M. Verdijk

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Inheritance of mutations in the V 2 receptor gene in thirteen families with nephrogenic diabetes insipidus

A. Ouweland, N. Knoers, L. Monnens, 2015 .

Inheritance of mutations in the V2 receptor gene in thirteen families with nephrogenic diabetes insipidus.

B. V. van Oost, A. V. D. van den Ouweland, N. Knoers, 1994, Kidney international.

Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene.

B. V. van Oost, P. Deen, L. Monnens, 1994, American journal of human genetics.

Identification and characterization of a new gene in the human Xq28 region.

A. Poustka, F. Tamanini, B. V. van Oost, 1992, Human Molecular Genetics.

Presence of C11orf95–MKL2 fusion is a consistent finding in chondroid lipomas: a study of eight cases

B. Tops, B. Küsters, T. Mentzel, 2013, Histopathology.

The human AQP4 gene: definition of the locus encoding two water channel polypeptides in brain.

P. Agre, P. Deen, J. Jung, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Subcutaneous Angiomatoid Fibrous Histiocytoma Mimicking Metastatic Melanoma

W. Blokx, M. Verdijk, C. Wetzels, 2012, Case reports in pathology.

Insulin-like growth factors and insulin-like growth factor-binding proteins in relation to disease status and incidence of hypoglycaemia in patients with a gastrointestinal stromal tumour.

S. de Jong, P. Jager, B. Rikhof, 2009, Annals of oncology : official journal of the European Society for Medical Oncology.

EWSR1-ATF1 chimeric transcript in a myoepithelial tumor of soft tissue: a case report.

B. Tops, P. Slootweg, T. Mentzel, 2012, Human pathology.

Epithelioid Hemangioendothelioma: clinicopathologic, immunhistochemical, and molecular genetic analysis of 39 cases

J. V. van Gorp, T. Mentzel, A. Suurmeijer, 2014, Diagnostic Pathology.

Anatomy and Pathology / Oncology MultiModality Analysis Improves Survival Prediction in Enucleated Uveal Melanoma Patients

Harmen, Job van Riet, N. Naus, 2019 .

Assembly of carboxy-terminally deleted desmin in vimentin-free cells.

F. Ramaekers, J. Raats, H. Bloemendal, 1991, European journal of cell biology.

CDKN2A but not TP53 mutations nor HPV presence predict poor outcome in metastatic squamous cell carcinoma of the skin

W. Quint, W. Melchers, M. Ligtenberg, 2009, International journal of cancer.

Mutations in the vasopressin type 2 receptor gene (AVPR2) associated with nephrogenic diabetes insipidus

M. Rocchi, A. Ouweland, N. Knoers, 1992, Nature Genetics.

NR4A3 rearrangement reliably distinguishes between the clinicopathologically overlapping entities myoepithelial carcinoma of soft tissue and cellular extraskeletal myxoid chondrosarcoma

B. Tops, P. Slootweg, T. Mentzel, 2012, Virchows Archiv.

The human renin-binding protein gene (RENBP) maps in Xq28.

A. Poustka, B. V. van Oost, A. V. D. van den Ouweland, 1994, Genomics.

Nephrogenic diabetes insipidus: identification of the genetic defect

A. Ouweland, N. Knoers, J. Dreesen, 1993, Pediatric Nephrology.

INK4-ARF and p53 Mutations in Metastatic Cutaneous Squamous Cell Carcinoma: Case Report and Archival Study on the Use of Ink4a-ARF and p53 Mutation Analysis in Identification of the Corresponding Primary Tumor

P. D. de Wilde, D. Ruiter, M. Ligtenberg, 2005, The American journal of surgical pathology.

Requirement of human renal water channel aquaporin-2 for vasopressin-dependent concentration of urine.

B. V. van Oost, B. Wieringa, P. Deen, 1994, Science.

Clear Cell Odontogenic Carcinoma: Occurrence of EWSR1-CREB1 as Alternative Fusion Gene to EWSR1-ATF1

A. Eijkelenboom, E. Bloemena, M. Debiec‐Rychter, 2018, Head and Neck Pathology.

CDKN2A (INK4A-ARF) Mutation Analysis to Distinguish Cutaneous Melanoma Metastasis From a Second Primary Melanoma

M. Ligtenberg, W. Blokx, K. Punt, 2007, The American journal of surgical pathology.

Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutation

M. Ligtenberg, F. Waldhauser, A. F. V. Lieburg, 1995, Human Genetics.

Solitary fibrous tumor – clinicopathologic, immunohistochemical and molecular analysis of 28 cases

P. Slootweg, J. Bonenkamp, E. Ruijter, 2014, Diagnostic Pathology.

Soft tissue angiofibroma: Clinicopathologic, immunohistochemical and molecular analysis of 14 cases

P. Roepman, R. Vink, A. Flanagan, 2017, Genes, chromosomes & cancer.

Subcutaneous Angiomatoid Fibrous Histiocytoma

M. Verdijk, C. Wetzels, E. Sparreboom, 2017 .

Prognostic significance of NAB2–STAT6 fusion variants and TERT promotor mutations in solitary fibrous tumors/hemangiopericytomas of the CNS: not (yet) clear

P. Wesseling, D. Figarella-Branger, C. Bouvier, 2019, Acta Neuropathologica.

Mutual exclusion of t(11;18)(q21;q21) and numerical chromosomal aberrations in the development of different types of primary gastric lymphomas

A. Chott, M. Ligtenberg, M. Hoeve, 2003, British journal of haematology.

The QM gene is X-linked and therefore not involved in suppression of tumorigenesis in Wilms' tumor

A. Ouweland, M. Mannens, M. Verdijk, 1992, Human Genetics.