Minna Pöyhönen

6.6k citations

76 papers · 3.7k indexed · 1 hit paper · h-index 31

Neurology top 0.2%
- Cerebrovascular and genetic disorders 23
- Neurofibromatosis and Schwannoma Cases 23
- Neurological diseases and metabolism 7
- Neuroblastoma Research and Treatments 6
Neurology top 2%
- Cerebrovascular and genetic disorders 23
- Neurofibromatosis and Schwannoma Cases 23
- Neurological diseases and metabolism 7
- Neuroblastoma Research and Treatments 6
Rheumatology top 1%
- Moyamoya disease diagnosis and treatment 9
- Soft tissue tumor case studies 8
Immunology and Allergy top 2%
- Cell Adhesion Molecules Research 10
Pathology and Forensic Medicine top 5%
Renewable Energy, Sustainability and the Environment
- Metalloenzymes and iron-sulfur proteins 8

Co-authors: Hannu Kalimo Matti Viitanen Juha Peltonen Liisa Myllykangas Petra Pasanen Anders Paetau Sirkku Peltonen Maija Siitonen
Cited by: Neurology Rheumatology
Journals: Nature Medicine (2 papers)Journal of Clinical Oncology (2 papers)Brain (1 paper)
Partner nations: Finland Sweden United States

