Kirsi Huoponen

5.3k citations

49 papers · 3.4k indexed · 1 hit paper · h-index 27

Co-authors: Marja‐Liisa Savontaus Eeva Nikoskelainen Douglas C. Wallace M L Savontaus Tarja Lamminen Antonio Torroni Vesa Juvonen Rosaria Scozzari
Topics: Mitochondrial Function and Pathology (20 papers)Metabolism and Genetic Disorders (16 papers)Amino Acid Enzymes and Metabolism (11 papers)
Cited by: Clinical Biochemistry Biochemistry Ophthalmology
Journals: Nature Genetics Genetics Biochemical and Biophysical Research Communications
Partner nations: Finland United States Italy

In The Last Decade

Kirsi Huoponen

49 papers receiving 3.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Classification of European mtDNAs From an Analysis of Three European Populations

1996 670 citations Kirsi Huoponen, Marja‐Liisa Savontaus et al. profile →

Peers

Countries citing papers authored by Kirsi Huoponen

Since Specialization

Citations

This map shows the geographic impact of Kirsi Huoponen'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 Kirsi Huoponen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kirsi Huoponen more than expected).

Fields of papers citing papers by Kirsi Huoponen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kirsi Huoponen. 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 Kirsi Huoponen. The network helps show where Kirsi Huoponen may publish in the future.

