Martin Procházka

Martin Procházka

Univerzita Palackého v Olomouci

H-index: 25

Europe-Czech Republic

About Martin Procházka

Martin Procházka, With an exceptional h-index of 25 and a recent h-index of 16 (since 2020), a distinguished researcher at Univerzita Palackého v Olomouci, specializes in the field of lékařství.

His recent articles reflect a diverse array of research interests and contributions to the field:

Reply to: Questioning the cycad theory of Kii ALS–PDC causation

Prenatal detection of copy number variants in fetuses with detected congenital devolpmental disordes, from 2015 to 2020 by Multiplex Ligation-Dependent Probe Amplification and …

Endemic parkinsonism: clusters, biology and clinical features

Prenatálny záchyt CNV variant u plodov so zachytenými vrodenými vývojovými poruchami, v období od 2015–2020 metódami MLPA a microarray.

Ovarian tumors and genetic predisposition.

Detection of unknown and rare pathogenic variants in antithrombin, protein C and protein S deficiency using high-throughput targeted sequencing

Whole exome sequencing study in isolated south-eastern Moravia (Czechia) population indicates heterogenous genetic background for parkinsonism development

Karyotyping of lymphocytes and epithelial cells of distinct embryonic origin does not help to predict the Turner syndrome features

Martin Procházka Information

University

Position

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Citations(all)

2282

Citations(since 2020)

1000

Cited By

1605

hIndex(all)

25

hIndex(since 2020)

16

i10Index(all)

58

i10Index(since 2020)

26

Email

University Profile Page

Univerzita Palackého v Olomouci

Google Scholar

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Martin Procházka Skills & Research Interests

lékařství

Top articles of Martin Procházka

Title

Journal

Author(s)

Publication Date

Reply to: Questioning the cycad theory of Kii ALS–PDC causation

Katerina Menšíková

Raymond Rosales

Carlo Colosimo

Peter Spencer

Annie Lannuzel

...

2024/2/9

Prenatal detection of copy number variants in fetuses with detected congenital devolpmental disordes, from 2015 to 2020 by Multiplex Ligation-Dependent Probe Amplification and …

Ceska Gynekologie

Štefeková Andrea

Čapková Pavlína

Curtisová Václava

Mracká Enghjargalan

Filipová Hana

...

2023/1/1

Endemic parkinsonism: clusters, biology and clinical features

Katerina Menšíková

John C Steele

Raymond Rosales

Carlo Colosimo

Peter Spencer

...

2023/10

Prenatálny záchyt CNV variant u plodov so zachytenými vrodenými vývojovými poruchami, v období od 2015–2020 metódami MLPA a microarray.

Česká gynekologie

Andrea Štefeková

Pavlína Čapková

Václava Curtisová

Enkhjargalan Mracká

Hana Filipová

...

2023/6/21

Ovarian tumors and genetic predisposition.

Ceska Gynekologie

Štellmachová Júlia

Vrtěl Petr

Vrtěl Radek

Janíková Mária

Kolaříková Kristýna

...

2022/1/1

Detection of unknown and rare pathogenic variants in antithrombin, protein C and protein S deficiency using high-throughput targeted sequencing

Diagnostics

Petr Vrtel

Ludek Slavik

Radek Vodicka

Julia Stellmachova

Martin Prochazka

...

2022/4/23

Whole exome sequencing study in isolated south-eastern Moravia (Czechia) population indicates heterogenous genetic background for parkinsonism development

Frontiers in Neuroscience

Kristyna Kolarikova

Radek Vodicka

Radek Vrtel

Julia Stellmachova

Martin Prochazka

...

2022/3/17

Karyotyping of lymphocytes and epithelial cells of distinct embryonic origin does not help to predict the Turner syndrome features

Hormone Research in Paediatrics

Jan Pavlicek

Ondrej Soucek

Radek Vrtel

Eva Klaskova

Vaclav Hana

...

2022/11/11

Haplotype analysis of the X chromosome in patients with Turner syndrome in order to verify the possible effect of imprinting on selected symptoms

Biomedical Papers

Petr Vrtel

Radek Vrtel

Eva Klaskova

Dita Vrbicka

Katerina Adamova

...

2022/3/1

Reply: Matters Arising ‘Lewy body disease or diseases with Lewy bodies?’

npj Parkinson's Disease

Kateřina Menšíková

Radoslav Matěj

Carlo Colosimo

Raymond Rosales

Lucie Tučková

...

2022/6/23

High-Throughput Sequencing Haplotype Analysis Indicates in LRRK2 Gene a Potential Risk Factor for Endemic Parkinsonism in Southeastern Moravia, Czech …

Life

Kristyna Kolarikova

Radek Vodicka

Radek Vrtel

Julia Stellmachova

Martin Prochazka

...

2022/1/14

MLPA analysis of 32 foetuses with a congenital heart defect and 1 foetus with renal defects--pilot study. The significant frequency rate of presented pathological CNV.

Biomedical Papers of the Medical Faculty of Palacky University in Olomouc

Andrea Stefekova

Pavlina Capkova

Zuzana Capkova

Vaclava Curtisova

Josef Srovnal

...

2022/6/1

Lewy body disease or diseases with Lewy bodies?

Kateřina Menšíková

Radoslav Matěj

Carlo Colosimo

Raymond Rosales

Lucie Tučková

...

2022/1/10

Nádory ovaria a genetická dispozice.

Česká gynekologie

Zuzana Zachari

Júlia Štellmachová

Petr Vrtěl

Radek Vrtěl

Mária Janíková

...

2022/5/10

Reflexe vyjednávání homosexuální identity mezi čínskými migranty v České republice

Martin Procházka

2021/9/6

Cytoplasmic transfer improves human egg fertilization and embryo quality: an evaluation of sibling oocytes in women with low oocyte quality

Reproductive Sciences

Ales Sobek

Emil Tkadlec

Eva Klaskova

Martin Prochazka

2021/5

Fetal heart rhabdomyomatosis: a single-center experience

The Journal of Maternal-Fetal & Neonatal Medicine

Jan Pavlicek

Eva Klaskova

Sabina Kapralova

Martin Prochazka

Radek Vrtel

...

2021/3/4

Quality of life and sexuality in women with urinary incontinence.

Ceska Gynekologie

Pičmanová Petra

Procházka Martin

2021/1/1

Nepravidelné polohy a porodní mechanismy

Štěpánka Bubeníčková

Martin Procházka

Kateřina Janoušková

Renata Hrubá

Jozef Záhumenský

...

2020

The contribution of X-chromosome genomic imprinting to the bicuspid aortic valve and aortic coarctation prevalence in women with Turner syndrome

European Heart Journal

E Klaskova

P Vrtel

R Vrtel

K Adamova

DITA Vrbicka

...

2020/11

See List of Professors in Martin Procházka University(Univerzita Palackého v Olomouci)