H. Görgens

M. Kloor, M. von Knebel Doeberitz, M. Loeffler, 2010, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

Microsatellite stable colorectal cancers in clinically suspected hereditary nonpolyposis colorectal cancer patients without vertical transmission of disease are unlikely to be caused by biallelic germline mutations in MYH.

H. Schackert, S. Krüger, H. Görgens, 2006, The Journal of molecular diagnostics : JMD.

Genetic alterations of the tumor suppressor gene PTEN/MMAC1 in human brain metastases.

G. Schackert, H. Schackert, S. Sobottka, 1999, Clinical cancer research : an official journal of the American Association for Cancer Research.

TLR4 and IL-18 gene variants in aggressive periodontitis.

A. Ziegler, H. Schackert, T. Hoffmann, 2008, Journal of clinical periodontology.

CARD15 gene variants in aggressive periodontitis.

H. Schackert, T. Hoffmann, H. Görgens, 2006, Journal of clinical periodontology.

Arg462Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer: a case-control study.

M. von Knebel Doeberitz, C. Engel, J. Rüschoff, 2005, The Lancet. Oncology.

Arg 462 Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer : a case-control study

C. Engel, J. Rüschoff, S. Krüger, 2022 .

Complete homozygous deletion of CTSC in an Iranian family with Papillon–Lefèvre syndrome

P. Hoffmann, H. Schackert, Stephanie Kannen, 2014, International journal of dermatology.

Functional Cathepsin C mutations cause different Papillon-Lefèvre syndrome phenotypes.

H. Schackert, P. Eickholz, T. Hoffmann, 2008, Journal of clinical periodontology.

Screening for large rearrangements of the BRCA1 gene in German breast or ovarian cancer families using semi‐quantitative multiplex PCR method

D. Horn, H. Schackert, S. Scherneck, 2003, Human mutation.

Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1

S. Boué, H. Schackert, R. Büttner, 2008, European Journal of Human Genetics.

Novel Mutations in the Cathepsin C Gene in Patients with Pre-pubertal Aggressive Periodontitis and Papillon-Lefèvre Syndrome

H. Schackert, P. Eickholz, T. Hoffmann, 2004, Journal of dental research.

Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

Aung Ko Win, M. von Knebel Doeberitz, B. Bonanni, 2021, European journal of cancer.

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Aung Ko Win, P. Møller, E. Hovig, 2019, Genetics in Medicine.

Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

Aung Ko Win, M. von Knebel Doeberitz, B. Bonanni, 2020, Genetics in Medicine.

Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Aung Ko Win, P. Møller, E. Hovig, 2020, Genetics in Medicine.

RET-protooncogene variants in patients with sporadic neoplasms of the digestive tract and the central nervous system

C. Pilarsky, R. Grützmann, G. Schackert, 2011, International Journal of Colorectal Disease.

Hemihyperplasia-multiple lipomatosis syndrome (HHML): a challenge in spinal care.

S. Tinschert, U. Liljenqvist, H. Görgens, 2008, Acta orthopaedica Belgica.

Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors

M. Nöthen, M. Kloor, T. Becker, 2012, Familial Cancer.

Association Between TAS2R38 Gene Polymorphisms and Colorectal Cancer Risk: A Case-Control Study in Two Independent Populations of Caucasian Origin

M. Kloor, K. Hemminki, A. Naccarati, 2011, PloS one.

TCF-3, 4 protein expression correlates with β-catenin expression in MSS and MSI-H colorectal cancer from HNPCC patients but not in sporadic colorectal cancers

H. Schackert, S. Krüger, P. Baláž, 2010, International Journal of Colorectal Disease.

Adenoma and colorectal cancer risks in Lynch syndrome, Lynch‐like syndrome and familial colorectal cancer type X

M. Kloor, M. von Knebel Doeberitz, M. Loeffler, 2021, International journal of cancer.

No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study

Aung Ko Win, M. von Knebel Doeberitz, B. Bonanni, 2021, Journal of clinical medicine.

Distribution of RET proto‐oncogene variants in children with appendicitis

M. Haase, A. Ziegler, H. Görgens, 2022, Molecular genetics & genomic medicine.

Identification of candidate predisposing copy number variants in familial and early‐onset colorectal cancer patients

A. V. van Kessel, R. Kuiper, H. Schackert, 2011, International journal of cancer.

Polymorphisms in CTNNBL1 in relation to colorectal cancer with evolutionary implications.

M. Kloor, C. Cruciat, M. Boutros, 2011, International journal of molecular epidemiology and genetics.

TLR4 and IL-18 Gene Variants in Chronic Periodontitis: Impact on Disease Susceptibility and Severity

H. Schackert, T. Hoffmann, H. Görgens, 2009, Immunological investigations.

Genomic rearrangements in MSH2, MLH1 or MSH6 are rare in HNPCC patients carrying point mutations.

C. Engel, H. Schackert, H. Saeger, 2007, Cancer letters.

Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR).

Dietmar Roesner, Andreas Ziegler, Inke R König, 2003, Human molecular genetics.

An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancer.

H. Schackert, H. Saeger, R. Koch, 1997, European journal of cancer.

Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study

M. Kloor, K. Hemminki, A. Naccarati, 2010, BMC gastroenterology.

Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study.

Katherine M. Tucker, Aung Ko Win, Swati G. Patel, 2021, The Lancet. Oncology.

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Aung Ko Win, P. Møller, E. Hovig, 2019, Genetics in Medicine.

Cathepsin C Gene Variants in Aggressive Periodontitis

A. Ziegler, T. Hoffmann, H. Görgens, 2008, Journal of dental research.

Mutational status of KIT and PDGFRA and expression of PDGFRA are not associated with prognosis after curative resection of primary gastrointestinal stromal tumors (GISTs)

H. Schackert, H. Saeger, G. Baretton, 2011, Journal of surgical oncology.

Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility.

Michael Krawczak, Henry Völzke, Barbara Burwinkel, 2010, Carcinogenesis.

Germline truncating-mutations in BRCA1 and MSH6 in a patient with early onset endometrial cancer

E. Schröck, D. Aust, T. Neuhann, 2012, BMC Cancer.

The Role of Ret Genomic Variants in Infantile Hypertrophic Pyloric Stenosis

H. Schackert, J. Genuneit, H. Görgens, 2011, European Journal of Pediatric Surgery.

Identification of six novel MSH2 and MLH1 germline mutations in HNPCC

D. Aust, H. Schackert, F. Theissig, 2003, Human mutation.

The additive effect of p53 Arg72Pro and RNASEL Arg462Gln genotypes on age of disease onset in Lynch syndrome patients with pathogenic germline mutations in MSH2 or MLH1.

M. von Knebel Doeberitz, C. Engel, H. Schackert, 2007, Cancer letters.

The additive effect of p 53 Arg 72 Pro and RNASEL Arg 462 Gln genotypes on age of disease onset in Lynch syndrome patients with pathogenic germline mutations in MSH 2 or MLH 1

C. Engel, H. Schackert, S. Krüger, 2007 .

Analysis of RET, ZEB2, EDN3 and GDNF Genomic Rearrangements in 80 Patients with Hirschsprung Disease (Using multiplex ligation‐dependent probe amplification)

A. Ziegler, H. Schackert, H. Görgens, 2009, Annals of human genetics.

Analysis of RET, ZEB2, EDN3 and GDNF Genomic Rearrangements in Central Congenital Hyperventilation Syndrome Patients by Multiplex Ligation‐dependent Probe Amplification

H. Schackert, H. Görgens, A. Serra, 2010, Annals of human genetics.