Marja Hietala

3.3k total citations
37 papers, 918 citations indexed

About

Marja Hietala is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Marja Hietala has authored 37 papers receiving a total of 918 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 11 papers in Genetics and 8 papers in Neurology. Recurrent topics in Marja Hietala's work include Mitochondrial Function and Pathology (5 papers), Genetic Neurodegenerative Diseases (5 papers) and Parkinson's Disease Mechanisms and Treatments (4 papers). Marja Hietala is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), Genetic Neurodegenerative Diseases (5 papers) and Parkinson's Disease Mechanisms and Treatments (4 papers). Marja Hietala collaborates with scholars based in Finland, Germany and Sweden. Marja Hietala's co-authors include Markku Päivärinta, Vesa Juvonen, Outi Vierimaa, Lauri A. Aaltonen, M.-L. Savontaus, Valtteri Kaasinen, Veli Kairisto, Maija Kiuru, Riitta Herva and Virpi Launonen and has published in prestigious journals such as Blood, Journal of Molecular Biology and Annals of Neurology.

In The Last Decade

Marja Hietala

37 papers receiving 895 citations

Peers

Countries citing papers authored by Marja Hietala

Since Specialization

Citations

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

Fields of papers citing papers by Marja Hietala

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marja Hietala

This figure shows the co-authorship network connecting the top 25 collaborators of Marja Hietala. A scholar is included among the top collaborators of Marja Hietala 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 Marja Hietala. Marja Hietala 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	Prenatal Coffin-Siris Syndrome: Expanding the Phenotypic and Genotypic Spectrum of the Disease 2023 ·Pediatric and Developmental Pathology ·(unknown), (unknown), Mirjami Mattila, Marja Hietala, Hannele Koillinen, Jukka Laine, Maria K. Haanpää	3
2	Hypomorphic mutations of TRIP11 cause odontochondrodysplasia 2019 ·JCI Insight ·(unknown), Tomasz M. Witkos, Sheila Unger, (unknown), John A. Follit, Johannes C. Hermann, Tim J. M. Welting, Virginia Fano, Marja Hietala, Nithiwat Vatanavicharn, Katharina Schoner, Jürgen W. Spranger, Miriam Schmidts, Bernhard Zabel, Gregory J. Pazour, Agnès Bloch‐Zupan, Gen Nishimura, Andrea Superti‐Furga, Martin Lowe, Ekkehart Lausch	61
3	TSC2 c.1864C>T variant associated with mild cases of tuberous sclerosis complex 2017 ·American Journal of Medical Genetics Part A ·Laura S. Farach, William T. Gibson, Steven Sparagana, Mark Nellist, Connie T. R. M. Stumpel, Marja Hietala, Elliott Friedman, Deborah A. Pearson, (unknown), (unknown), (unknown), Efrat Ben‐Shalom, Kit Sing Au, Hope Northrup	11
4	A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency 2017 ·eLife ·Baptiste Fouquet, Patrycja Pawlikowska, Sandrine Caburet, Céline J. Guigon, (unknown), Laura M. Tanner, Marja Hietala, Kaja Urbańska, (unknown), Bérangère Legois, Bettina Bessières, Alain Gougeon, Alexandra Benachi, Gabriel Livéra, Filippo Rosselli, Reiner A. Veitia, Micheline Misrahi	51
5	SNCA mutation p.Ala53Glu is derived from a common founder in the Finnish population 2016 ·Neurobiology of Aging ·Petra Pasanen, Eino Palin, (unknown), 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	8
6	[Parkinson's disease associated with a mutation in the PARK2 gene]. 2015 ·PubMed ·Valtteri Kaasinen, Marja Hietala, Mikko Kuoppamäki	1
7	Epidemiology of Huntington's disease in Finland 2014 ·Parkinsonism & Related Disorders ·Jussi Sipilä, Marja Hietala, Ari Siitonen, Markku Päivärinta, Kari Majamaa	31
8	PGAP2 Mutations, Affecting the GPI-Anchor-Synthesis Pathway, Cause Hyperphosphatasia with Mental Retardation Syndrome 2013 ·The American Journal of Human Genetics ·Peter Krawitz, Yoshiko Murakami, Angelika Rieß, Marja Hietala, Ulrike Krüger, Na Zhu, Taroh Kinoshita, Stefan Mundlos, Jochen Hecht, Peter N. Robinson, Denise Horn	85
