Reilly; N W Wood; Paraskewi Floroskufi; GEORGIA KARADIMA; H Houlden
Mutational analysis of PMP22, EGR2, LITAF and NEFL in Greek Charcot-Marie-Tooth type 1 patients.
Clinical genetics 2013;83(4):388-91.
2013: Georgios Koutsis; GEORGIA KARADIMA; Athina Kladi; Marios Panas
The challenge of juvenile Huntington disease: to test or not to test.
Neurology 2013;80(11):990-6.
2012: GEORGIA KARADIMA; Georgios Koutsis; Christina Dimovasili; Demetris Vassilopoulos; Marios Panas
Age at onset in Huntington's disease: replication study on the association of HAP1.
Parkinsonism & related disorders 2012;18(9):1027-8.
2012: Georgios Koutsis; Henry Houlden; GEORGIA KARADIMA; A Pandraud; R Paudel; Mary G Sweeney; Nicholas W Wood; Marios Panas
Genetic screening of Greek patients with Huntington’s disease phenocopies identifies an SCA8 expansion.
Journal of neurology 2012;259(9):1874-8.
2012: Georgios Koutsis; Marios Panas; Amelie Pandraud; James M Polke; Nicholas W Wood; GEORGIA KARADIMA; Henry Houlden
Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot-Marie-Tooth disease.
Brain : a journal of neurology 2012;135(Pt 8):e217, 1-6; author reply e218, 1-2.
2011: Marios Panas; Evangelos Vassos; K Christodoulou; Nikolaos Kalfakis; GEORGIA KARADIMA; Athina Kladi; Dimitrios Vassilopoulos
Huntington's disease in Greece: the experience of 14 years.
Clinical genetics 2011;80(6):586-90.
2011: GEORGIA KARADIMA; Georgios Koutsis; Paraskewi Floroskufi; Dimitrios Vassilopoulos; Marios Panas
Mutational analysis of PMP22, GJB1 and MPZ in Greek Charcot-Marie-Tooth type 1 neuropathy patients.
Clinical genetics 2011;80(5):497-9.
2011: Catherine Sarri; Virginia Theodorou; Zeynep Tümer; Kirstine Ravn; Theologia Sarafidou; Sofia Douzgou; Maria Grigoriadou; Yolanda Gyftodimou; GEORGIA KARADIMA; Haris Kokotas; Harry Kontos; Nicholas K Moschonas; Effie Pandelia; A Pasparaki; Michael B Petersen
Complex distal 10q rearrangement in a girl with mild intellectual disability: follow up of the patient and review of the literature of non-acrocentric satellited chromosomes.
American journal of medical genetics. Part A 2011;155A(11):2841-54.
2011: Marios Panas; Nikolaos Kalfakis; GEORGIA KARADIMA; Dimitris Vassilopoulos
Hereditary neuropathy unmasked by levofloxacin.
The Annals of pharmacotherapy 2011;45(10):1312-3.
2011: Georgios Koutsis; Paraskewi Floroskufi; GEORGIA KARADIMA; Constantinos Sfagos; Demetris Vassilopoulos; Marios Panas
The rs10492972 KIF1B polymorphism and disease progression in Greek patients with multiple sclerosis.
Journal of neurology 2011;258(9):1726-8.
2011: Marios Panas; Nikolaos Kalfakis; GEORGIA KARADIMA; Dimitris Vassilopoulos
Co-segregation of Huntington disease and hereditary spastic paraplegia in 4 generations.
The neurologist 2011;17(4):211-2.
2009: Georgios Koutsis; Marios Panas; E Giogkaraki; GEORGIA KARADIMA; Constantinos Sfagos; Dimitrios Vassilopoulos
An APOA1 promoter polymorphism is associated with cognitive performance in patients with multiple sclerosis.
Multiple sclerosis (Houndmills, Basingstoke, England) 2009;15(2):174-9.
2008: M Panas; GEORGIA KARADIMA; M Markianos; N Kalfakis; D Vassilopoulos
Phenotypic discordance in a pair of monozygotic twins with Huntington's disease.
Clinical genetics 2008;74(3):291-2.
2008: Thomas Zambelis; Marios Panas; Panagiotis Kokotis; GEORGIA KARADIMA; Evangelia Kararizou; Nikos Karandreas
Central motor and sensory pathway involvement in an X-linked Charcot-Marie-Tooth family.
Acta neurologica Belgica 2008;108(2):44-7.
2007: Paraskewi Floroskufi; Marios Panas; GEORGIA KARADIMA; Dimitrios Vassilopoulos
New mutation of the MPZ gene in a family with the Dejerine-Sottas disease phenotype.
Muscle & nerve 2007;35(5):667-9.
2007: Georgios Koutsis; Marios Panas; GEORGIA KARADIMA; Dimitris Mandellos; Constantinos Sfagos; Constantin Potagas; Dimitrios Vassilopoulos
APOE genotypes in Greek multiple sclerosis patients: no effect on the MS Severity Score.
Journal of neurology 2007;254(3):394-5.
