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Lista de obras de Mef Nilbert

A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome

artículo científico publicado en 2008

A parametric model for analyzing anticipation in genetically predisposed families

artículo científico publicado en 2009

A prognostic model for soft tissue sarcoma of the extremities and trunk wall based on size, vascular invasion, necrosis, and growth pattern

artículo científico publicado en 2010

A review of statistical methods for testing genetic anticipation: looking for an answer in Lynch syndrome

artículo científico publicado en 2010

A somatic BRCA2 mutation in RER+ endometrial carcinomas that specifically deletes the amino-terminal transactivation domain

artículo científico publicado en 1999

A specific translocation, t(12;14)(q14-15;q23-24), characterizes a subgroup of uterine leiomyomas

artículo científico publicado en 1988

Acta Oncologica and a new generation of scientists in oncology.

artículo científico publicado en 2014

Altered Expression of MLH1, MSH2, and MSH6 in Predisposition to Hereditary Nonpolyposis Colorectal Cancer

artículo científico publicado en 2003

An effect from anticipation also in hereditary nonpolyposis colorectal cancer families without identified mutations

artículo científico publicado en 2009

Association between preoperative plasma levels of tissue inhibitor of metalloproteinases 1 and rectal cancer patient survival

artículo científico publicado en 2004

BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish population.

artículo científico publicado en 2016

Balancing life with an increased risk of cancer: lived experiences in healthy individuals with Lynch syndrome

artículo científico publicado en 2014

Bayesian modeling for genetic anticipation in presence of mutational heterogeneity: a case study in Lynch syndrome

artículo científico publicado en 2011

Benefits from membership in cancer patient associations: relations to gender and involvement

artículo científico publicado en 2006

Benefits, barriers and opinions on multidisciplinary team meetings: a survey in Swedish cancer care.

artículo científico publicado en 2018

Beta-catenin activation through mutation is rare in rectal cancer

artículo científico publicado en 2001

Broad phenotypic spectrum in familial adenomatous polyposis; from early onset and severe phenotypes to late onset of attenuated polyposis with the first manifestation at age 72.

artículo científico publicado en 2008

CHEK2 1100delC in patients with metachronous cancers of the breast and the colorectum

artículo científico publicado en 2006

Cancer risks and immunohistochemical profiles linked to the Danish MLH1 Lynch syndrome founder mutation.

artículo científico publicado en 2012

Cancer survival rates on the rise in Denmark after 3-point plan. Quick investigation for suspected cancer disease is a foundation

artículo científico publicado en 2014

Captured voices in cancer: experiences from networking between individuals with experiential and professional knowledge

artículo científico publicado en 2007

Challenges in the identification of MSH6-associated colorectal cancer: rectal location, less typical histology, and a subset with retained mismatch repair function.

artículo científico publicado en 2011

Changing clinical presentation of angiosarcomas after breast cancer: from late tumors in edematous arms to earlier tumors on the thoracic wall.

artículo científico publicado en 2010

Characteristic chromosome abnormalities, including rearrangements of 6p, del(7q), +12, and t(12;14), in 44 uterine leiomyomas

scientific article published on 01 October 1990

Characteristic karyotypic anomalies identify subtypes of malignant fibrous histiocytoma

artículo científico publicado en 1989

Characterization of the 12q13-15 amplicon in soft tissue tumors

artículo científico publicado en 1995

Characterization of the CHOP breakpoints and fusion transcripts in myxoid liposarcomas with the 12;16 translocation

artículo científico publicado en 1994

Chemotherapy in Ewing's sarcoma. The Scandinavian Sarcoma Group experience

artículo científico publicado en 1999

Chromosome abnormalities in leiomyosarcomas

scientific article published on 01 September 1988

Chromosome rearrangements in two uterine sarcomas

scientific article published on 01 January 1990

Clinical trials information monologues transform to dialogues

artículo científico publicado en 2007

Clinicopathologic factors identify sporadic mismatch repair-defective colon cancers

artículo científico publicado en 2008

Complex karyotypic anomalies in a bizarre leiomyoma of the uterus

artículo científico publicado en 1989

Complex karyotypic changes, including rearrangements of 12q13 and 14q24, in two leiomyosarcomas

scientific article published on 01 September 1990

Cutaneous malignant melanoma show geographic and socioeconomic disparities in stage at diagnosis and excess mortality.

