Maria K Haanpää

7PUBLICATIONS
37CO-AUTHORS
Cardiovascular medicine and haematology not elsewhere classifiedNeurogeneticsMedical mycologyEducational technology and computingEpigenetics (incl. genome methylation and epigenomics)
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Publications (7)

|May 22, 2024
Comparison of the ABC and ACMG systems for variant classification.

Gunnar Houge, Eirik Bratland, Ingvild Aukrust

|Apr 12, 2022
Clinical and Genetic Characteristics of Finnish Patients with Autosomal Recessive and Dominant Non-Syndromic Hearing Loss Due to Pathogenic TMC1 Variants.

Minna Kraatari-Tiri, Maria K Haanpää, Tytti Willberg

|Aug 30, 2021
Report of a novel missense mutation in the MECP2 gene in a middle-aged man with intellectual disability syndrome.

Maria Arvio, Maria Haanpää, Pia Pohjola

|Apr 29, 2021
Thinking outside "The Box": Case-based didactics for medical education and the instructional legacy of Dr John M. Graham, Jr.

Pedro A Sanchez-Lara, Katheryn Grand, Maria K Haanpää

|Jun 09, 2019
High-Resolution Bisulfite-Sequencing of Peripheral Blood DNA Methylation in Early-Onset and Familial Risk Breast Cancer Patients.

Justin Chen, Maria K Haanpää, Joshua J Gruber

|Jan 25, 2019
ALG11-CDG syndrome: Expanding the phenotype.

Maria K Haanpää, Bobby G Ng, Natalie M Gallant

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Frequent Collaborators

1 joint publications

Maria Arvio

1 joint publications

Bobby G Ng

1 joint publications

Virginia Kimonis

1 joint publications

Eric A Muller