2007: Georgios Koutsis; Marios Panas; E Giogkaraki; Constantin Potagas; GEORGIA KARADIMA; Constantinos Sfagos; Dimitrios Vassilopoulos
APOE epsilon4 is associated with impaired verbal learning in patients with MS.
Neurology 2007;68(8):546-9.
2006: Dimitris G Dikeos; George N Papadimitriou; Daniel Souery; Jurgen Del-Favero; Isabelle Massat; Douglas Blackwood; Sven Cichon; Eugenia G Daskalopoulou; Sladjana Ivezic; RAdka Kaneva; GEORGIA KARADIMA; Cristina Lorenzi; vihra milanova; Walter Muir; Markus M Nöthen; Lilijana Oruc; Marcella Rietschel; Alessandro Serretti; Christine Van Broeckhoven; Constantin R Soldatos; Costas N Stefanis; Julien Mendlewicz
Lack of genetic association between the phospholipase A2 gene and bipolar mood disorder in a European multicentre case-control study.
Psychiatric genetics 2006;16(4):169-71.
2006: GEORGIA KARADIMA; Marios Panas; Paraskewi Floroskufi; Nikolaos Kalfakis; Dimitrios Vassilopoulos
Four novel connexin 32 mutations in X-linked Charcot-Marie-Tooth disease with phenotypic variability.
Journal of neurology 2006;253(2):263-4.
2004: Marios Panas; GEORGIA KARADIMA; Nikolaos Kalfakis; Paraskewi Floroskufi; Dimitrios Vassilopoulos
Charcot-Marie-Tooth disease type 1A with central nervous system involvement in two generations.
Journal of neurology 2004;251(4):484-5.
2004: GEORGIA KARADIMA; Marios Panas; Paraskewi Floroskufi; Nikolaos Kalfakis; Dimitrios Vassilopoulos
A V38A mutation in X-linked Charcot-Marie-Tooth neuropathy with unusual clinical features.
Journal of neurology 2004;251(2):222-3.
2003: George N Papadimitriou; Dimitris G Dikeos; Daniel Souery; Jurgen Del-Favero; Isabelle Massat; Dimitrios Avramopoulos; Sylvie Blairy; Sven Cichon; Sladjana Ivezic; RAdka Kaneva; GEORGIA KARADIMA; Roberta Lilli; vihra milanova; Markus M Nöthen; Lilijana Oruc; Marcella Rietschel; Alessandro Serretti; Christine Van Broeckhoven; Costas N Stefanis; Julien Mendlewicz
Genetic association between the phospholipase A2 gene and unipolar affective disorder: a multicentre case-control study.
Psychiatric genetics 2003;13(4):211-20.
2002: Nikolaos Kalfakis; Marios Panas; GEORGIA KARADIMA; Paraskewi Floroskufi; Nikos Kokolakis; Dimitrios Vassilopoulos
Hereditary neuropathy with liability to pressure palsies emerging during vincristine treatment.
Neurology 2002;59(9):1470-1.
2002: Marios Panas; Nikolaos Kalfakis; GEORGIA KARADIMA; Panagiota Davaki; Dimitrios Vassilopoulos
Friedreich's ataxia mimicking hereditary motor and sensory neuropathy.
Journal of neurology 2002;249(11):1583-6.
2001: George N Papadimitriou; Dimitris G Dikeos; GEORGIA KARADIMA; Dimitrios Avramopoulos; Eugenia G Daskalopoulou; Costas N Stefanis
GABA-A receptor beta3 and alpha5 subunit gene cluster on chromosome 15q11-q13 and bipolar disorder: a genetic association study.
American journal of medical genetics 2001;105(4):317-20.
2001: George N Papadimitriou; Dimitris G Dikeos; Eugenia G Daskalopoulou; GEORGIA KARADIMA; Dimitrios Avramopoulos; C Contis; Costas N Stefanis
Association between GABA-A receptor alpha 5 subunit gene locus and schizophrenia of a later age of onset.
Neuropsychobiology 2001;43(3):141-4.
2000: Marios Panas; GEORGIA KARADIMA; Nikolaos Kalfakis; O Psarrou; P Floroskoufi; Athina Kladi; Michael B Petersen; Dimitrios Vassilopoulos
Genotyping of presenilin-1 polymorphism in amyotrophic lateral sclerosis.
Journal of neurology 2000;247(12):940-2.
2000: G Dean; N C Nevin; M Mikkelsen; GEORGIA KARADIMA; M B Petersen; M Kelly; J O'Sullivan
Investigation of a cluster of children with Down's syndrome born to mothers who had attended a school in Dundalk, Ireland.
Occupational and environmental medicine 2000;57(12):793-804.
2000: Michael B Petersen; GEORGIA KARADIMA; M Samaritaki; Dimitrios Avramopoulos; Dimitrios Vassilopoulos; M Mikkelsen
Association between presenilin-1 polymorphism and maternal meiosis II errors in Down syndrome.
American journal of medical genetics 2000;93(5):366-72.
2000: Gotthold Barbi; Ingo Kennerknecht; Gudrun Wöhr; Dimitrios Avramopoulos; GEORGIA KARADIMA; Michael B Petersen
Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotype.
