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Germline Mutation of RPS20 , Encoding a Ribosomal Protein, Causes Predisposition to Hereditary Nonpolyposis Colorectal Carcinoma Without DNA Mismatch Repair Deficiency

Gastroenterology (New York, N.Y. 1943), 2014-09, Vol.147 (3), p.595-598.e5

2014

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Desmoid tumor patients carry an elevated risk of familial adenomatous polyposis

Journal of surgical oncology, 2016-02, Vol.113 (2), p.209-212

2016

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Promoter-specific alterations of APC are a rare cause for mutation-negative familial adenomatous polyposis

Genes chromosomes & cancer, 2014-10, Vol.53 (10), p.857-864

2014

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Methyltransferase expression and tumor suppressor gene methylation in sporadic and familial colorectal cancer

Genes chromosomes & cancer, 2015-12, Vol.54 (12), p.776-787

2015

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Molecular Analysis of Endometrial Tumorigenesis: Importance of Complex Hyperplasia Regardless of Atypia

Clinical cancer research, 2009-09, Vol.15 (18), p.5772-5783

2009

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A novel essential splice site variant in SPTB in a large hereditary spherocytosis family

Molecular genetics & genomic medicine, 2021-05, Vol.9 (5), p.e1641-n/a

2021

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Updates in the field of hereditary nonpolyposis colorectal cancer

Expert review of gastroenterology & hepatology, 2020-08, Vol.14 (8), p.707-720

2020

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CHEK2 Founder Variants and Thyroid Cancer Risk

Thyroid (New York, N.Y.), 2024-04, Vol.34 (4), p.477

2024

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PDPR Gene Variants Predisposing to Papillary Thyroid Cancer

Thyroid (New York, N.Y.), 2024-05, Vol.34 (5), p.575

2024

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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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Identification of DHX40 as a candidate susceptibility gene for colorectal and hematological neoplasia

Leukemia, 2023-11, Vol.37 (11), p.2301-2305

2023

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Sequencing of Lynch syndrome tumors reveals the importance of epigenetic alterations

Oncotarget, 2017-12, Vol.8 (64), p.108020-108030

2017

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Pseudoexons provide a mechanism for allele-specific expression of APC in familial adenomatous polyposis

Oncotarget, 2016-10, Vol.7 (43), p.70685-70698

2016

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Distinct Genetic and Epigenetic Signatures of Colorectal Cancers According to Ethnic Origin

Cancer epidemiology, biomarkers & prevention, 2012, Vol.21 (1), p.202-211

2012

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BMPR1A Mutations in Hereditary Nonpolyposis Colorectal Cancer Without Mismatch Repair Deficiency

Gastroenterology (New York, N.Y. 1943), 2011-07, Vol.141 (1), p.e23-e26

2011

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Breast carcinoma and Lynch syndrome: molecular analysis of tumors arising in mutation carriers, non-carriers, and sporadic cases

Breast cancer research : BCR, 2012-06, Vol.14 (3), p.R90-R90, Article R90

2012

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Abstract 4156: Multiple rare germline variants in a thyroid cancer family

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13_Supplement), p.4156-4156

2019

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Arterial Blood Gas Tensions After Resuscitation From Out-of-Hospital Cardiac Arrest: Associations With Long-Term Neurologic Outcome

Critical care medicine, 2014-06, Vol.42 (6), p.1463-1470

2014

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Therapeutic hypothermia after out-of-hospital cardiac arrest in Finnish intensive care units: the FINNRESUSCI study

Intensive care medicine, 2013-05, Vol.39 (5), p.826-837

2013

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Urinary cell cycle arrest biomarkers and chitinase 3-like protein 1 (CHI3L1) to detect acute kidney injury in the critically ill: a post hoc laboratory analysis on the FINNAKI cohort

Critical care (London, England), 2020-04, Vol.24 (1), p.144-10, Article 144

2020

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Gastroenterology (New York, N.Y. 1943), 2015-01, Vol.148 (1), p.259

2015

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Gastroenterology (New York, N.Y. 1943), 2015, Vol.148 (1), p.259-259

2015

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Admission interleukin-6 is associated with post resuscitation organ dysfunction and predicts long-term neurological outcome after out-of-hospital ventricular fibrillation

Resuscitation, 2014-11, Vol.85 (11), p.1573-1579

2014

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Urine NGAL as a biomarker for septic AKI: a critical appraisal of clinical utility—data from the observational FINNAKI study

Annals of intensive care, 2020-04, Vol.10 (1), p.51-51, Article 51

2020

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Genetic variants in SERPINA4 and SERPINA5, but not BCL2 and SIK3 are associated with acute kidney injury in critically ill patients with septic shock

Critical care (London, England), 2017-03, Vol.21 (1), p.47-47, Article 47

2017

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Germline Mutation of RPS20 , Encoding a Ribosomal Protein, Causes Predisposition to Hereditary Nonpolyposis Colorectal Carcinoma Without DNA Mismatch Repair Deficiency

Desmoid tumor patients carry an elevated risk of familial adenomatous polyposis

Promoter-specific alterations of APC are a rare cause for mutation-negative familial adenomatous polyposis

Methyltransferase expression and tumor suppressor gene methylation in sporadic and familial colorectal cancer

Molecular Analysis of Endometrial Tumorigenesis: Importance of Complex Hyperplasia Regardless of Atypia

A novel essential splice site variant in SPTB in a large hereditary spherocytosis family

Updates in the field of hereditary nonpolyposis colorectal cancer

CHEK2 Founder Variants and Thyroid Cancer Risk

PDPR Gene Variants Predisposing to Papillary Thyroid Cancer

Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition

Identification of DHX40 as a candidate susceptibility gene for colorectal and hematological neoplasia

Sequencing of Lynch syndrome tumors reveals the importance of epigenetic alterations

Pseudoexons provide a mechanism for allele-specific expression of APC in familial adenomatous polyposis

Distinct Genetic and Epigenetic Signatures of Colorectal Cancers According to Ethnic Origin

BMPR1A Mutations in Hereditary Nonpolyposis Colorectal Cancer Without Mismatch Repair Deficiency

Breast carcinoma and Lynch syndrome: molecular analysis of tumors arising in mutation carriers, non-carriers, and sporadic cases

Abstract 4156: Multiple rare germline variants in a thyroid cancer family

Arterial Blood Gas Tensions After Resuscitation From Out-of-Hospital Cardiac Arrest: Associations With Long-Term Neurologic Outcome

Therapeutic hypothermia after out-of-hospital cardiac arrest in Finnish intensive care units: the FINNRESUSCI study

Urinary cell cycle arrest biomarkers and chitinase 3-like protein 1 (CHI3L1) to detect acute kidney injury in the critically ill: a post hoc laboratory analysis on the FINNAKI cohort

Reply

Reply

Admission interleukin-6 is associated with post resuscitation organ dysfunction and predicts long-term neurological outcome after out-of-hospital ventricular fibrillation

Urine NGAL as a biomarker for septic AKI: a critical appraisal of clinical utility—data from the observational FINNAKI study

Genetic variants in SERPINA4 and SERPINA5, but not BCL2 and SIK3 are associated with acute kidney injury in critically ill patients with septic shock

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