9	Androgen receptor genotypes predict response to endocrine treatment in breast cancer patients 2011 ·British Journal of Cancer ·Kristina Lundin, (unknown), Marja Hietala, Christian Ingvar, Carsten Rose, Helena Jernström	30
10	Exploring the transcriptomic variation caused by the Finnish founder mutation of lysinuric protein intolerance (LPI) 2011 ·Molecular Genetics and Metabolism ·(unknown), (unknown), Laura M. Tanner, (unknown), Olli Nevalainen, Harri Niinikoski, Kirsti Näntö‐Salonen, Marja Hietala, Olli Simell, Juha Mykkänen	13
11	Array comparative genomic hybridization identifies a distinct DNA copy number profile in renal cell cancer associated with hereditary leiomyomatosis and renal cell cancer 2009 ·Genes Chromosomes and Cancer ·(unknown), Heli Lehtonen, Kowan Ja Jee, Shinsuke Ninomiya, Simon A. Joosse, Pia Vahteristo, Maija Kiuru, Auli Karhu, Heli Sammalkorpi, Sakari Vanharanta, Rainer Lehtonen, Henrik Edgren, Petra M. Nederlof, Marja Hietala, Kristiina Aittomäki, Riitta Herva, Sakari Knuutila, Lauri A. Aaltonen, Virpi Launonen	20
12	Genitopatellar syndrome in an adolescent female with severe osteoporosis and endocrine abnormalities 2009 ·American Journal of Medical Genetics Part A ·Maila Penttinen, Hannele Koillinen, Harri Niinikoski, Outi Mäkitie, Marja Hietala	14
13	What is ideal genetic counselling? A survey of current international guidelines 2008 ·European Journal of Human Genetics ·(unknown), Marja Hietala, Ulf Kristoffersson, Irmgard Nippert, Jörg Schmidtke, Jorge Sequeiros, Helena Kääriäinen	62
14	G.P.10.01 Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations 2007 ·Neuromuscular Disorders ·Ulrike Schara, (unknown), Marja Hietala, (unknown), (unknown), Carmelo Rodolico, Gudrun Schreiber, Haluk Topaloğlu, W Voss, Angela Abicht, Juliane Müller, Hanns Lochmüller	2
15	The occurrence of dominant spinocerebellar ataxias among 251 Finnish ataxia patients and the role of predisposing large normal alleles in a genetically isolated population 2005 ·Acta Neurologica Scandinavica ·Vesa Juvonen, Marja Hietala, Veli Kairisto, M.-L. Savontaus	54
16	Evidence of a founder effect for the RETGC1 (GUCY2D) 2943DelG mutation in Leber congenital amaurosis pedigrees of Finnish origin 2002 ·Human Mutation ·Sylvain Hanein, Isabelle Perrault, (unknown), Tuija Löppönen, Marja Hietala, S. Gerber, Marc Jeanpierre, Fabienne Barbet, Dominique Ducroq, (unknown), Arnold Munnich, Jean‐Michel Rozet, Josseline Kaplan	21
17	Familial Cutaneous Leiomyomatosis Is a Two-Hit Condition Associated with Renal Cell Cancer of Characteristic Histopathology 2001 ·American Journal Of Pathology ·Maija Kiuru, Virpi Launonen, Marja Hietala, Kristiina Aittomäki, Outi Vierimaa, Reijo Salovaara, Johanna Arola, Eero Pukkala, (unknown), Riitta Herva, Lauri A. Aaltonen	134
18	A retrospective study of long‐term psychosocial consequences and satisfaction after carrier testing in childhood in an autosomal recessive disease: aspartylglucosaminuria 2000 ·Clinical Genetics ·Otso Järvinen, Marja Hietala, (unknown), Maria Arvio, Antti Uutela, Perttì Aula, H Kääriäinen	20
19	Two novel mutations in a Canadian family with aspartylglucosaminuria and early outcome post bone marrow transplantation 1997 ·Clinical Genetics ·Arja Laitinen, Marja Hietala, James C. Haworth, Marlis L. Schroeder, L.E. Seargeant, Cheryl R. Greenberg, Perttì Aula	9
20	Identification of a novel mutation causing aspartylglucosaminuria reveals a mutation hotspot region in the aspartylglucosaminidase gene 1995 ·Human Mutation ·(unknown), Marja Hietala, Perttì Aula, Anu Jalanko, Leena Peltonen	24

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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