American journal of medical genetics 2000;91(2):116-22.
2000: Aspasia Tsezou; Sophia Kitsiou-Tzeli; Angeliki Galla; Michael B Petersen; GEORGIA KARADIMA; Maria Syrrou; S Sahlèn; Elisabeth Blennow
Molecular cytogenetic characterization and origin of two de novo duplication 9p cases.
American journal of medical genetics 2000;91(2):102-6.
1999: Dimitris G Dikeos; George N Papadimitriou; Dimitrios Avramopoulos; GEORGIA KARADIMA; Eugenia G Daskalopoulou; Daniel Souery; Julien Mendlewicz; Dimitrios Vassilopoulos; Costas N Stefanis
Association between the dopamine D3 receptor gene locus (DRD3) and unipolar affective disorder.
Psychiatric genetics 1999;9(4):189-95.
1999: Marios Panas; Dimitrios Avramopoulos; GEORGIA KARADIMA; Michael B Petersen; Dimitrios Vassilopoulos
Apolipoprotein E and presenilin-1 genotypes in Huntington's disease.
Journal of neurology 1999;246(7):574-7.
1999: Jolanda Gyftodimou; GEORGIA KARADIMA; Effie Pandelia; Dimitrios Vassilopoulos; Michael B Petersen
Angelman syndrome with uniparental disomy due to paternal meiosis II nondisjunction.
Clinical genetics 1999;55(6):483-6.
1999: Catherine Dacou-Voutetakis; Amalia Sertedaki; M Maniatis-Christidis; Catherine Sarri; GEORGIA KARADIMA; Michael B Petersen; Athina Xaidara; Maria Kanariou; Polyxeni Nicolaidou
Insulin dependent diabetes mellitus (IDDM) and autoimmune thyroiditis in a boy with a ring chromosome 18: additional evidence of autoimmunity or IDDM gene(s) on chromosome 18.
Journal of medical genetics 1999;36(2):156-8.
1998: GEORGIA KARADIMA; Merete Bugge; P Nicolaidis; Dimitrios Vassilopoulos; Dimitrios Avramopoulos; Maria Grigoriadou; Beate Albrecht; Eberhard Passarge; Göran Annerén; Elisabeth Blennow; Niels Clausen; Angeliki Galla-Voumvouraki; Aspasia Tsezou; Sophia Kitsiou-Tzeli; Johanne M D Hahnemann; Jens Michael Hertz; Gunnar Houge; M Kuklík; Milan Macek Jr.; D Lacombe; K Miller; A Moncla; I López Pajares; Philippos C Patsalis; Michael B Petersen
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism.
European journal of human genetics : EJHG 1998;6(5):432-8.
1998: Marie-Claude Potier; A Dutriaux; R Orti; Jürgen Groet; Nathalie Gibelin; GEORGIA KARADIMA; G Lutfalla; A Lynn; Christine Van Broeckhoven; Aravinda Chakravarti; M Petersen; Dean Nizetic; Jean-Maurice Delabar; Jean Rossier
Two sequence-ready contigs spanning the two copies of a 200-kb duplication on human 21q: partial sequence and polymorphisms.
Genomics 1998;51(3):417-26.
1998: A R Savage; Michael B Petersen; DL Pettay; Lisa F Taft; K Allran; Sallie B Freeman; GEORGIA KARADIMA; Dimitrios Avramopoulos; Claudine P Torfs; M Mikkelsen; Terry J Hassold; Stephanie L Sherman
Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans.
Human molecular genetics 1998;7(8):1221-7.
1998: George N Papadimitriou; Dimitris G Dikeos; GEORGIA KARADIMA; Dimitrios Avramopoulos; Eugenia G Daskalopoulou; Dimitrios Vassilopoulos; Costas N Stefanis
Association between the GABA(A) receptor alpha5 subunit gene locus (GABRA5) and bipolar affective disorder.
American journal of medical genetics 1998;81(1):73-80.
1998: P Nicolaidis; G von Beust; Merete Bugge; GEORGIA KARADIMA; Dimitrios Vassilopoulos; Karen Brøndum-Nielsen; Michael B Petersen
Analysis of the origin of the extra chromosome in trisomy 8 in 4 cases of spontaneous abortions.
Fetal diagnosis and therapy 1998;13(1):42-5.
1997: E Sklavounou; Effrosini Economou-Petersen; GEORGIA KARADIMA; Marios Panas; Dimitrios Avramopoulos; A Varsou; Dimitrios Vassilopoulos; Michael B Petersen
Apolipoprotein E polymorphism in the Greek population.
Clinical genetics 1997;52(4):216-8.
1997: Neil E Lamb; Eleanor Feingold; A Savage; Dimitrios Avramopoulos; S Freeman; Y Gu; A Hallberg; J Hersey; GEORGIA KARADIMA; DL Pettay; D Saker; J Shen; Lisa F Taft; M Mikkelsen; Michael B Petersen; Terry J Hassold; Stephanie L Sherman
Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21.
Human molecular genetics 1997;6(9):1391-9.