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dr. P.G.J. (Peter) Nikkels

Assistant Professor - medical

  • Department of Pathology

dr. P.G.J. (Peter) Nikkels

Research Programs

Biography

Pathologist, consultant for pediatric and perinatal pathology.

MD exam July 1982, Erasmus Uni­versity Rotter­dam, the Netherlands

PhD thesis: The hemopoietic micro-environment, effects of chemotherapy and irradiation, March 22 1989, Erasmus Uni­versity Rotter­dam, the Netherlands

Pathology training: January 1987 until January 1992, University Hospital Groningen, the Netherlands

1992-december 1996: staff member department of pathology University Hospital Groningen, the Netherlands and responsible for the perinatal pathology

December 1996- : staff member department of pathology, University Hospital Utrecht, the Netherlands. Responsible for pediatric and perinatal pathology including training of residents and performing / supervising 120-140 perinatal and pediatric autopsies annually, 700-800 placentas annually and approximately 1200-1500 surgical biopsies including solid pediatric tumors from October 2014.

Research Output (277)

Prophylaxis of implant-related infections by local release of vancomycin from a hydrogel in rabbits

Boot W, Vogely H C, Nikkels P G, Pouran B, van Rijen M H, Ekkelenkamp M B, Hänsch G M, Dhert W J, Gawlitta D 19 feb 2020, In: European Cells & Materials. 39 , p. 108-120 13 p.

Clinical outcomes in chronic intervillositis of unknown etiology

Bos M., Harris-Mostert E. T.M.S., van der Meeren L. E., Baelde J. J., Williams D. J., Nikkels P. G.J., Bloemenkamp K. W.M., van der Hoorn M. L.P. 1 feb 2020, In: Placenta. 91 , p. 19-23 5 p.

Acardius anceps with neck cyst and cleft palate:Three dimensional skeletal computed tomography reconstruction with discussion of the literature

van Gemert Martin J.C., Streekstra Geert J., Vandenbussche Frank P.H.A., Nikkels Peter G.J., van den Wijngaard Jeroen P.H.M. 15 jan 2020, In: Birth Defects Research. 112 , p. 137-140 4 p.

Homozygous damaging SOD2 variant causes lethal neonatal dilated cardiomyopathy

Almomani Rowida, Herkert Johanna C., Posafalvi Anna, Post Jan G., Boven Ludolf G., Van Der Zwaag Paul A., Willems Peter H.G.M., Van Veen-Hof Ingrid H., Verhagen Judith M.A., Wessels Marja W., Nikkels Peter G.J., Wintjes Liesbeth T., Van Den Berg Maarten P., Sinke Richard J., Rodenburg Richard J., Niezen-Koning Klary E., Van Tintelen J. Peter, Jongbloed Jan D.H. 1 jan 2020, In: Journal of Medical Genetics. 57 , p. 23-30 8 p.

Biallelic variants in POLR3GL cause endosteal hyperostosis and oligodontia

Terhal Paulien A, Vlaar Judith M, Middelkamp Sjors, Nievelstein Rutger A J, Nikkels Peter G J, Ross Jamila, Créton Marijn, Bos Jeroen W, Voskuil-Kerkhof Elsbeth S M, Cuppen Edwin, Knoers Nine, van Gassen Koen L I jan 2020, In: European Journal of Human Genetics. 28 , p. 31-39 9 p.

TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental Abnormalities

Vandervore Laura V, Schot Rachel, Milanese Chiara, Smits Daphne J, Kasteleijn Esmee, Fry Andrew E, Pilz Daniela T, Brock Stefanie, Börklü-Yücel Esra, Post Marco, Bahi-Buisson Nadia, Sánchez-Soler María José, van Slegtenhorst Marjon, Keren Boris, Afenjar Alexandra, Coury Stephanie A, Tan Wen-Hann, Oegema Renske, de Vries Linda S, Fawcett Katherine A, Nikkels Peter G J, Bertoli-Avella Aida, Al Hashem Amal, Alwabel Abdulmalik A, Tlili-Graiess Kalthoum, Efthymiou Stephanie, Zafar Faisal, Rana Nuzhat, Bibi Farah, Houlden Henry, Maroofian Reza, Person Richard E, Crunk Amy, Savatt Juliann M, Turner Lisbeth, Doosti Mohammad, Karimiani Ehsan Ghayoor, Saadi Nebal Waill, Akhondian Javad, Lequin Maarten H, Kayserili Hülya, van der Spek Peter J, Jansen Anna C, Kros Johan M, Verdijk Robert M, Milošević Nataša Jovanov, Fornerod Maarten, Mastroberardino Pier Giorgio, Mancini Grazia M S 5 dec 2019, In: American Journal of Human Genetics. 105 , p. 1126-1147 22 p.

Ribosomal protein gene RPL9 variants can differentially impair ribosome function and cellular metabolism

Lezzerini Marco, Penzo Marianna, O'Donohue Marie-Françoise, Marques Dos Santos Vieira Carolina, Saby Manon, Elfrink Hyung L, Diets Illja J, Hesse Anne-Marie, Couté Yohann, Gastou Marc, Nin-Velez Alexandra, Nikkels Peter G J, Olson Alexandra N, Zonneveld-Huijssoon Evelien, Jongmans Marjolijn C J, Zhang GuangJun, van Weeghel Michel, Houtkooper Riekelt H, Wlodarski Marcin W, Kuiper Roland P, Bierings Marc B, van der Werff Ten Bosch Jutte, Leblanc Thierry, Montanaro Lorenzo, Dinman Jonathan D, Da Costa Lydie, Gleizes Pierre-Emmanuel, MacInnes Alyson W 4 dec 2019, In: Nucleic Acids Research. 48 , p. 770-787 18 p.

Biallelic Variants in ASNA1, Encoding a Cytosolic Targeting Factor of Tail-Anchored Proteins, Cause Rapidly Progressive Pediatric Cardiomyopathy

Verhagen Judith M.A., van den Born Myrthe, van der Linde Herma C., G J Nikkels Peter, Verdijk Rob M., Kivlen Maryann H., van Unen Leontine M.A., Baas Annette F., Ter Heide Henriette, van Osch-Gevers Lennie, Hoogeveen-Westerveld Marianne, Herkert Johanna C., Bertoli-Avella Aida M., van Slegtenhorst Marjon A., Wessels Marja W., Verheijen Frans W., Hassel David, Hofstra Robert M.W., Hegde Ramanujan S., van Hasselt Peter M., van Ham Tjakko J., van de Laar Ingrid M.B.H. 1 sep 2019, In: Circulation. Genomic and precision medicine. 12 , p. 397-406 10 p.

Hepatic symptoms and histology in 13 patients with a Zellweger spectrum disorder

Berendse Kevin, Koot Bart G.P., Klouwer Femke C.C., Engelen Marc, Roels Frank, Lacle Miangela M., Nikkels Peter G.J., Verheij Joanne, Poll-The Bwee Tien 1 sep 2019, In: Journal of Inherited Metabolic Disease. 42 , p. 955-965 11 p.

Symmetrical Thalamic Lesions in the Newborn:A Case Series

Pols T, de Vries L S, Salamon A Soltirovska, Nikkels P G J, Lichtenbelt K D, Mulder-de Tollenaer S M, Wezel-Meijler G van 26 mrt 2019, In: Neuropediatrics. 50 , p. 152-159 8 p.

All Research Output (277)