artículo científico publicado en 2016

Cytogenetic aberrations and heterogeneity of mutations in repeat-containing genes in a colon carcinoma from a patient with hereditary nonpolyposis colorectal cancer

scientific article published on 01 April 2002

Danish Lynch syndrome families

artículo científico publicado en 2008

Defective mismatch-repair as a minor tumorigenic pathway in Barrett esophagus-associated adenocarcinoma

artículo científico publicado en 2005

Defective mismatch-repair in patients with multiple primary tumours including colorectal cancer

artículo científico publicado en 2003

Deranged Wnt signaling is frequent in hereditary nonpolyposis colorectal cancer.

artículo científico publicado en 2011

Detection and precise mapping of germline rearrangements in BRCA1, BRCA2, MSH2, and MLH1 using zoom-in array comparative genomic hybridization (aCGH).

artículo científico publicado en 2008

Diagnostic and prognostic gene expression signatures in 177 soft tissue sarcomas: hypoxia-induced transcription profile signifies metastatic potential

artículo científico publicado en 2007

Different karyotypic abnormalities, t(1;6) and del(7), in two uterine leiomyomas from the same patient

artículo científico publicado en 1989

Differential expression of CK20, β-catenin, and MUC2/5AC/6 in Lynch syndrome and familial colorectal cancer type X

artículo científico publicado en 2017

Discovery-based protein expression profiling identifies distinct subgroups and pathways in leiomyosarcomas

scientific article published on 28 July 2014

Discrepancies between estimated and perceived risk of cancer among individuals with hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2007

Dissecting karyotypic patterns in colorectal tumors: two distinct but overlapping pathways in the adenoma-carcinoma transition.

artículo científico publicado en 2002

Distinct gene expression profiles in ovarian cancer linked to Lynch syndrome

artículo científico publicado en 2014

Distinct gene expression signatures in Lynch syndrome and familial colorectal cancer type X

article

Distinct gene expression signatures in lynch syndrome and familial colorectal cancer type x.

artículo científico publicado en 2013

Distinct sets of gene alterations in endometrial carcinoma implicate alternate modes of tumorigenesis

scientific article published on 01 May 2002

Efficient and reproducible identification of mismatch repair deficient colon cancer: validation of the MMR index and comparison with other predictive models

scientific article published on 17 December 2013

Evaluation of the tissue microarray technique for immunohistochemical analysis in rectal cancer

scientific article published on 01 June 2002

Ewing's sarcoma treatment in Scandinavia 1984-1990--ten-year results of the Scandinavian Sarcoma Group Protocol SSGIV

artículo científico publicado en 1998

Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing

artículo científico publicado en 2016

Experiences from tissue microarray in soft tissue sarcomas.

artículo científico publicado en 2004

Experiences from treatment-predictive KRAS testing; high mutation frequency in rectal cancers from females and concurrent mutations in the same tumor

artículo científico publicado en 2009

Expression defect size among unclassified MLH1 variants determines pathogenicity in Lynch syndrome diagnosis

artículo científico publicado en 2013

Expression profiling using tissue microarray in 211 malignant fibrous histiocytomas confirms the prognostic value of Ki-67

scientific article published on 07 August 2004

Ezrin expression in rectal cancer predicts time to development of local recurrence

artículo científico publicado en 2012

Ezrin expression predicts local recurrence and development of metastases in soft tissue sarcomas

scientific article published on 08 June 2011

Familial colorectal cancer type X: genetic profiles and phenotypic features.

artículo científico

Familial risk of tumors associated with hereditary non-polyposis colorectal cancer: a Swedish population-based study

artículo científico publicado en 2004

Family perspectives in lynch syndrome becoming a family at risk, patterns of communication and influence on relations.

artículo científico publicado en 2012

Fast-track access to urologic care for patients with macroscopic haematuria is efficient and cost-effective: results from a prospective intervention study. ⬇️

artículo científico publicado en 2016

Focus on the tumour periphery in MRI evaluation of soft tissue sarcoma: infiltrative growth signifies poor prognosis

artículo científico publicado en 2006

Frequent alterations of the PI3K/AKT/mTOR pathways in hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2010

