H. Havanka

A susceptibility locus for migraine with aura, on chromosome 4q24.

Jeanette C Papp, Leena Peltonen, Aarno Palotie, 2002, American journal of human genetics.

Testing of Variants of the MTHFR and ESR1 Genes in 1798 Finnish Individuals Fails to Confirm the Association with Migraine with Aura

J. Terwilliger, J. Kaprio, A. Palotie, 2006, Cephalalgia : an international journal of headache.

Familial migraine with and without aura: clinical characteristics and co‐occurrence

A. Palotie, M. Wessman, M. Kallela, 2001, European journal of neurology.

Tolfenamic Acid Rapid Release Versus Sumatriptan in the Acute Treatment of Migraine: Comparable Effect in a Double‐Blind, Randomized, Controlled, Parallel‐Group Study

V. Myllylä, H. Vapaatalo, H. Havanka, 1998, Headache.

Comorbidity in Finnish migraine families

A. Palotie, M. Wessman, M. Kallela, 2006, The Journal of Headache and Pain.

Modified‐Release Formulation of Tizanidine in Chronic Tension‐type Headache

H. Havanka, J. Peltola, K. Murros, 2000, Headache.

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

D. Strachan, M. Daly, A. Auton, 2018, Neuron.

Common Variant Burden C ontributes to the Familial Aggregation of Migraine in 1 , 589 Families Highlights

M. Daly, V. Salomaa, B. Neale, 2018 .

Common variant burden contributes significantly to the familial aggregation of migraine in 1,589 families

M. Daly, V. Salomaa, B. Neale, 2017, bioRxiv.

The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families

A. Palotie, M. Wessman, M. Kallela, 2018, Cephalalgia : an international journal of headache.

Efficacy of naratriptan tablets in the acute treatment of migraine: a dose-ranging study. Naratriptan S2WB2004 Study Group.

H. Diener, C. Dahlöf, H. Havanka, 2000, Clinical therapeutics.

Trait components provide tools to dissect the genetic susceptibility of migraine.

L. Peltonen, J. Terwilliger, E. Sobel, 2006, American journal of human genetics.

Chromosome 19p13 loci in Finnish migraine with aura families

Aarno Palotie, Jaakko Kaprio, Hanna Harno, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Neuropathology and Cardiovascular Regulation

J. Korpelainen, U. Tolonen, H. Havanka, 2000 .

Erratum: Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families (Neuron (2018) 98(4) (743–753.e4), (S0896627318303222) (10.1016/j.neuron.2018.04.014))

D. Strachan, M. Daly, A. Auton, 2018 .