Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2
Houlden, H, Laura, M, Wavrant-De Vrièze, F, Blake, J, Wood, N, Reilly, M M
Published in Neurology (18.11.2008)
Published in Neurology (18.11.2008)
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A SIMPLE AND EFFICIENT SYNTHESIS OF 2-(N-PHENYLAMINO)- BENZOIC ACIDS
Chen, M. H., Beylin, V. G., Iakovleva, E., Kesten, S. J., Magano, J., Vrieze, D.
Published in Synthetic communications (01.01.2002)
Published in Synthetic communications (01.01.2002)
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Gut Instinct
DE VRIEZE, JOP
Published in Science (American Association for the Advancement of Science) (17.01.2014)
Published in Science (American Association for the Advancement of Science) (17.01.2014)
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The Promise of Poop
DE VRIEZE, JOP
Published in Science (American Association for the Advancement of Science) (30.08.2013)
Published in Science (American Association for the Advancement of Science) (30.08.2013)
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A full Genome Scan for Late Onset Alzheimer's Disease
Kehoe, Patrick, Vrieze, Fabienne Wavrant-De, Crook, Richard, Wu, William S., Holmans, Peter, Fenton, Iain, Spurlock, Gillian, Norton, Nadine, Williams, Hywel, Williams, Nigel, Lovestone, Simon, Perez-Tur, Jordi, Hutton, Mike, Chartier-Harlin, Marie-Christine, Shears, Shantia, Roehl, Kimberly, Booth, Jeremy, Van Voorst, Wendy, Ramic, Dzanan, Williams, Julie, Goate, Alison, Hardy, John, Owen, Michael J.
Published in Human molecular genetics (01.02.1999)
Published in Human molecular genetics (01.02.1999)
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Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals
Simon-Sanchez, Javier, Scholz, Sonja, Fung, Hon-Chung, Matarin, Mar, Hernandez, Dena, Gibbs, J. Raphael, Britton, Angela, de Vrieze, Fabienne Wavrant, Peckham, Elizabeth, Gwinn-Hardy, Katrina, Crawley, Anthony, Keen, Judith C., Nash, Josefina, Borgaonkar, Digamber, Hardy, John, Singleton, Andrew
Published in Human molecular genetics (01.01.2007)
Published in Human molecular genetics (01.01.2007)
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Pitfalls in the diagnosis and management of inguinal lymphogranuloma venereum: important lessons from a case series
Oud, Emerentiana Veronica, de Vrieze, Nynke Hesselina Neeltje, de Meij, Arjan, de Vries, Henry John C
Published in Sexually transmitted infections (01.06.2014)
Published in Sexually transmitted infections (01.06.2014)
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Candidate Gene Polymorphisms for Ischemic Stroke
Matarin, Mar, Brown, W Mark, Dena, Hernandez, Britton, Angela, De Vrieze, Fabienne Wavrant, Brott, Thomas G, Brown, Robert D, Worrall, Bradford B, Case, L Douglas, Chanock, Stephen J, Metter, E Jeffrey, Ferruci, Luigi, Gamble, Dale, Hardy, John A, Rich, Stephen S, Singleton, Andrew, Meschia, James F
Published in Stroke (1970) (01.11.2009)
Published in Stroke (1970) (01.11.2009)
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Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease
Hamshere, Marian L., Holmans, Peter A., Avramopoulos, Dimitrios, Bassett, Susan S., Blacker, Deborah, Bertram, Lars, Wiener, Howard, Rochberg, Nan, Tanzi, Rudolph E., Myers, Amanda, Wavrant-De Vrièze, Fabienne, Go, Rodney, Fallin, Daniele, Lovestone, Simon, Hardy, John, Goate, Alison, O'Donovan, Michael, Williams, Julie, Owen, Michael J.
Published in Human molecular genetics (15.11.2007)
Published in Human molecular genetics (15.11.2007)
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The tau H2 haplotype is almost exclusively Caucasian in origin
Evans, Whitney, Fung, Hon Chung, Steele, John, Eerola, Johanna, Tienari, Pentti, Pittman, Alan, Silva, Rohan de, Myers, Amanda, Vrieze, Fabienne Wavrant-De, Singleton, Andrew, Hardy, John
Published in Neuroscience letters (21.10.2004)
Published in Neuroscience letters (21.10.2004)
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Journal Article
National Protocol for Model-Based Selection for Proton Therapy in Head and Neck Cancer
Langendijk, Johannes A., Hoebers, Frank J.P., de Jong, Martin A., Doornaert, Patricia, Terhaard, Chris H.J., Steenbakkers, Roel J.H.M., Hamming-Vrieze, Olga, van de Kamer, Jeroen B., Verbakel, Wilko F.A.R., Keskin-Cambay, Fatma, Reitsma, Johannes B., van der Schaaf, Arjen, Boersma, Liesbeth J., Schuit, Ewoud
Published in International journal of particle therapy (01.06.2021)
Published in International journal of particle therapy (01.06.2021)
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Chromosome 21 BACE2 haplotype associates with Alzheimer's disease: A two-stage study
Myllykangas, Liisa, Wavrant-De Vrièze, Fabienne, Polvikoski, Tuomo, Notkola, Irma-Leena, Sulkava, Raimo, Niinistö, Leena, Edland, Steven D., Arepalli, Sampath, Adighibe, Omanma, Compton, Danielle, Hardy, John, Haltia, Matti, Tienari, Pentti J.
Published in Journal of the neurological sciences (15.09.2005)
Published in Journal of the neurological sciences (15.09.2005)
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Segmental uniparental isodisomy on 5q32-qter in a patient with childhood-onset schizophrenia
Seal, J L, Gornick, M C, Gogtay, N, Shaw, P, Greenstein, D K, Coffey, M, Gochman, P A, Stromberg, T, Chen, Z, Merriman, B, Nelson, S F, Brooks, J, Arepalli, S, Wavrant-De Vrièze, F, Hardy, J, Rapoport, J L, Addington, A M
Published in Journal of medical genetics (01.11.2006)
Published in Journal of medical genetics (01.11.2006)
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Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13?
Blom, Elin S., Holmans, Peter, Arepalli, Sampath, Adighibe, Omanma, Hamshere, Marian L., Gatz, Margaret, Pedersen, Nancy L., Bergem, A. L. Mina, Owen, Michael J., Hollingworth, Paul, Goate, Alison, Williams, Julie, Lannfelt, Lars, Hardy, John, Wavrant-De Vrièze, Fabienne, Glaser, Anna
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.09.2008)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.09.2008)
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IL1RN VNTR polymorphism in ischemic atroke : Analysis in 3 populations
WORRALL, Bradford B, BROTT, Thomas G, MESCHIA, James F, BROWN, Robert D, BROWN, W. Mark, RICH, Stephen S, AREPALLI, Sampath, WAVRANT-DE VRIEZE, Fabienne, DUCKWORTH, Jaime, SINGLETON, Andrew B, HARDY, John
Published in Stroke (1970) (2007)
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Published in Stroke (1970) (2007)
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