Heikki Rantala - Publications, H-index & Citations

Heikki Rantala

aalto university

36H指数

178论文数

4.0K被引数

收录论文 40

发表时间

Muscle biopsy and mitochondrial disease criteria as diagnostic tools for paediatric patients presenting with neuromuscular phenotypes: highlighting the role of secondary mitochondrial dysfunction

Neuromuscular Disorders

IF2.8

2026-02-06

OAAI

Milla-Riikka Hautakangas; Tommi Niskanen; Päivi Vieira; Heli Helander; Anne M. Portaankorva; Heikki Rantala; Reetta Hinttala; Johanna Uusimaa

PM-SAMPO: Semantic Portal for Heritage Object Provenance Research PM-SAMPO：文化遗产对象来源研究的语义门户

SEMANTIC WEB: ESWC 2025 SATELLITE EVENTS

IF0

2026-01-01

PREAI

Shoilee, Sarah Binta Alam; Ahola, Annastiina; Rantala, Heikki; Hyvonen, Eero; de Boer, Victor; van Ossenbruggen, Jacco; Legene, Susan

SampoSampo: A Portal for Studying Enriched Data and Semantic Connections on a Cultural Heritage Linked Open Data Cloud SampoSampo：一个用于研究文化遗产链接开放数据云中富集数据和语义连接的门户

SEMANTIC WEB: ESWC 2025 SATELLITE EVENTS

IF0

2026-01-01

PREAI

Hyvonen, Eero; Leskinen, Petri; Ahola, Annastiina; Rantala, Heikki; Tuominen, Jouni

Radiotherapy-induced vascular cognitive impairment 20 years after childhood brain tumor

NEURO-ONCOLOGY

IF13.4

2023-09-27

OAAI

Remes, Tiina Maria; Suo-Palosaari, Maria Helena; Arikoski, Pekka Matti; Harila, Marika; Koskenkorva, Paeivi Katri Tuulikki; Lahteenmaki, Paivi Maria; Lonnqvist, Tuula Riitta Irmeli; Ojaniemi, Marja Katariina; Pohjasniemi, Heli; Puosi, Riina; Ritari, Niina; Sirkia, Kirsti Helena; Sutela, Anna Kaarina; Toiviainen-Salo, Sanna-Maria; Rantala, Heikki Markku Johannes; Harila, Arja Helena

Recurrent febrile seizures and serum cytokines: a controlled follow-up study

PEDIATRIC RESEARCH

IF3.1

2022-09-23

OAAI

Hautala, Maria K.; Helander, Heli M.; Pokka, Tytti M-L; Koskela, Ulla, V; Rantala, Heikki M. J.; Uhari, Matti K.; Korkiamaki, Timo J.; Glumoff, Virpi; Mikkonen, Kirsi H.

Sampo-UI: A full stack JavaScript framework for developing semantic portal user interfaces Sampo-ui: 用于开发语义门户用户界面的全栈JavaScript框架

SEMANTIC WEB

IF2.9

2021-11-25

OAAI

Ikkala, Esko; Hyvonen, Eero; Rantala, Heikki; Koho, Mikko

Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and mitochondrial dysfunction DIAPH1的丢失导致SCBMS，联合免疫缺陷和线粒体功能障碍

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

IF11.2

2021-08-01

OAAI

Kaustio, Meri; Nayebzadeh, Naemeh; Hinttala, Reetta; Tapiainen, Terhi; Astrom, Pirjo; Mamia, Katariina; Pernaa, Nora; Lehtonen, Johanna; Glumoff, Virpi; Rahikkala, Elisa; Honkila, Minna; Olsen, Paivi; Hassinen, Antti; Polso, Minttu; Al Sukaiti, Nashat; Al Shekaili, Jalila; Al Kindi, Mahmood; Al Hashmi, Nadia; Almusa, Henrikki; Bulanova, Daria; Haapaniemi, Emma; Chen, Pu; Suo-Palosaari, Maria; Vieira, Paivi; Tuominen, Hannu; Kokkonen, Hannaleena; Al Macki, Nabil; Al Habsi, Huda; Lopponen, Tuija; Rantala, Heikki; Pietiainen, Vilja; Zhang, Shen-Ying; Renko, Marjo; Hautala, Timo; Al Farsi, Tariq; Uusimaa, Johanna; Saarela, Janna

Variants p.Q1236H and p.E1143G in mitochondrial DNA polymerase gamma POLG1 are not associated with increased risk for valproate-induced hepatotoxicity or pancreatic toxicity: A retrospective cohort study of patients with epilepsy

EPILEPSIA

IF6.6

2018-09-26

OAAI

Hynynen, Johanna; Pokka, Tytti; Komulainen-Ebrahim, Jonna; Myllynen, Paivi; Karppa, Mikko; Pylvanen, Laura; Kalviainen, Reetta; Sokka, Arja; Jyrkila, Aino; Lahdetie, Jaana; Haataja, Leena; Makitalo, Anna; Ylikotila, Pauli; Eriksson, Kai; Haapala, Piia; Ansakorpi, Hanna; Hinttala, Reetta; Vieira, Paivi; Majamaa, Kari; Rantala, Heikki; Uusimaa, Johanna

NHLRC2 variants identified in patients with fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA): characterisation of a novel cerebropulmonary disease

