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American Journal of Audiology|April 2, 2014
Higher prevalence of autoimmune diseases and longer spells of vertigo in patients affected with familial Ménière's disease: A clinical comparison of familial and sporadic Ménière's diseaseElina Hietikko, Martti Sorri, Minna Männikkö, et al.
European Journal of Medical Genetics|April 2, 2013
High incidence of Meniere-like symptoms in relatives of Meniere patients in the areas of Oulu University Hospital and Kainuu Central Hospital in FinlandElina Hietikko, Jouko Kotimäki, Martti Sorri, et al.
BMC Genetics|December 14, 2017
Functional polymorphisms in asporin and CILP together with joint loading predispose to hand osteoarthritisMari Taipale, Svetlana Solovieva, Päivi Leino-Arjas, et al.
Spine|December 21, 2016
A Whole Exome Study Identifies Novel Candidate Genes for Vertebral Bone Marrow Signal Changes (Modic Changes)Minna Kraatari, Sini Skarp, Jaakko Niinimäki, et al.
Acta Oto-Laryngologica|September 16, 2017
Concomitant diseases and their effect on disease prognosis in Meniere's disease: diabetes mellitus identified as a negative prognostic factorTeemu Pieskä, Jouko Kotimäki, Minna Männikkö, et al.
International Journal of Audiology|September 1, 2012
A replication study on proposed candidate genes in Ménière's disease, and a review of the current status of genetic studiesElina Hietikko, Jouko Kotimäki, Annaleena Okuloff, et al.
International Journal of Obesity (2005)|October 12, 2020
Maternal and infant prediction of the child BMI trajectories; studies across two generations of Northern Finland birth cohortsRozenn Nedelec, Jouko Miettunen, Minna Männikkö, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 25, 2011
Finnish familial Meniere disease is not linked to chromosome 12p12.3, and anticipation and cosegregation with migraine are not common findingsElina Hietikko, Jouko Kotimäki, Erna Kentala, et al.
Genes|June 24, 2022
New Genetic Variants in CYP2B6 and SLC6A Support the Role of Oxidative Stress in Familial Ménière's DiseaseSini Skarp, Johanna Korvala, Jouko Kotimäki, et al.
Annals of Human Genetics|May 21, 2019
Whole-exome sequencing suggests multiallelic inheritance for childhood-onset Ménière's diseaseSini Skarp, Laura Kanervo, Jouko Kotimäki, et al.
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