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Long-term survival among colorectal cancer patients in Finland, 1991-2015: a nationwide population-based registry study

BMC cancer, 2022-04, Vol.22 (1), p.356-356, Article 356

2022

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Mono- and biallelic germline variants of DNA glycosylase genes in colon adenomatous polyposis families from two continents

Frontiers in oncology, 2022-10, Vol.12, p.870863-870863

2022

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Morbidity After Mechanical Bowel Preparation and Oral Antibiotics Prior to Rectal Resection: The MOBILE2 Randomized Clinical Trial

JAMA surgery, 2024-03

2024

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Accuracy of Finnish Cancer Registry colorectal cancer data: a comparison between registry data and clinical records

Scandinavian journal of gastroenterology, 2021-03, Vol.56 (3), p.247-251

2021

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Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition

Genetics in medicine, 2019-08, Vol.21 (8), p.1868-1873

2019

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Short- and Long-Term Survival among Elderly Colorectal Cancer Patients in Finland, 2006-2015: A Nationwide Population-Based Registry Study

Cancers, 2023-12, Vol.16 (1), p.135

2023

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Impact of Screening on Survival in Familial Adenomatous Polyposis

Journal of clinical gastroenterology, 2016-01, Vol.50 (1), p.40-44

2016

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Thyroid Carcinomas That Occur in Familial Adenomatous Polyposis Patients Recurrently Harbor Somatic Variants in APC , BRAF , and KTM2D

Thyroid (New York, N.Y.), 2020-03, Vol.30 (3), p.380-388

2020

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Preoperative oral antibiotics in colon surgery

The lancet. Gastroenterology & hepatology, 2020-09, Vol.5 (9), p.801-801

2020

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Preoperative oral antibiotics in colon surgery

The lancet. Gastroenterology & hepatology, 2020-09, Vol.5 (9), p.801-802

2020

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When should a drain be left in the abdominal cavity upon surgery?

Duodecim (Helsinki, Finland : 1961), 2017, Vol.133 (11), p.1063

2017

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Genetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathy

European heart journal, 2015-09, Vol.36 (34), p.2327-2337

2015

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Sleep-related breathing disorder in non-infectious pulmonary complications after pediatric allogeneic stem cell transplantation

Pediatric research, 2023-06, Vol.93 (7), p.1983-1989

2023

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Proteomics screening after pediatric allogenic hematopoietic stem cell transplantation reveals an association between increased expression of inhibitory receptor FCRL6 on γδ T cells and cytomegalovirus reactivation

Immunology and cell biology, 2024-07, Vol.102 (6), p.513-525

2024

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BK polyomavirus-associated hemorrhagic cystitis among pediatric allogeneic bone marrow transplant recipients: Treatment response and evidence for nosocomial transmission

Journal of clinical virology, 2013-01, Vol.56 (1), p.77-81

2013

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Respiratory viruses after paediatric allogenic haematopoietic stem cell transplantation

Infectious diseases (London, England), 2021-03, Vol.53 (3), p.214-217

2021

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Next-generation sequencing panels for hereditary hearing loss testing with approaches for difficult-to-sequence regions

Molecular genetics and metabolism, 2021-04, Vol.132, p.S221

2021

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eP345 - Next-generation sequencing panels for hereditary hearing loss testing with approaches for difficult-to-sequence regions

Molecular genetics and metabolism, 2021-04, Vol.132, p.S221-S221

2021

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MYH7 Genotype–Phenotype Correlation in a Cohort of Finnish Patients

Cardiogenetics, 2022-03, Vol.12 (1), p.122-132

2022

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Recessive TMOD1 mutation causes childhood cardiomyopathy

Communications biology, 2024-01, Vol.7 (1), p.7-7, Article 7

2024

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Intragenic polymorphisms of the vitamin D receptor gene associated with intervertebral disc degeneration

Spine (Philadelphia, Pa. 1976), 1998-12, Vol.23 (23), p.2477-2485

1998

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Clinical disease presentation and ECG characteristics of LMNA mutation carriers

Open heart, 2017-01, Vol.4 (1), p.e000474-e000474

2017

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1998 Volvo Award Winner in Basic Science Studies: Intragenic Polymorphisms of the Vitamin D Receptor Gene Associated With Intervertebral Disc Degeneration

Spine (Philadelphia, Pa. 1976), 1998-12, Vol.23 (23), p.2477-2485

1998

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Prevalence of RPGR-Mediated Retinal Dystrophy in an Unselected Cohort of Over 5000 Patients

Translational vision science & technology, 2022-01, Vol.11 (1), p.6-6

2022

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Genome-wide scan of obesity in Finnish sibpairs reveals linkage to chromosome Xq24

The journal of clinical endocrinology and metabolism, 2000-09, Vol.85 (9), p.3183-3190

2000

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Long-term survival among colorectal cancer patients in Finland, 1991-2015: a nationwide population-based registry study

Mono- and biallelic germline variants of DNA glycosylase genes in colon adenomatous polyposis families from two continents

Morbidity After Mechanical Bowel Preparation and Oral Antibiotics Prior to Rectal Resection: The MOBILE2 Randomized Clinical Trial

Accuracy of Finnish Cancer Registry colorectal cancer data: a comparison between registry data and clinical records

Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition

Short- and Long-Term Survival among Elderly Colorectal Cancer Patients in Finland, 2006-2015: A Nationwide Population-Based Registry Study

Impact of Screening on Survival in Familial Adenomatous Polyposis

Thyroid Carcinomas That Occur in Familial Adenomatous Polyposis Patients Recurrently Harbor Somatic Variants in APC , BRAF , and KTM2D

Preoperative oral antibiotics in colon surgery

Preoperative oral antibiotics in colon surgery

When should a drain be left in the abdominal cavity upon surgery?

Genetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathy

Sleep-related breathing disorder in non-infectious pulmonary complications after pediatric allogeneic stem cell transplantation

Proteomics screening after pediatric allogenic hematopoietic stem cell transplantation reveals an association between increased expression of inhibitory receptor FCRL6 on γδ T cells and cytomegalovirus reactivation

BK polyomavirus-associated hemorrhagic cystitis among pediatric allogeneic bone marrow transplant recipients: Treatment response and evidence for nosocomial transmission

Respiratory viruses after paediatric allogenic haematopoietic stem cell transplantation

Next-generation sequencing panels for hereditary hearing loss testing with approaches for difficult-to-sequence regions

eP345 - Next-generation sequencing panels for hereditary hearing loss testing with approaches for difficult-to-sequence regions

MYH7 Genotype–Phenotype Correlation in a Cohort of Finnish Patients

Recessive TMOD1 mutation causes childhood cardiomyopathy

Intragenic polymorphisms of the vitamin D receptor gene associated with intervertebral disc degeneration

Clinical disease presentation and ECG characteristics of LMNA mutation carriers

1998 Volvo Award Winner in Basic Science Studies: Intragenic Polymorphisms of the Vitamin D Receptor Gene Associated With Intervertebral Disc Degeneration

Prevalence of RPGR-Mediated Retinal Dystrophy in an Unselected Cohort of Over 5000 Patients

Genome-wide scan of obesity in Finnish sibpairs reveals linkage to chromosome Xq24

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