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Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

Scientific reports, 2017-06, Vol.7 (1), p.3715-8, Article 3715

2017

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Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis

PloS one, 2018-01, Vol.13 (1), p.e0190601-e0190601

2018

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ACE I/D polymorphism and epidemiological findings for COVID-19: One year after the pandemic outbreak in Europe

The Journal of infection, 2021-09, Vol.83 (3), p.381-412

2021

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Pharmacogenomics of Multiple Sclerosis: A Systematic Review

Frontiers in neurology, 2019-02, Vol.10, p.134

2019

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CCR5 Δ32 and CTLA-4 +49 A/G Gene Polymorphisms and Interferon-β Treatment Response in Croatian and Slovenian Multiple Sclerosis Patients

International journal of molecular sciences, 2024-07, Vol.25 (13), p.7412

2024

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Association between Insertion-Deletion Polymorphism of the Angiotensin-Converting Enzyme Gene and Treatment Response to Antipsychotic Medications: A Study of Antipsychotic-Naïve First-Episode Psychosis Patients and Nonadherent Chronic Psychosis Patients

International journal of molecular sciences, 2022-10, Vol.23 (20), p.12180

2022

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Gantenerumab reduces amyloid-β plaques in patients with prodromal to moderate Alzheimer's disease: a PET substudy interim analysis

Alzheimer's research & therapy, 2019-12, Vol.11 (1), p.101-101, Article 101

2019

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Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes

Scientific reports, 2019-06, Vol.9 (1), p.9171-10, Article 9171

2019

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Could the CCR5-Δ32 Mutation be Protective in SARS-CoV-2 Infection?

Physiological research, 2021-12, Vol.70 (Suppl 2), p.S249-S252

2021

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The Influence of Hemochromatosis Gene (HFE) Mutations on SARS-CoV-2 Susceptibility and COVID-19 Severity

Balkan medical journal, 2023-05, Vol.40 (3), p.229-231

2023

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In reply

Croatian medical journal, 2021-06, Vol.62 (3), p.305-306

2021

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In reply

Croatian medical journal, 2021-06, Vol.62 (3), p.305-306

2021

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GiOPARK Project: The Genetic Study of Parkinson's Disease in the Croatian Population

Genes, 2024-02, Vol.15 (2), p.255

2024

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The impact of ACE gene I/D polymorphism on plasma glucose and lipid concentrations in schizophrenia patients

Psychiatry research, 2015-05, Vol.227 (1), p.71-72

2015

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Potential protective role of a NOD2 polymorphism in the susceptibility to multiple sclerosis is not associated with interferon therapy

Biomedical reports, 2021-12, Vol.15 (6), p.1-100, Article 100

2021

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Does the CCR5-Δ32 mutation explain the variable coronavirus-2019 pandemic statistics in Europe?

Croatian medical journal, 2020-12, Vol.61 (6), p.525-526

2020

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The insertion/deletion polymorphism in the angiotensin-converting enzyme gene and nicotine dependence in schizophrenia patients

Journal of Neural Transmission, 2017-04, Vol.124 (4), p.511-518

2017

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Chronic iron overload induces gender-dependent changes in iron homeostasis, lipid peroxidation and clinical course of experimental autoimmune encephalomyelitis

Neurotoxicology (Park Forest South), 2016-12, Vol.57, p.1-12

2016

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Lack of association between C282Y and H63D polymorphisms in the hemochromatosis gene and risk of multiple sclerosis: A meta-analysis

Biomedical reports, 2022-02, Vol.16 (2), p.12-12, Article 12

2022

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Association between the ACE-I/D polymorphism and nicotine dependence amongst patients with lung cancer

Biomedical reports, 2020-12, Vol.13 (6), p.58-1

2020

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Angiotensin-converting enzyme insertion/deletion gene polymorphism in multiple sclerosis: a meta-analysis

Neurological sciences, 2016-12, Vol.37 (12), p.1955-1959

2016

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MMP-2 −1575G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?

Journal of neuroimmunology, 2015-09, Vol.286, p.13-15

2015

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MMP-2 − 1575 G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?

Journal of neuroimmunology, 2015-09, Vol.286, p.13-15

2015

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RELATIONSHIP BETWEEN VASCULAR PATHOLOGY AT BASELINE AND AMYLOID-RELATED IMAGING ABNORMALITIES (ARIA) IN PRODROMAL AD PATIENT POPULATION IN SCARLET ROAD STUDY

Alzheimer's & dementia, 2017-07, Vol.13 (7), p.P254-P254

2017

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CORRELATION BETWEEN BASELINE VASCULAR PATHOLOGY/RISK FACTORS AND PROGRESSION OF ALZHEIMER'S DISEASE IN A PRODROMAL POPULATION

Alzheimer's & dementia, 2017-07, Vol.13 (7), p.P255-P255

2017

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Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis

ACE I/D polymorphism and epidemiological findings for COVID-19: One year after the pandemic outbreak in Europe

Pharmacogenomics of Multiple Sclerosis: A Systematic Review

CCR5 Δ32 and CTLA-4 +49 A/G Gene Polymorphisms and Interferon-β Treatment Response in Croatian and Slovenian Multiple Sclerosis Patients

Association between Insertion-Deletion Polymorphism of the Angiotensin-Converting Enzyme Gene and Treatment Response to Antipsychotic Medications: A Study of Antipsychotic-Naïve First-Episode Psychosis Patients and Nonadherent Chronic Psychosis Patients

Gantenerumab reduces amyloid-β plaques in patients with prodromal to moderate Alzheimer's disease: a PET substudy interim analysis

Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes

Could the CCR5-Δ32 Mutation be Protective in SARS-CoV-2 Infection?

The Influence of Hemochromatosis Gene (HFE) Mutations on SARS-CoV-2 Susceptibility and COVID-19 Severity

In reply

In reply

GiOPARK Project: The Genetic Study of Parkinson's Disease in the Croatian Population

The impact of ACE gene I/D polymorphism on plasma glucose and lipid concentrations in schizophrenia patients

Potential protective role of a NOD2 polymorphism in the susceptibility to multiple sclerosis is not associated with interferon therapy

Does the CCR5-Δ32 mutation explain the variable coronavirus-2019 pandemic statistics in Europe?

The insertion/deletion polymorphism in the angiotensin-converting enzyme gene and nicotine dependence in schizophrenia patients

Chronic iron overload induces gender-dependent changes in iron homeostasis, lipid peroxidation and clinical course of experimental autoimmune encephalomyelitis

Lack of association between C282Y and H63D polymorphisms in the hemochromatosis gene and risk of multiple sclerosis: A meta-analysis

Association between the ACE-I/D polymorphism and nicotine dependence amongst patients with lung cancer

Angiotensin-converting enzyme insertion/deletion gene polymorphism in multiple sclerosis: a meta-analysis

MMP-2 −1575G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?

MMP-2 − 1575 G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?

RELATIONSHIP BETWEEN VASCULAR PATHOLOGY AT BASELINE AND AMYLOID-RELATED IMAGING ABNORMALITIES (ARIA) IN PRODROMAL AD PATIENT POPULATION IN SCARLET ROAD STUDY

CORRELATION BETWEEN BASELINE VASCULAR PATHOLOGY/RISK FACTORS AND PROGRESSION OF ALZHEIMER'S DISEASE IN A PRODROMAL POPULATION

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