Frequent mismatch-repair defects link prostate cancer to Lynch syndrome

artículo científico publicado en 2016

Function, information, and contributions: An evaluation of national multidisciplinary team meetings for rare cancers

artículo científico publicado en 2019

Functional characterization of MLH1 missense variants identified in Lynch syndrome patients.

artículo científico publicado en 2012

Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair protein

artículo científico publicado en 2014

Gain of chromosomal region 20q and loss of 18 discriminates between Lynch syndrome and familial colorectal cancer.

artículo científico publicado en 2012

Gene expression identifies heterogeneity of metastatic propensity in high-grade soft tissue sarcomas

artículo científico publicado en 2012

Gene expression profile of colon cancer cell lines treated with SN-38.

artículo científico publicado en 2010

Gene expression profiles relate to SS18/SSX fusion type in synovial sarcoma

artículo científico publicado en 2006

Genetic anticipation in Swedish Lynch syndrome families.

artículo científico publicado en 2017

Genetic profiles distinguish different types of hereditary ovarian cancer

artículo científico publicado en 2010

Genetic profiles of gastroesophageal cancer: combined analysis using expression array and tiling array--comparative genomic hybridization

artículo científico publicado en 2010

Genetic profiling differentiates second primary tumors from metastases in adult metachronous soft tissue sarcoma.

scientific article published on January 2008

Glioblastomas, astrocytomas and oligodendrogliomas linked to Lynch syndrome

artículo científico publicado en 2015

Hereditary colorectal cancer diagnostics: morphological features of familial colorectal cancer type X versus Lynch syndrome.

artículo científico publicado en 2012

Heterogenous mismatch-repair status in colorectal cancer

artículo científico publicado en 2014

High frequency of microsatellite instability and loss of mismatch-repair protein expression in patients with double primary tumors of the endometrium and colorectum

scientific article published on 01 May 2002

Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes

artículo científico publicado en 2008

Hypoxia-inducible factor 1α predicts recurrence in high-grade soft tissue sarcoma of extremities and trunk wall

artículo científico publicado en 2017

Identification of a Gene Located at Chromosome 5q21 that Is Mutated in Colorectal Cancers ⬇️

artículo científico publicado el 15 de marzo de 1991

Immunohistochemical patterns in rectal cancer: application of tissue microarray with prognostic correlations

artículo científico publicado en 2004

Immunoprofiles of colorectal cancer from Lynch syndrome

artículo científico publicado en 2018

Improved prognostication in soft tissue sarcoma: independent information from vascular invasion, necrosis, growth pattern, and immunostaining using whole-tumor sections and tissue microarrays

scientific article published on 01 September 2005

Inactivation of promoter 1B of APC causes partial gene silencing: evidence for a significant role of the promoter in regulation and causative of familial adenomatous polyposis.

artículo científico publicado en 2011

Increased risk of male cancer and identification of a potential prostate cancer cluster region in BRCA2.

artículo científico publicado en 2015

Independent origin of uterine leiomyomas with karyotypically identical alterations

artículo científico publicado en 1992

Indistinguishable genomic profiles and shared prognostic markers in undifferentiated pleomorphic sarcoma and leiomyosarcoma: different sides of a single coin?

artículo científico publicado en 2009

Interobserver variability in the evaluation of mismatch repair protein immunostaining.

artículo científico publicado en 2010

Intratumor versus intertumor heterogeneity in gene expression profiles of soft-tissue sarcomas

artículo científico publicado en 2005

Involvement of Chromatin Remodeling Genes and the Rho GTPases RhoB and CDC42 in Ovarian Clear Cell Carcinoma.

artículo científico publicado en 2017

Involvement of adenomatous polyposis coli (APC)/beta-catenin signalling in human breast cancer

scientific article published on 01 January 2000

Karyotypic rearrangements in 20 uterine leiomyomas

artículo científico publicado en 1988

Key roles for MYC, KIT and RET signaling in secondary angiosarcomas

artículo científico publicado en 2014

Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels

artículo científico publicado en 2009

Lack of activating c-SRC mutations at codon 531 in rectal cancer

artículo científico publicado en 2000

Lactase persistence and ovarian carcinoma risk in Finland, Poland and Sweden

artículo científico publicado en 2005

Limited impact on self-concept in individuals with Lynch syndrome; results from a national cohort study.

