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Sorri, Martti
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1

New Genetic Variants in CYP2B6 and SLC6A Support the Role o..:

Skarp, Sini ; Korvala, Johanna ; Kotimäki, Jouko...
Genes.  13 (2022)  6 - p. 998 , 2022
Link: https://doi.org/10.3390/..
 
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2

Whole‐exome sequencing suggests multiallelic inheritance fo..:

Skarp, Sini ; Kanervo, Laura ; Kotimäki, Jouko...
Annals of Human Genetics.  83 (2019)  6 - p. 389-396 , 2019
Link: https://doi.org/10.1111/..
 
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3

A nonsynonymous mutation in the WFS1 gene in a Finnish fami..:

Kytövuori, Laura ; Hannula, Samuli ; Mäki-Torkko, Elina..
Hearing Research.  355 (2017)  - p. 97-101 , 2017
Link: https://doi.org/10.1016/..
 
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4

Hearing impairment is common among Saami adults in Northern..:

Lohi, Venla ; Ohtonen, Pasi ; Aikio, Pekka...
International Journal of Circumpolar Health.  76 (2017)  1 - p. 1398004 , 2017
Link: https://doi.org/10.1080/..
 
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5

Mutations in the two ribosomal RNA genes in mitochondrial D..:

Häkli, Sanna ; Luotonen, Mirja ; Sorri, Martti.
BMC Medical Genetics.  16 (2015)  1 - p. , 2015
Link: https://doi.org/10.1186/..
 
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6

Childhood hearing impairment in northern Finland, etiology ..:

Häkli, Sanna ; Luotonen, Mirja ; Bloigu, Risto..
International Journal of Pediatric Otorhinolaryngology.  78 (2014)  11 - p. 1852-1856 , 2014
Link: https://doi.org/10.1016/..
 
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7

High incidence of Meniere-like symptoms in relatives of Men..:

Hietikko, Elina ; Kotimäki, Jouko ; Sorri, Martti.
European Journal of Medical Genetics.  56 (2013)  6 - p. 279-285 , 2013
Link: https://doi.org/10.1016/..
 
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8

Finnish familial Meniere disease is not linked to chromosom..:

Hietikko, Elina ; Kotimäki, Jouko ; Kentala, Erna...
Genetics in Medicine.  13 (2011)  5 - p. 415-420 , 2011
Link: https://doi.org/10.1097/..
 
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9

Hearing Acuity as a Predictor of Walking Difficulties in Ol..:

Viljanen, Anne ; Kaprio, Jaakko ; Pyykkö, Ilmari...
Journal of the American Geriatrics Society.  57 (2009)  12 - p. 2282-2286 , 2009
Link: https://doi.org/10.1111/..
 
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10

GRM7 variants confer susceptibility to age-related hearing ..:

Friedman, Rick A. ; Van Laer, Lut ; Huentelman, Matthew J....
Human Molecular Genetics.  18 (2008)  4 - p. 785-796 , 2008
Link: https://doi.org/10.1093/..
 
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11

Counselling of hearing aid users is highly cost-effective:

Vuorialho, Arja ; Karinen, Petri ; Sorri, Martti
European Archives of Oto-Rhino-Laryngology.  263 (2006)  11 - p. 988-995 , 2006
Link: https://doi.org/10.1007/..
 
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12

Changes in hearing aid use over the past 20 years:

Vuorialho, Arja ; Sorri, Martti ; Nuojua, Irja.
European Archives of Oto-Rhino-Laryngology.  263 (2005)  4 - p. 355-360 , 2005
Link: https://doi.org/10.1007/..
 
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13

Hearing impairment in patients with 3243A→G mtDNA mutation:..:

Uimonen, Seija ; Moilanen, Jukka S. ; Sorri, Martti..
Human Genetics.  108 (2001)  4 - p. 284-289 , 2001
Link: https://doi.org/10.1007/..
 
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14

Prevalence of meniere disease in finland:

Kotimäki, Jouko ; Sorri, Martti ; Aantaa, Eero.
The Laryngoscope.  109 (1999)  5 - p. 748-753 , 1999
Link: https://doi.org/10.1097/..
 
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15

Expression of CYP2A genes in human liver and extrahepatic t..:

Koskela, Satu ; Hakkola, Jukka ; Hukkanen, Janne...
Biochemical Pharmacology.  57 (1999)  12 - p. 1407-1413 , 1999
Link: https://doi.org/10.1016/..
 
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