Helena Hůlková

3.2k citations

51 papers · 1.5k indexed · h-index 20

Co-authors: M. Elleder Robert J. Desnick Martin G. Bialer Donna L. Bernstein Stanislav Kmoch J Zeman Veronika Barešová Helena Jahnová
Topics: Lysosomal Storage Disorders Research (24 papers)Cellular transport and secretion (14 papers)Mitochondrial Function and Pathology (8 papers)
Cited by: Physiology Nephrology
Journals: Journal of Clinical Investigation Neurology Cell Metabolism
Partner nations: Czechia United States Germany

In The Last Decade

Helena Hůlková

50 papers receiving 1.5k citations

Peers

Countries citing papers authored by Helena Hůlková

Since Specialization

Citations

This map shows the geographic impact of Helena Hůlková's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Helena Hůlková with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Helena Hůlková more than expected).

Fields of papers citing papers by Helena Hůlková

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Helena Hůlková. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Helena Hůlková. The network helps show where Helena Hůlková may publish in the future.

Co-authorship network of co-authors of Helena Hůlková

This figure shows the co-authorship network connecting the top 25 collaborators of Helena Hůlková. A scholar is included among the top collaborators of Helena Hůlková based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Helena Hůlková. Helena Hůlková is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Transcript, protein, metabolite and cellular studies in skin fibroblasts demonstrate variable pathogenic impacts of NPC1 mutations 2020 ·Orphanet Journal of Rare Diseases ·(unknown),(unknown),Ladislav Kuchař,Ondřej Lukšan,Befekadu Asfaw,Hana Vlášková,(unknown),(unknown),Helena Poupětová,Helena Jahnová,Helena Hůlková,J. Ledvinová,Lenka Dvořáková,Jakub Sikora,M Jirsa,Marie T. Vanier,Martin Hřebı́ček	4
2	Changes in Transcription Pattern Lead to a Marked Decrease in COX, CS and SQR Activity After the Developmental Point of the 22nd Gestational Week 2018 ·Physiological Research ·(unknown),(unknown),(unknown),Hana Hansíková,Helena Hůlková,V. Šmíd,J Zeman,Tomáš Honzík,Markéta Tesařová	4
3	Autosomal Dominant Tubulointerstitial Kidney Disease Due to MUC1 Mutation 2017 ·American Journal of Kidney Diseases ·Samuel Mon-Wei Yu,Anthony J. Bleyer,(unknown),Leal Herlitz,Martina Živná,Helena Hůlková,Glen S. Markowitz,Belinda Jim	8
4	Observational, retrospective study of a large cohort of patients with Niemann-Pick disease type C in the Czech Republic: a surprisingly stable diagnostic rate spanning almost 40 years 2014 ·Orphanet Journal of Rare Diseases ·Helena Jahnová,Lenka Dvořáková,Hana Vlášková,Helena Hůlková,Helena Poupětová,Martin Hřebı́ček,Pavel Ješina	45
5	Mutation of Nogo-B Receptor, a Subunit of cis-Prenyltransferase, Causes a Congenital Disorder of Glycosylation 2014 ·Cell Metabolism ·Eon Joo Park,Kariona A. Grabińska,Ziqiang Guan,Viktor Stránecký,Hana Hartmannová,Kateřina Hodaňová,Veronika Barešová,Jana Sovová,Levente József,Nina Ondrušková,Hana Hansíková,Tomáš Honzík,J Zeman,Helena Hůlková,Rong Wen,Stanislav Kmoch,William C. Sessa	99
6	Rapid Isolation of Lysosomal Membranes from Cultured Cells 2013 ·Folia Biologica ·(unknown),J. Lukáš,(unknown),(unknown),Eva Svobodová,Ladislav Kuchař,(unknown),Helena Hůlková,J. Ledvinová,Martin Hřebı́ček	2
7	Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis 2013 ·European Journal of Human Genetics ·Blanka Stibůrková,Ivan Šebesta,Kimiyoshi Ichida,Makiko Nakamura,Helena Hůlková,Vladimír Krylov,(unknown),Helena Jahnová	50
8	Systemic AL amyloidosis with unusual cutaneous presentation unmasked by carotenoderma 2013 ·Amyloid ·Helena Hůlková,(unknown),(unknown),(unknown),J. Hanuš,(unknown),Miroslav Souček,Ivana Márová,Josef Feit,Iva Staniczková Zambo,(unknown),Hana Vlášková,(unknown),Petr Novák,Zdeněk Kostrouch,M. Elleder	1
9	Glycosphingolipid profile of the apical pole of human placental capillaries: The relevancy of the observed data to Fabry disease 2012 ·Glycobiology ·Helena Hůlková,J. Ledvinová,Ladislav Kuchař,F. Šmíd,(unknown),M. Elleder	7