In The Last Decade

Minna Pöyhönen

73 papers receiving 3.6k citations

Hit Papers

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Peers

Countries citing papers authored by Minna Pöyhönen

Since Specialization

Citations

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

Fields of papers citing papers by Minna Pöyhönen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Minna Pöyhönen, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Minna Pöyhönen Line = papers co-authored together Minna Pöyhönen links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Craniofacial and dental features of Axenfeld‐Rieger syndrome patients with PITX2 mutations Orthodontics and Craniofacial Research ·Sirpa Arte,Minna Pöyhönen,Emmi Myllymäki,Elisa Ronkainen,David Rice,Pekka Nieminen	2023	4
2	Clinical features and spectrum of NOTCH3 variants in Finnish patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) Acta Neurologica Scandinavica ·Saana Mönkäre,Liina Kuuluvainen,Johanna Schleutker,Liisa Myllykangas,Minna Pöyhönen	2022	6
3	APOE ε4 associates with increased risk of severe COVID-19, cerebral microhaemorrhages and post-COVID mental fatigue: a Finnish biobank, autopsy and clinical study Acta Neuropathologica Communications ·Samu Kurki,Jonas Kantonen,Karri Kaivola,Laura Hokkanen,Mikko I. Mäyränpää,Henri Puttonen,(unknown),Juha Martola,Minna Pöyhönen,Mia Kero,Jarno Tuimala,Olli Carpén,Anu Kantele,Olli Vapalahti,Marjaana Tiainen,Pentti J. Tienari,Kai Kaila,Johanna Hästbacka,Liisa Myllykangas	2021	55
4	Constitutional mosaicism for a BRCA2 mutation as a cause of early-onset breast cancer Familial Cancer ·Pia Alhopuro,Reetta Vainionpää,Anna‐Kaisa Anttonen,Kristiina Aittomäki,Heli Nevanlinna,Minna Pöyhönen	2020	11
5	Identification of OAF and PVRL1 as candidate genes for an ocular anomaly characterized by Peters anomaly type 2 and ectopia lentis Experimental Eye Research ·D. David,Deepti Anand,Carlos Araújo,Brian Gloss,Joana Fino,Marcel E. Dinger,Päivi Lindahl,Minna Pöyhönen,Hannele Laivuori,João Lavinha	2018	5
6	Congenital anomalies in neurofibromatosis 1: a retrospective register-based total population study Orphanet Journal of Rare Diseases ·Jussi Leppävirta,Roope A. Kallionpää,Elina Uusitalo,Tero Vahlberg,Minna Pöyhönen,Juha Peltonen,Sirkku Peltonen	2018	21
7	Genetics of dementia in a Finnish cohort European Journal of Human Genetics ·Petra Pasanen,Liisa Myllykangas,Minna Pöyhönen,Anna Kiviharju,Maija Siitonen,John Hardy,José Brás,Anders Paetau,Pentti J. Tienari,Rita Guerreiro,Auli Verkkoniemi‐Ahola	2018	7
8	008 Congenital anomalies in neurofibromatosis 1: A retrospective register-based total population study Journal of Investigative Dermatology ·Jussi Leppävirta,Roope A. Kallionpää,E. Uusitalo,Minna Pöyhönen,Juha Peltonen,Sirkku Peltonen	2017	3
9	Prevalence of neurofibromatosis type 1 in the Finnish population Genetics in Medicine ·Roope A. Kallionpää,Elina Uusitalo,Jussi Leppävirta,Minna Pöyhönen,Sirkku Peltonen,Juha Peltonen	2017	105
10	SNCA mutation p.Ala53Glu is derived from a common founder in the Finnish population Neurobiology of Aging ·Petra Pasanen,Eino Palin,Risto Pohjolan-Pirhonen,Minna Pöyhönen,Juha O. Rinne,Markku Päivärinta,Mika H. Martikainen,Valtteri Kaasinen,Marja Hietala,Maria Gardberg,Anna Maija Saukkonen,Johanna Eerola‐Rautio,Seppo Kaakkola,Jukka Lyytinen,Pentti J. Tienari,Anders Paetau,Anu Suomalainen,Liisa Myllykangas	2016	8
11	Experimental studies of mitochondrial function in CADASIL vascular smooth muscle cells Experimental Cell Research ·Matti Viitanen,Erik Sundström,Marc Baumann,Minna Pöyhönen,Saara Tikka,Homira Behbahani	2012	25
12	Loss of SUFU Function in Familial Multiple Meningioma The American Journal of Human Genetics ·Mervi Aavikko,Song-Ping Li,Silva Saarinen,Pia Alhopuro,Eevi Kaasinen,Ekaterina Morgunova,Yilong Li,Kari Vesanen,Miriam J. Smith,D. Gareth Evans,Minna Pöyhönen,Anne Kiuru,Anssi Auvinen,Lauri A. Aaltonen,Jussi Taipale,Pia Vahteristo	2012	105
13	Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions Genetics in Medicine ·Pia E. Vuorela,Sirpa Ala‐Mello,Carola Saloranta,Maila Penttinen,Minna Pöyhönen,Kirsi Huoponen,Wiktor Borozdin,Birke Bausch,Elke Botzenhart,Christian Wilhelm,Helena Kääriäinen,Jürgen Kohlhase	2007	38
14	Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL Neurogenetics ·Johanna Annunen‐Rasila,Saara Finnilä,Kati Mykkänen,Jukka S. Moilanen,Johanna Veijola,Minna Pöyhönen,Matti Viitanen,Hannu Kalimo,Kari Majamaa	2006	14
15	Ophthalmologic Findings in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Ophthalmology ·Susanna Roine,Mika Harju,Tero Kivelä,Minna Pöyhönen,Eeva Nikoskelainen,Seppo Tuisku,Hannu Kalimo,Matti Viitanen,Paula Summanen	2006	30
16	Detection of the founder effect in Finnish CADASIL families European Journal of Human Genetics ·Kati Mykkänen,Marja‐Liisa Savontaus,Vesa Juvonen,Pertti Sistonen,Seppo Tuisku,Susanna Tuominen,Maila Penttinen,Johan Lundkvist,Matti Viitanen,Hannu Kalimo,Minna Pöyhönen	2004	43
17	Fibrosis and Stenosis of the Long Penetrating Cerebral Arteries: the Cause of the White Matter Pathology in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Brain Pathology ·Qing Miao,Timo Paloneva,Susanna Tuominen,Minna Pöyhönen,Seppo Tuisku,Matti Viitanen,Hannu Kalimo	2004	114
18	New Function for NF1 Tumor Suppressor Journal of Investigative Dermatology ·Jussi Koivunen,Heli Ylä‐Outinen,Timo Korkiamäki,Seija-Liisa Karvonen,Minna Pöyhönen,Matti Laato,Jaakko Karvonen,Sirkku Peltonen,Juha Peltonen	2000	29
19	Occult Neurofibroma and Increased S100 Protein in the Skin of Patients With Neurofibromatosis Type 1 Archives of Dermatology ·Seija-Liisa Karvonen,Matti Kallioinen,Heli Ylä‐Outinen,Minna Pöyhönen,Aarne Oikarinen,Juha Peltonen	2000	22
20	A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1 Nature Medicine ·Richard Crook,Auli Verkkoniemi,Jordi Pérez‐Tur,Nitin D. Mehta,Matt Baker,Henry Houlden,Matthew J. Farrer,Mike Hutton,Sarah Lincoln,John Hardy,Katrina Gwinn,Mirja Somer,Anders Paetau,Hannu Kalimo,Raija Ylikoski,Minna Pöyhönen,Steve Kucera,Matti Haltia	1998	265

About Minna Pöyhönen

Minna Pöyhönen is a scholar working on Neurology, Immunology and Allergy and Rheumatology, having authored 76 papers that have together received 3.7k indexed citations. Recurring topics across this work include Cerebrovascular and genetic disorders (23 papers), Neurofibromatosis and Schwannoma Cases (23 papers), Cell Adhesion Molecules Research (10 papers), Moyamoya disease diagnosis and treatment (9 papers), Soft tissue tumor case studies (8 papers), Metalloenzymes and iron-sulfur proteins (8 papers), Neurological diseases and metabolism (7 papers) and Neuroblastoma Research and Treatments (6 papers). The work is most often cited by research in Neurology (2.3k citations), Neurology (445 citations) and Rheumatology (783 citations). Minna Pöyhönen has collaborated with scholars based in Finland, Sweden and United States. Frequent co-authors include Hannu Kalimo, Matti Viitanen, Juha Peltonen, Liisa Myllykangas, Petra Pasanen, Anders Paetau, Sirkku Peltonen, Maija Siitonen, Roope A. Kallionpää and Elina Uusitalo. Their work appears in journals such as Nature Medicine, Journal of Clinical Oncology and Brain.

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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