artículo científico publicado en 2011

Living with hereditary non-polyposis colorectal cancer; experiences from and impact of genetic testing

artículo científico publicado en 2007

Long-range PCR facilitates the identification of PMS2-specific mutations.

artículo científico publicado en 2006

Loss of mismatch repair protein immunostaining in colorectal adenomas from patients with hereditary nonpolyposis colorectal cancer

Low expression of CysLT1R and high expression of CysLT2R mediate good prognosis in colorectal cancer

artículo científico publicado en 2010

Low frequency of defective mismatch repair in a population-based series of upper urothelial carcinoma

artículo científico publicado en 2005

Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) Diagnostics

MDM2 gene amplification correlates with ring chromosome in soft tissue tumors

artículo científico publicado en 1994

Major contribution from recurrent alterations and MSH6 mutations in the Danish Lynch syndrome population.

artículo científico

Microsatellite instability analysis and/or immunostaining for the diagnosis of hereditary nonpolyposis colorectal cancer?

article

Microsatellite instability and expression of MLH1 and MSH2 in carcinomas of the small intestine

artículo científico publicado en 2003

Microsatellite instability is rare in rectal carcinomas and signifies hereditary cancer

scientific article published on 01 June 1999

Mismatch repair defective breast cancer in the hereditary nonpolyposis colorectal cancer syndrome.

artículo científico publicado en 2009

Molecular subtyping of serous ovarian tumors reveals multiple connections to intrinsic breast cancer subtypes

artículo científico publicado en 2014

Monoclonal origin of endometriotic cysts

artículo científico publicado en 1995

Multidisciplinary team conferences promote treatment according to guidelines in rectal cancer

artículo científico publicado en 2014

Mutation spectrum in South American Lynch syndrome families

scientific article published on 18 December 2013

No amplification or rearrangement of INT1, GLI, or COL2A1 in uterine leiomyomas with t(12;14)(q14-15;q23-24)

scientific article published on 01 June 1989

No evidence of increased breast cancer risk for proven noncarriers from BRCA1 and BRCA2 families.

artículo científico publicado en 2016

No rearrangements of the CHOP gene in malignant fibrous histiocytoma.

artículo científico publicado en 1994

Novel germline APC mutations in Swedish patients with familial adenomatous polyposis and Gardner syndrome

scientific article published on 01 November 2000

One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations: results of a prospective study in Southern Sweden

scientific article published on 01 February 2004

Ovarian cancer at young age. Response to letter of Escobar et al

artículo científico publicado en 2008

Ovarian cancer at young age: the contribution of mismatch-repair defects in a population-based series of epithelial ovarian cancer before age 40

artículo científico publicado en 2007

Ovarian cancer linked to Lynch syndrome typically presents as early-onset, non-serous epithelial tumors

artículo científico publicado en 2011

Patient representatives' views on patient information in clinical cancer trials

artículo científico publicado en 2016

Patients' involvement in improving cancer care: experiences in three years of collaboration between members of patient associations and health care professionals.

artículo científico publicado en 2006

Phenotypic heterogeneity in hereditary non-polyposis colorectal cancer: identical germline mutations associated with variable tumour morphology and immunohistochemical expression.

artículo científico publicado en 2006

Pigmented villonodular synovitis. Monoclonality and metastasis--a case for neoplastic origin?

scientific article published on 01 February 1995

Preoperative Plasma Soluble Urokinase Plasminogen Activator Receptor as a Prognostic Marker in Rectal Cancer Patients. An Eortc-Receptor and Biomarker Group Collaboration

scientific article published on 01 April 2005

Progesterone stimulates degradation of urokinase plasminogen activator (u-PA) in endometrial stromal cells by increasing its inhibitor and surface expression of the u-PA receptor ⬇️

artículo científico publicado el 1 de septiembre de 1995

Prognostic impact of array-based genomic profiles in esophageal squamous cell cancer

artículo científico publicado en 2008

Prognostic importance of the soluble plasminogen activator receptor, suPAR, in plasma from rectal cancer patients

artículo científico publicado en 2001

Prognostic value of cell adhesion in esophageal adenocarcinomas

artículo científico publicado en 2008

Prognostic value of proliferation in pleomorphic soft tissue sarcomas: a new look at an old measure.

