Editorial: Neuropathology of COVID-19

por Myllykangas, Liisa
Publicado 2023

Bayesian clustering and feature selection for cancer tissue samples

por Marttinen, Pekka, Myllykangas, Samuel, Corander, Jukka
Publicado 2009

Classification of human cancers based on DNA copy number amplification modeling

por Myllykangas, Samuel, Tikka, Jarkko, Böhling, Tom, Knuutila, Sakari, Hollmén, Jaakko
Publicado 2008

Targeted sequencing library preparation by genomic DNA circularization

por Myllykangas, Samuel, Natsoulis, Georges, Bell, John M, Ji, Hanlee P
Publicado 2011

Clinical features and spectrum of NOTCH3 variants in Finnish patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

por Mönkäre, Saana, Kuuluvainen, Liina, Schleutker, Johanna, Myllykangas, Liisa, Pöyhönen, Minna
Publicado 2022

Opinions on conscientious objection to induced abortion among Finnish medical and nursing students and professionals

por Nieminen, Petteri, Lappalainen, Saara, Ristimäki, Pauliina, Myllykangas, Markku, Mustonen, Anne-Mari
Publicado 2015

CanGEM: mining gene copy number changes in cancer

por Scheinin, Ilari, Myllykangas, Samuel, Borze, Ioana, Böhling, Tom, Knuutila, Sakari, Saharinen, Juha
Publicado 2008

Intracerebral Hemorrhage in the Oldest Old: A Population-Based Study (Vantaa 85+)

por Tanskanen, Maarit, Mäkelä, Mira, Myllykangas, Liisa, Rastas, Sari, Sulkava, Raimo, Paetau, Anders
Publicado 2012

Amygdala α-Synuclein Pathology in the Population-Based Vantaa 85+ Study

por Raunio, Anna, Myllykangas, Liisa, Kero, Mia, Polvikoski, Tuomo, Paetau, Anders, Oinas, Minna
Publicado 2017

Hippocampal Sclerosis in the Oldest Old: A Finnish Population-Based Study

por Kero, Mia, Raunio, Anna, Polvikoski, Tuomo, Tienari, Pentti J., Paetau, Anders, Myllykangas, Liisa
Publicado 2018

Comparative genomics and genome biology of invasive Campylobacter jejuni

por Skarp, C. P. A., Akinrinade, O., Nilsson, A. J. E., Ellström, P., Myllykangas, S., Rautelin, H.
Publicado 2015

High Expression of Complement Component 5 (C5) at Tumor Site Associates with Superior Survival in Ewing's Sarcoma Family of Tumour Patients

por Savola, Suvi, Klami, Arto, Myllykangas, Samuel, Manara, Cristina, Scotlandi, Katia, Picci, Piero, Knuutila, Sakari, Vakkila, Jukka
Publicado 2011

Obese people benefit from lumbar spinal stenosis surgery as much as people of normal weight

por Myllykangas, Henni, Ristolainen, Leena, Hurri, Heikki, Lohikoski, Jouni, Kautiainen, Hannu, Puisto, Ville, Österman, Heikki, Manninen, Mikko
Publicado 2021

Monogenic gene variants in lung transplant recipients with usual interstitial pneumonia

por Stark, Christoffer, Koskenvuo, Juha W., Nykänen, Antti, Seppälä, Eija H., Myllykangas, Samuel, Lemström, Karl, Raivio, Peter
Publicado 2022

Genetic analysis reveals novel variants for vascular cognitive impairment

por Mönkäre, Saana, Kuuluvainen, Liina, Schleutker, Johanna, Bras, Jose, Roine, Susanna, Pöyhönen, Minna, Guerreiro, Rita, Myllykangas, Liisa
Publicado 2022

The impact of oral appliance therapy with moderate mandibular advancement on obstructive sleep apnea and upper airway volume

por Pahkala, Riitta, Seppä, J., Myllykangas, R., Tervaniemi, J., Vartiainen, V. M., Suominen, A. L., Muraja-Murro, A.
Publicado 2019

Lewy-related pathology exhibits two anatomically and genetically distinct progression patterns: a population-based study of Finns aged 85+

por Raunio, Anna, Kaivola, Karri, Tuimala, Jarno, Kero, Mia, Oinas, Minna, Polvikoski, Tuomo, Paetau, Anders, Tienari, Pentti J., Myllykangas, Liisa
Publicado 2019

Anticoagulation Therapy After Biologic Aortic Valve Replacement

por Myllykangas, Monna E., Kiviniemi, Tuomas O., Gunn, Jarmo M., Salomaa, Veikko V., Pietilä, Arto, Niiranen, Teemu J., Aittokallio, Jenni
Publicado 2021

Case reports of two pedigrees with recessive arrhythmogenic right ventricular cardiomyopathy associated with homozygous Thr335Ala variant in DSG2

por Qadri, Sami, Anttonen, Olli, Viikilä, Juho, Seppälä, Eija H., Myllykangas, Samuel, Alastalo, Tero-Pekka, Holmström, Miia, Heliö, Tiina, Koskenvuo, Juha W.
Publicado 2017

A familial FTD associated with C9orf72 repeat expansion and dysplastic gangliocytoma

por Kero, Mia, Ferrari, Raffaele, Mok, Kin, Paetau, Anders, Tienari, Pentti J, Tynninen, Olli, Hardy, John, Momeni, Parastoo, Verkkoniemi-Ahola, Auli, Myllykangas, Liisa
Publicado 2013