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Mari Auranen

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Finland

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Mari Auranen; Sari Kiuru-Enari; Mirja Somer; J Toppila; Emil Ylikallio; Henna Tyynismaa
Dominant GDAP1 founder mutation is a common cause of axonal Charcot-Marie-Tooth disease in Finland.
Olayinka Raheem; Tiina Suominen; Peter Hackman; Anna Vihola; Mari Auranen; Hannu Kalimo; Ibrahim Mahjneh; Mikko Kärppä; Hannu Haapasalo; Bjarne Udd
[Not Available].
Tero Ylisaukko-Oja; Maricela Alarcón; Rita M Cantor; Mari Auranen; Raija Vanhala; Elli Kempas; Lennart von Wendt; Irma Järvelä; Daniel Geschwind; Leena Peltonen
Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families.

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All Publications

2013: Mari Auranen; Sari Kiuru-Enari; Mirja Somer; J Toppila; Emil Ylikallio; Henna Tyynismaa
Dominant GDAP1 founder mutation is a common cause of axonal Charcot-Marie-Tooth disease in Finland.
Neurogenetics 2013;14(2):123-32.
2006: Olayinka Raheem; Tiina Suominen; Peter Hackman; Anna Vihola; Mari Auranen; Hannu Kalimo; Ibrahim Mahjneh; Mikko Kärppä; Hannu Haapasalo; Bjarne Udd
[Not Available].
Duodecim; lääketieteellinen aikakauskirja 2006;122(17):2130-6.
2006: Tero Ylisaukko-Oja; Maricela Alarcón; Rita M Cantor; Mari Auranen; Raija Vanhala; Elli Kempas; Lennart von Wendt; Irma Järvelä; Daniel Geschwind; Leena Peltonen
Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families.
Annals of neurology 2006;59(1):145-55.
2005: Tero Ylisaukko-Oja; Karola Rehnström; Mari Auranen; Raija Vanhala; Reija Alen; Elli Kempas; Pekka Ellonen; Joni A Turunen; Ismo Makkonen; Raili Riikonen; Taina Nieminen-von Wendt; Lennart von Wendt; Leena Peltonen; Irma Järvelä
Analysis of four neuroligin genes as candidates for autism.
European journal of human genetics : EJHG 2005;13(12):1285-92.
2005: Peter Hackman; Vesa Juvonen; Jaakko Sarparanta; Maila Penttinen; Tuula Aärimaa; M Uusitalo; Mari Auranen; Helena Pihko; R Alén; M Junes; Tuula Lönnqvist; Hannu Kalimo; Bjarne Udd
Enrichment of the R77C alpha-sarcoglycan gene mutation in Finnish LGMD2D patients.
Muscle & nerve 2005;31(2):199-204.
2003: Mari Auranen; Teppo Varilo; Reija Alen; Raija Vanhala; K Ayers; Elli Kempas; Tero Ylisaukko-Oja; Leena Peltonen; Irma Järvelä
Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland.
Molecular psychiatry 2003;8(10):879-84.
2002: Mari Auranen; Raija Vanhala; Teppo Varilo; Kristin Ayers; Elli Kempas; Tero Ylisaukko-Oja; Janet S Sinsheimer; Leena Peltonen; Irma Järvelä
A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27.
American journal of human genetics 2002;71(4):777-90.
2001: Mari Auranen; Sirpa Ala-Mello; Joni A Turunen; Irma Järvelä
Further evidence for linkage of autosomal-dominant medullary cystic kidney disease on chromosome 1q21.
Kidney international 2001;60(4):1225-32.
2001: Henna Haravuori; Anna Vihola; Volker Straub; Mari Auranen; Isabelle Richard; Sylvie Marchand; T Voit; Siegfried Labeit; Hannu Somer; Leena Peltonen; Jacques Beckmann; Bjarne Udd
Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate gene.
Neurology 2001;56(7):869-77.
2001: Mari Auranen; Raija Vanhala; M Vosman; M Levander; Teppo Varilo; M Hietala; Raili Riikonen; Leena Peltonen; Irma Järvelä
MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features.
Neurology 2001;56(5):611-7.
2000: Mari Auranen; T Nieminen; S Majuri; Raija Vanhala; Leena Peltonen; Irma Järvelä
Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families.
Molecular psychiatry 2000;5(3):320-2.
2000: Mari Auranen; Raija Vanhala; Irma Järvelä
[First gene connected to autism spectrum disorders has been found].
Duodecim; lääketieteellinen aikakauskirja 2000;116(20):2185-7.
2000: Mari Auranen; Juhani Rapola; Helena Pihko; Matti Haltia; Ilmo V V Leivo; Seppo Soinila; Ismo Virtanen; Hannu Kalimo; Louise V B Anderson; Pirkko Santavuori; Hannu Somer
Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain disease.
Neuromuscular disorders : NMD 2000;10(1):16-23.
1998: Pia Höglund; Mari Auranen; J Socha; K Popinska; H Nazer; U Rajaram; A Al Sanie; M Al-Ghanim; Christer Holmberg; Albert de La Chapelle; Juha Kere
Genetic background of congenital chloride diarrhea in high-incidence populations: Finland, Poland, and Saudi Arabia and Kuwait.
American journal of human genetics 1998;63(3):760-8.
1997: Hannu Somer; Mari Auranen
[Gene errors in muscular diseases].
Duodecim; lääketieteellinen aikakauskirja 1997;113(18):1795-802.