artículo científico publicado en 2012

Renal cell cancer linked to Lynch syndrome: Increased incidence and loss of mismatch repair protein expression

artículo científico publicado en 2016

Ring formation and structural rearrangements of chromosome 1 as secondary changes in uterine leiomyomas with t(12;14)(q14-15;q23-24)

scientific article published on 01 December 1988

Risk of Synchronous and Metachronous Colorectal Cancer: Population-Based Estimates in Denmark with Focus on Non-Hereditary Cases Diagnosed After Age 50

artículo científico publicado en 2018

Role for genetic anticipation in Lynch syndrome

artículo científico publicado en 2008

Sarcomas associated with hereditary nonpolyposis colorectal cancer: broad anatomical and morphological spectrum

artículo científico publicado en 2009

Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCC.

artículo científico publicado en 2004

Sense of coherence and self-concept in Lynch syndrome

artículo científico publicado en 2013

Sex Steroid Hormone Receptor Expression Affects Ovarian Cancer Survival

artículo científico publicado en 2015

Simple guidelines for efficient referral of soft-tissue sarcomas: a population-based evaluation of adherence to guidelines and referral patterns.

artículo científico publicado en 2012

Small soft tissue sarcomas do metastasize: identification of high-risk tumors

artículo científico publicado en 2014

Socioeconomic inequalities in breast cancer incidence and mortality in Europe-a systematic review and meta-analysis.

scientific article published on 23 May 2016

Somatic frameshift alterations in mononucleotide repeat-containing genes in different tumor types from an HNPCC family with germline MSH2 mutation

scientific article published on 01 September 2000

Standardizing evaluation of sarcoma proliferation- higher Ki-67 expression in the tumor periphery than the center

scientific article published on 01 June 2007

Supporter or obstructer; experiences from contact person activities among Swedish women with breast cancer

artículo científico publicado en 2005

The 5' region of the MSH2 gene involved in hereditary non-polyposis colorectal cancer contains a high density of recombinogenic sequences

scientific article published on 01 September 2005

The added value of PMS2 immunostaining in the diagnosis of hereditary nonpolyposis colorectal cancer

The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer

scientific article published on 19 December 2005

The power of empirical data; lessons from the clinical registry initiatives in Scandinavian cancer care

scientific article published on 26 September 2020

The predictive value of KRAS, NRAS, BRAF, PIK3CA and PTEN for anti-EGFR treatment in metastatic colorectal cancer: A systematic review and meta-analysis

artículo científico publicado en 2014

Tissue microarray technique in soft tissue sarcoma: immunohistochemical Ki-67 expression in malignant fibrous histiocytoma.

artículo científico publicado en 2001

Towards optimised information about clinical trials; identification and validation of key issues in collaboration with cancer patient advocates ⬇️

artículo científico publicado el 26 de agosto de 2010

Transforming growth factor beta1 in the human endometrium. Cyclic variation, increased expression by estradiol and progesterone, and regulation of plasminogen activators and plasminogen activator inhibitor-1.

artículo científico publicado en 1998

Urinary Tract Cancer in Lynch Syndrome; Increased Risk in Carriers of MSH2 Mutations.

artículo científico publicado en 2015

Validation of a self-concept scale for Lynch syndrome in different nationalities.

artículo científico publicado en 2011

[Alarming increase in skin cancer. Doubled number of cases within 10 years, according to forecasts from southern Sweden]

scientific article published on 01 August 2014

[Essential to discover hereditary colorectal and endometrial cancer. Mutations in "HNPCC individuals" can cause several different tumors]

artículo científico publicado en 2002

hMLH1, hMSH2 and hMSH6 mutations in hereditary non-polyposis colorectal cancer families from southern Sweden

artículo científico publicado en 1999

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