Jukka Pekka Mecklin


Ontology type: schema:Person     


Person Info

NAME

Jukka Pekka

SURNAME

Mecklin

Publications in SciGraph latest 50 shown

  • 2019-01 Appendiceal neoplasm risk associated with complicated acute appendicitis—a population based study in INTERNATIONAL JOURNAL OF COLORECTAL DISEASE
  • 2018-12 Contribution of allelic imbalance to colorectal cancer in NATURE COMMUNICATIONS
  • 2018-11-12 Recurrent groin hernia surgery after primary open inguinal procedures: a reappraisal of the open preperitoneal (Ugahary) technique in HERNIA
  • 2018-08 Molecular changes preceding endometrial and ovarian cancer: a study of consecutive endometrial specimens from Lynch syndrome surveillance in MODERN PATHOLOGY
  • 2018-04 High immune cell score predicts improved survival in pancreatic cancer in VIRCHOWS ARCHIV
  • 2017-12 Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2017-11 Uptake of genetic testing by the children of Lynch syndrome variant carriers across three generations in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-07 Endometrial cancer risk factors among Lynch syndrome women: a retrospective cohort study in BRITISH JOURNAL OF CANCER
  • 2015-12 DNA hypermethylation appears early and shows increased frequency with dysplasia in Lynch syndrome-associated colorectal adenomas and carcinomas in CLINICAL EPIGENETICS
  • 2015-09 3′-UTR poly(T/U) repeat of EWSR1 is altered in microsatellite unstable colorectal cancer with nearly perfect sensitivity in FAMILIAL CANCER
  • 2015-07 CTCF/cohesin-binding sites are frequently mutated in cancer in NATURE GENETICS
  • 2015-06 Combination of microsatellite instability and BRAF mutation status for subtyping colorectal cancer in BRITISH JOURNAL OF CANCER
  • 2015-02 Video-assisted surgery: suggestions for failure prevention in laparoscopic cholecystectomy in COGNITION, TECHNOLOGY & WORK
  • 2014-10 Identification of 33 candidate oncogenes by screening for base-specific mutations in BRITISH JOURNAL OF CANCER
  • 2013-12 A prospective randomized controlled multicenter trial comparing antibiotic therapy with appendectomy in the treatment of uncomplicated acute appendicitis (APPAC trial) in BMC SURGERY
  • 2013-12 Psychosocial consequences of predictive genetic testing for lynch syndrome and associations to surveillance behaviour in a 7-year follow-up study in FAMILIAL CANCER
  • 2013-11 BRAF mutation in sporadic colorectal cancer and Lynch syndrome in VIRCHOWS ARCHIV
  • 2013-06 Colorectal surveillance in Lynch syndrome families in FAMILIAL CANCER
  • 2012-11 Somatic MED12 mutations in uterine leiomyosarcoma and colorectal cancer in BRITISH JOURNAL OF CANCER
  • 2012-09 Uroepithelial and kidney carcinoma in Lynch syndrome in FAMILIAL CANCER
  • 2012-09 Causes of death of mutation carriers in Finnish Lynch syndrome families in FAMILIAL CANCER
  • 2012-07 Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk in NATURE GENETICS
  • 2012-06 Breast carcinoma and Lynch syndrome: molecular analysis of tumors arising in mutation carriers, non-carriers, and sporadic cases in BREAST CANCER RESEARCH
  • 2011-12 Systematic search for enhancer elements and somatic allelic imbalance at seven low-penetrance colorectal cancer predisposition loci in BMC MEDICAL GENETICS
  • 2011-03 Sharing genetic risk with next generation: mutation-positive parents’ communication with their offspring in Lynch Syndrome in FAMILIAL CANCER
  • 2010-12 Cancer occurrence during follow-up of the CAPP2 study -aspirin use for up to four years significantly reduces Lynch syndrome cancers for up to several years after completion of therapy in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2010-06 Recommendations to improve identification of hereditary and familial colorectal cancer in Europe in FAMILIAL CANCER
  • 2010 Surveillance in HEREDITARY COLORECTAL CANCER
  • 2009-08 The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling in NATURE GENETICS
  • 2008-08 ARLTS1 germline variants and the risk for breast, prostate, and colorectal cancer in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2007-04 No evidence for dual role of loss of heterozygosity in hereditary non-polyposis colorectal cancer in ONCOGENE
  • 2007-01 Serrated carcinomas form a subclass of colorectal cancer with distinct molecular basis in ONCOGENE
  • 2006-12 EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis in BMC CANCER
  • 2006-06 Compliance and Satisfaction with Long-Term Surveillance in Finnish HNPCC Families in FAMILIAL CANCER
  • 2005-12 Numbers of mutations to different types of colorectal cancer in BMC CANCER
  • 2005-09 Surveillance in Lynch Syndrome in FAMILIAL CANCER
  • 2005-06 Gene expression signatures for colorectal cancer microsatellite status and HNPCC in BRITISH JOURNAL OF CANCER
  • 2005-03 History of the International Collaborative Group on Hereditary NonPolyposis Colorectal Cancer in FAMILIAL CANCER
  • 2005-02 Comprehensive characterization of HNPCC-related colorectal cancers reveals striking molecular features in families with no germline mismatch repair gene mutations in ONCOGENE
  • 2003-04 Genome-wide allelotyping of 104 Finnish colorectal cancers reveals an excess of allelic imbalance in chromosome 20q in familial cases in ONCOGENE
  • 2003-03 History of the International Collaborative Group on Hereditary NonPolyposis Colorectal Cancer in FAMILIAL CANCER
  • 2002-10 The impact of upper GI endoscopy referral volume on the diagnosis of gastroesophageal reflux disease and its complications: a 1-year cross-sectional study in a referral area with 260,000 inhabitants in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2001-03 Genotype and phenotype in hereditary nonpolyposis colon cancer: a study of families with different vs. shared predisposing mutations in FAMILIAL CANCER
  • 1999-11 Chronic inflammation at the gastroesophageal junction (carditis) appears to be a specific finding related to Helicobacter pylori infection and gastroesophageal reflux disease in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 1999-04 Specialized columnar epithelium of the esophagogastric junction: prevalence and associations in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 1996-03 Biofeedback therapy in rectal prolapse patients in DISEASES OF THE COLON & RECTUM
  • 1995-11 Founding mutations and Alu-mediated recombination in hereditary colon cancer in NATURE MEDICINE
  • 1995-06 Frequency of hereditary nonpolyposis colorectal cancer in DISEASES OF THE COLON & RECTUM
  • 1994-12 Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer in NATURE GENETICS
  • 1993-10 Treatment and follow-up strategies in hereditary nonpolyposis colorectal carcinoma in DISEASES OF THE COLON & RECTUM
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