Co-authorship network of co-authors of Kirsi Huoponen

This figure shows the co-authorship network connecting the top 25 collaborators of Kirsi Huoponen. A scholar is included among the top collaborators of Kirsi Huoponen 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 Kirsi Huoponen. Kirsi Huoponen 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	Carnitine deficiency and l-carnitine supplementation in lysinuric protein intolerance 2008 ·Metabolism ·Laura M. Tanner,Kirsti Näntö‐Salonen,Mohamed S. Rashed,(unknown),M. Aalto,(unknown),Harri Niinikoski,Kirsi Huoponen,Olli Simell	15
2	Migration Waves to the Baltic Sea Region 2008 ·Annals of Human Genetics ·Tuuli Lappalainen,Virpi H. Laitinen,Elina Salmela,Peter M. Andersen,Kirsi Huoponen,M L Savontaus,Päivi Lahermo	53
3	Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions 2007 ·Genetics in Medicine ·(unknown),Sirpa Ala‐Mello,Carola Saloranta,Maila Penttinen,Minna Pöyhönen,Kirsi Huoponen,Wiktor Borozdin,Birke Bausch,Elke Botzenhart,Christian Wilhelm,Helena Kääriäinen,Jürgen Kohlhase	38
4	Heterodimerization of y+LAT-1 and 4F2hc visualized by acceptor photobleaching FRET microscopy 2007 ·Biochimica et Biophysica Acta (BBA) - Biomembranes ·(unknown),(unknown),Juha Mykkänen,Olli Simell,Kirsi Huoponen,Kaisa M. Heiskanen	7
5	Two alternative promoters regulate the expression of lysinuric protein intolerance gene SLC7A7 2006 ·Molecular Genetics and Metabolism ·(unknown),Olli Simell,Kirsi Huoponen,Juha Mykkänen	12
6	Identification of an X-Chromosomal Locus and Haplotype Modulating the Phenotype of a Mitochondrial DNA Disorder 2005 ·The American Journal of Human Genetics ·Gavin Hudson,Sharon Keers,Patrick Yu Wai Man,Philip G. Griffiths,Kirsi Huoponen,Marja-Liisa Savontaus,Eeva Nikoskelainen,Massimo Zeviani,Franco Carrara,Rita Horváth,Veronika Karcagi,Liesbeth Spruijt,I.F.M. de Coo,Hubert J.M. Smeets,Patrick F. Chinnery	144
7	Dominant optic atrophy: correlation between clinical and molecular genetic studies 2005 ·Acta Ophthalmologica Scandinavica ·(unknown),Kirsi Huoponen,Maija Mäntyjärvi,(unknown),(unknown),Eeva‐Marja Sankila,Marja‐Liisa Savontaus,Mirja Somer,Eeva Nikoskelainen	46
8	New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2) 2004 ·Neuromuscular Disorders ·Riitta Sallinen,Anna Vihola,Linda L. Bachinski,Kirsi Huoponen,Hannu Haapasalo,Peter Hackman,Shaozeng Zhang,Mario Sirito,Hannu Kalimo,G. Meola,Nina Horelli‐Kuitunen,Maija Wessman,Ralf Krahe,Bjarne Udd	37
9	Tandem repeats and length variation in the mitochondrial DNA control region ofEpirrita autumnata(Lepidoptera: Geometridae) 2002 ·Genome ·(unknown),Kirsi Huoponen,M.-L. Savontaus,Kai Ruohomäki	17
10	Expression of Normal and Mutant GFP-Tagged y+L Amino Acid Transporter-1 in Mammalian Cells 2002 ·Biochemical and Biophysical Research Communications ·(unknown),Juha Mykkänen,Perttì Aula,Olli Simell,Marja‐Liisa Savontaus,Kirsi Huoponen	15
11	Mitochondrial DNA variation in an Aboriginal Australian population: evidence for genetic isolation and regional differentiation 2001 ·Human Immunology ·Kirsi Huoponen,Theodore G. Schurr,Yusheng Chen,Douglas C. Wallace	38
12	mtDNA Variation in the South African Kung and Khwe—and Their Genetic Relationships to Other African Populations 2000 ·The American Journal of Human Genetics ·Yusheng Chen,Antonel Olckers,Theodore G. Schurr,Andreas M. Kogelnik,Kirsi Huoponen,Douglas C. Wallace	151
13	Identification of SLC7A7, encoding y+LAT-1, as the lysinuric protein intolerance gene 1999 ·Nature Genetics ·David Torrents,Juha Mykkänen,Marta Pineda,Lídia Feliubadaló,Raúl Estévez,Rafael de Cid,Pablo Sanjurjo,António Zorzano,Virginia Nunes,Kirsi Huoponen,Arja Reinikainen,Olli Simell,Marja‐Liisa Savontaus,Pertti Aula,Manuel Palacı́n	232
14	Ophthalmologic Findings in Leber Hereditary Optic Neuropathy, with Special Reference to mtDNA Mutations 1996 ·Ophthalmology ·Eeva Nikoskelainen,Kirsi Huoponen,Vesa Juvonen,Tarja Lamminen,Kari Nummelin,(unknown)	150
15	A mitochondrial DNA (mtDNA) mutation associated with maternally inherited Parkinson`s disease (PD) and deafness 1994 ·The American Journal of Human Genetics ·John M. Shoffner,M S Brown,Kirsi Huoponen	2
16	Time-resolved fluorometry in the diagnosis of Leber hereditary optic neuroretinopathy 1994 ·Human Mutation ·Kirsi Huoponen,Vesa Juvonen,Antti Iitiä,Patrik Dahlén,Harri Siitari,Perttì Aula,Eeva Nikoskelainen,Marja‐Liisa Savontaus	10
17	Electron transfer properties of NADH: Ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON) 1991 ·FEBS Letters ·Anna Majander,Kirsi Huoponen,M L Savontaus,Eeva Nikoskelainen,Mårten Wikström	138
18	Recent advances in Leber's hereditary optic neuroretinopathy 1991 ·Eye ·Eeva Nikoskelainen,Johanna Vilkki,Kirsi Huoponen,Marja‐Liisa Savontaus	2
19	Analysis of mitochondrial ND4 gene DNA sequence in Finnish families with Leber hereditary optic neuroretinopathy 1990 ·Genomics ·Kirsi Huoponen,Johanna Vilkki,Marja‐Liisa Savontaus,Pertti Aula,(unknown)	10
20	Characterization of lignin peroxidase-encoding genes from lignin-degrading basidiomycetes 1990 ·Gene ·Kirsi Huoponen,Pauli Ollikka,M. Kälin,Isabelle Walther,Pekka Mäntsälä,Jakob Reiser	35

About Kirsi Huoponen

Kirsi Huoponen is a scholar working on Clinical Biochemistry, Biochemistry and Genetics, having authored 49 papers that have together received 3.4k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (20 papers), Metabolism and Genetic Disorders (16 papers) and Amino Acid Enzymes and Metabolism (11 papers). The work is most often cited by research in Clinical Biochemistry (938 citations), Biochemistry (298 citations) and Ophthalmology (329 citations). Kirsi Huoponen has collaborated with scholars based in Finland, United States and Italy. Frequent co-authors include Marja‐Liisa Savontaus, Eeva Nikoskelainen, Douglas C. Wallace, M L Savontaus, Tarja Lamminen, Antonio Torroni, Vesa Juvonen, Rosaria Scozzari, Paolo Francalacci and Laura Morelli. Their work appears in journals such as Nature Genetics, Genetics and Biochemical and Biophysical Research Communications.

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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