10	Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis 2011 ·The American Journal of Human Genetics ·Lenka Nosková,Viktor Stránecký,Hana Hartmannová,Anna Přistoupilová,Veronika Barešová,Robert Ivánek,Helena Hůlková,Helena Jahnová,Julie van der Zee,John F. Staropoli,Katherine B. Sims,Jaana Tyynelä,Christine Van Broeckhoven,Peter C.G. Nijssen,Sara Mole,M. Elleder,Stanislav Kmoch	10
11	Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis 2011 ·The American Journal of Human Genetics ·Lenka Nosková,Viktor Stránecký,Hana Hartmannová,Anna Přistoupilová,Veronika Barešová,Robert Ivánek,Helena Hůlková,Helena Jahnová,Julie van der Zee,John F. Staropoli,Katherine B. Sims,Jaana Tyynelä,Christine Van Broeckhoven,Peter C.G. Nijssen,Sara Mole,M. Elleder,Stanislav Kmoch	201
12	Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone 2010 ·Clinical Nephrology ·Anthony J. Bleyer,Martina Živná,Helena Hůlková,Kateřina Hodaňová,Petr Vyleťal,Jakub Sikora,J Živný,Jana Sovová,Thomas C. Hart,Jacqueline Adams,M. Elleder,Karin S. Kapp,Robert Haws,Lynn D. Cornell,Stanislav Kmoch,P. Suzanne Hart	30
13	Loss of function of Sco1 and its interaction with cytochrome c oxidase 2009 ·American Journal of Physiology-Cell Physiology ·Lukáš Stibůrek,Kateřina Veselá,Hana Hansı́ková,Helena Hůlková,J Zeman	83
14	Structural analysis of tissues affected by cytochrome C oxidase deficiency due to mutations in the SCO2 gene 2008 ·Apmis ·Kateřina Veselá,Helena Hůlková,Hana Hansíková,J Zeman,M. Elleder	14
15	Atypical CLN2 with later onset and prolonged course: a neuropathologic study showing different sensitivity of neuronal subpopulations to TPP1 deficiency 2008 ·Acta Neuropathologica ·M. Elleder,Lenka Dvořáková,(unknown),Hana Vlášková,Helena Hůlková,Rastislav Druga,Helena Poupětová,(unknown),(unknown)	29
16	Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome 2006 ·Kidney International ·Petr Vyleťal,(unknown),Marie Hubálek Kalbáčová,Kateřina Hodaňová,Veronika Barešová,Blanka Stibůrková,Jakub Sikora,Helena Hůlková,J Živný,Jacek Majewski,Anne Simmonds,J. P. Fryns,Gopalakrishnan Venkat‐Raman,M. Elleder,Stanislav Kmoch	89
17	Lactosylceramide in lysosomal storage disorders. A comparative immunohistochemical and biochemical study 2005 ·Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin ·Helena Hůlková,J. Ledvinová,Befekadu Asfaw,(unknown),Karel Kopřiva,M. Elleder	11
18	Mapping of a new candidate locus for uromodulin-associated kidney disease (UAKD) to chromosome 1q41 2005 ·Kidney International ·Kateřina Hodaňová,Jacek Majewski,(unknown),Petr Vyleťal,Marie Hubálek Kalbáčová,Blanka Stibůrková,Helena Hůlková,Marie‐Christine Chagnon,(unknown),Anthony M. Marinaki,Jean‐Pierre Fryns,Gopalakrishnan Venkat‐Raman,Stanislav Kmoch	26
19	Prosaposin Deficiency - a Rarely Diagnosed, Rapidly Progressing, Neonatal Neurovisceral Lipid Storage Disease. Report of a Further Patient 2005 ·Neuropediatrics ·M. Elleder,(unknown),(unknown),Martin Hřebı́ček,Linda Berná,J. Ledvinová,Helena Hůlková,Hendrik Rosewich,(unknown),Barbara C. Paton,K. Harzer	40
20	[Various manifestations of the A8344G mtDNA heteroplasmic mutation in 4 families with the MERRF syndrome]. 1999 ·PubMed ·(unknown),J Zeman,H Houst'ková,Hana Hansíková,(unknown),Helena Hůlková,M. Elleder,Evžen Růžička,(unknown),Eva Hrubá,J Houštěk	8

About Helena Hůlková

Helena Hůlková is a scholar working on Clinical Biochemistry, Cell Biology and Physiology, having authored 51 papers that have together received 1.5k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (24 papers), Cellular transport and secretion (14 papers) and Mitochondrial Function and Pathology (8 papers). The work is most often cited by research in Physiology (179 citations), Physiology (692 citations) and Nephrology (163 citations). Helena Hůlková has collaborated with scholars based in Czechia, United States and Germany. Frequent co-authors include M. Elleder, Robert J. Desnick, Martin G. Bialer, Donna L. Bernstein, Stanislav Kmoch, J Zeman, Veronika Barešová, Helena Jahnová, Viktor Stránecký and Hana Hartmannová. Their work appears in journals such as Journal of Clinical Investigation, Neurology and Cell Metabolism.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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