ACTA NEUROPATHOLOGICA

IF9.3

2018-02-08

OAAI

Uusimaa, Johanna; Kaarteenaho, Riitta; Paakkola, Teija; Tuominen, Hannu; Karjalainen, Minna K.; Nadaf, Javad; Varilo, Teppo; Uusi-Makela, Meri; Suo-Palosaari, Maria; Pietila, Ilkka; Hiltunen, Anniina E.; Ruddock, Lloyd; Alanen, Heli; Biterova, Ekaterina; Miinalainen, Ilkka; Salminen, Annamari; Soininen, Raija; Manninen, Aki; Sormunen, Raija; Kaakinen, Mika; Vuolteenaho, Reetta; Herva, Riitta; Vieira, Paivi; Dunder, Teija; Kokkonen, Hannaleena; Moilanen, Jukka S.; Rantala, Heikki; Nogee, Lawrence M.; Majewski, Jacek; Ramet, Mika; Hallman, Mikko; Hinttala, Reetta

Biallelic Variants in UBA5 Link Dysfunctional UFM1 Ubiquitin-like Modifier Pathway to Severe Infantile-Onset Encephalopathy UBA5中的双等位基因变体将功能失调的UFM1泛素样修饰因子途径与严重的婴儿型脑病联系起来

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2016-09-01

OAAI

Muona, Mikko; Ishimura, Ryosuke; Laari, Anni; Ichimura, Yoshinobu; Linnankivi, Tarja; Keski-Filppula, Riikka; Herva, Riitta; Rantala, Heikki; Paetau, Anders; Poyhonen, Minna; Obata, Miki; Uemura, Takefumi; Karhu, Thomas; Bizen, Norihisa; Takebayashi, Hirohide; McKee, Shane; Parker, Michael J.; Akawi, Nadia; McRae, Jeremy; Hurles, Matthew E.; Kuismin, Outi; Kurki, Mitja I.; Anttonen, Anna-Kaisa; Tanaka, Keiji; Palotie, Aarno; Waguri, Satoshi; Lehesjoki, Anna-Elina; Komatsu, Masaaki

Evaluating clinical mitochondrial respiratory chain enzymes from biopsy specimens presenting skewed probability distribution of activity data

Mitochondrion

IF4.5

2016-07-01

PREAI

Hautakangas, Milla-Riikka; Hinttala, Reetta; Rantala, Heikki; Nieminen, Pentti; Uusimaa, Johanna; Hassinen, Ilmo E.

Diurnal and Seasonal Occurrence of Febrile Seizures

PEDIATRIC NEUROLOGY

IF2.1

2015-04-01

PREAI

Mikkonen, Kirsi; Uhari, Matti; Pokka, Tytti; Rantala, Heikki

Biogenesis of the mitochondrial respiratory chain in children with severe multiorgan disorders

Mitochondrion

IF4.5

2012-09-01

PREAI

Hinttala, Reetta; Uusimaa, Johanna; Antonicka, Hana; Kokkonen, Hannaleena; Moilanen, Jukka S.; Rantala, Heikki; Majamaa, Kari; Shoubridge, Eric A.

Shared loci for migraine and epilepsy on chromosomes 14q12-q23 and 12q24.2-q24.3

NEUROLOGY

IF8.5

2012-01-17

OAAI

Polvi, A.; Siren, A.; Kallela, M.; Rantala, H.; Artto, V.; Sobel, E. M.; Palotie, A.; Lehesjoki, A. -E.; Wessman, M.

Analysis of functional consequences of haplogroup J polymorphisms m.4216T > C and m.3866T > C in human MT-ND1: Mutagenesis of homologous positions in Escherichia coli

Mitochondrion

IF4.5

2010-06-01

PREAI

Hinttala, Reetta; Kervinen, Marko; Uusimaa, Johanna; Maliniemi, Pilvi; Finnila, Saara; Rantala, Heikki; Remes, Anne M.; Hassinen, Ilmo E.; Majamaa, Kari

Preventive treatment for recurrent febrile seizures 复发性热性惊厥的预防性治疗

ANNALS OF MEDICINE

IF4.3

2009-07-08

OAAI

Rantala, H; Tarkka, R; Uhari, M

Practice-oriented evaluation of medical students during a pediatric course

MEDICAL TEACHER

IF4.4

2009-07-03

PREAI

Nuutinen, M; Vainionpaa, L; Kokkonen, J; Rantala, H; Tapanainen, P; Mottonen, M; Vayrynen, M; Uhari, M

Intermittent prednisolone and autoantibodies to GAD65 in juvenile neuronal ceroid lipofuscinosis

NEUROLOGY

IF8.5

2008-04-01

PREAI

Aberg, L.; Talling, M.; Harkonen, T.; Lonnqvist, T.; Knip, M.; Alen, R.; Rantala, H.; Tyynela, J.

Homozygous W748S mutation in the POLG1 gene in patients with juvenile-onset Alpers syndrome and status epilepticus

EPILEPSIA

IF6.6

2008-02-20

OAAI

Uusimaa, Johanna; Hinttala, Reetta; Rantala, Heikki; Paivarinta, Markku; Herva, Riitta; Roytta, Matias; Soini, Heidi; Moilanen, Jukka S.; Remes, Anne M.; Hassinen, Ilmo E.; Majamaa, Kari

Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children

ANNALS OF NEUROLOGY

IF7.7

2007-09-06

PREAI

Uusimaa, Johanna; Moilanen, Jukka S.; Vainionpaa, Leena; Tapanainen, Paivi; Lindholm, Paivi; Nuutinen, Matti; Lopponen, Tuija; Maki-Torkko, Elina; Rantala, Heikki; Majamaa, Kari

研究方向