Toll-like receptor genetic variants and colorectal cancer

Por Weber, Alexander NR, Försti, Asta
Publicado em 2014

Systematic enrichment analysis of gene expression profiling studies identifies consensus pathways implicated in colorectal cancer development

Por Lascorz, Jesús, Hemminki, Kari, Försti, Asta
Publicado em 2011

Single nucleotide polymorphisms (SNPs) are inherited from parents and they measure heritable events

Por Hemminki, Kari, Försti, Asta, Lorenzo Bermejo, Justo
Publicado em 2005

The ‘Common Disease-Common Variant’ Hypothesis and Familial Risks

Por Hemminki, Kari, Försti, Asta, Bermejo, Justo Lorenzo
Publicado em 2008

Consensus Pathways Implicated in Prognosis of Colorectal Cancer Identified Through Systematic Enrichment Analysis of Gene Expression Profiling Studies

Por Lascorz, Jesús, Chen, Bowang, Hemminki, Kari, Försti, Asta
Publicado em 2011

Origin of B-Cell Neoplasms in Autoimmune Disease

Por Hemminki, Kari, Liu, Xiangdong, Ji, Jianguang, Försti, Asta
Publicado no PLoS One (2016)

Do Reproductive Factors Influence T, N, and M Classes of Ductal and Lobular Breast Cancers? A Nation-Wide Follow-Up Study

Por Mousavi, Seyed Mohsen, Försti, Asta, Sundquist, Kristina, Hemminki, Kari
Publicado em 2013

Survival in Bladder and Renal Cell Cancers Is Familial

Por Ji, Jianguang, Försti, Asta, Sundquist, Jan, Lenner, Per, Hemminki, Kari
Publicado em 2008

Incidence and survival in non-hereditary amyloidosis in Sweden

Por Hemminki, Kari, Li, Xinjun, Försti, Asta, Sundquist, Jan, Sundquist, Kristina
Publicado em 2012

Incidence of hereditary amyloidosis and autoinflammatory diseases in Sweden: endemic and imported diseases

Por Hemminki, Kari, Li, Xinjun, Försti, Asta, Sundquist, Jan, Sundquist, Kristina
Publicado em 2013

Thalassemia and sickle cell anemia in Swedish immigrants: Genetic diseases have become global

Por Hemminki, Kari, Li, Xinjun, Försti, Asta, Sundquist, Jan, Sundquist, Kristina
Publicado no SAGE Open Med (2015)

Effect of autoimmune diseases on incidence and survival in subsequent multiple myeloma

Por Hemminki, Kari, Liu, Xiangdong, Försti, Asta, Ji, Jianguang, Sundquist, Jan, Sundquist, Kristina
Publicado em 2012

Subsequent brain tumors in patients with autoimmune disease

Por Hemminki, Kari, Liu, Xiangdong, Försti, Asta, Ji, Jianguang, Sundquist, Jan, Sundquist, Kristina
Publicado em 2013

Subsequent Type 2 Diabetes in Patients with Autoimmune Disease

Por Hemminki, Kari, Liu, Xiangdong, Försti, Asta, Sundquist, Jan, Sundquist, Kristina, Ji, Jianguang
Publicado no Sci Rep (2015)

Allelotyping of pooled DNA with 250 K SNP microarrays

Por Wilkening, Stefan, Chen, Bowang, Wirtenberger, Michael, Burwinkel, Barbara, Försti, Asta, Hemminki, Kari, Canzian, Federico
Publicado em 2007

The Incidence of Senile Cataract and Glaucoma is Increased in Patients with Plasma Cell Dyscrasias: Etiologic Implications

Por Hemminki, Kari, Försti, Asta, Tuuminen, Raimo, Hemminki, Otto, Goldschmidt, Hartmut, Sundquist, Kristina, Sundquist, Jan, Li, Xinjun
Publicado no Sci Rep (2016)

High-throughput genotyping of a common deletion polymorphism disrupting the TRY6 gene and its association with breast cancer risk

Por Wagner, Kerstin, Grzybowska, Ewa, Butkiewicz, Dorota, Pamula-Pilat, Jolanta, Pekala, Wioletta, Tecza, Karolina, Hemminki, Kari, Försti, Asta
Publicado em 2007

Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population

Por Marouf, Chaymaa, Göhler, Stella, Filho, Miguel Inacio Da Silva, Hajji, Omar, Hemminki, Kari, Nadifi, Sellama, Försti, Asta
Publicado no BMC Cancer (2016)

A review of the infection-associated cancers in North African countries

Por Hussein, Wafaa Mohamed, Anwar, Wagida A., Attaleb, Mohammed, Mazini, Loubna, Försti, Asta, Trimbitas, Roxana-Delia, Khyatti, Meriem
Publicado no Infect Agent Cancer (2016)

Pedigree based DNA sequencing pipeline for germline genomes of cancer families

Por Försti, Asta, Kumar, Abhishek, Paramasivam, Nagarajan, Schlesner, Matthias, Catalano, Calogerina, Dymerska, Dagmara, Lubinski, Jan, Eils, Roland, Hemminki, Kari
Publicado no Hered Cancer Clin Pract (2016)