Detection of people at risk of developing a first psychosis: comparison of two recruitment strategies
Rietdijk, J., Klaassen, R., Ising, H., Dragt, S., Nieman, D. H., van de Kamp, J., Cuijpers, P., Linszen, D., van der Gaag, M.
Published in Acta psychiatrica Scandinavica (01.07.2012)
Published in Acta psychiatrica Scandinavica (01.07.2012)
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Clinical features and X-inactivation in females heterozygous for creatine transporter defect
van de Kamp, JM, Mancini, GMS, Pouwels, PJW, Betsalel, OT, van Dooren, SJM, de Koning, I, Steenweg, ME, Jakobs, C, van der Knaap, MS, Salomons, GS
Published in Clinical genetics (01.03.2011)
Published in Clinical genetics (01.03.2011)
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The Diversity of Nitrogen-Cycling Microbial Genes in a Waste Stabilization Pond Reveals Changes over Space and Time that Is Uncoupled to Changing Nitrogen Chemistry
Rose, A., Padovan, A., Christian, K., van de Kamp, J., Kaestli, M., Tsoukalis, S., Bodrossy, L., Gibb, K.
Published in Microbial ecology (01.05.2021)
Published in Microbial ecology (01.05.2021)
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Journal Article
The etiological evaluation of sensorineural hearing loss in children
van Beeck Calkoen, E. A., Engel, M. S. D., van de Kamp, J. M., Yntema, H. G., Goverts, S.T., Mulder, M.F., Merkus, P., Hensen, E. F.
Published in European journal of pediatrics (01.08.2019)
Published in European journal of pediatrics (01.08.2019)
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Journal Article
Clinical and genetic spectrum of Sanfilippo type C (MPS IIIC) disease in The Netherlands
Ruijter, G.J.G., Valstar, M.J., van de Kamp, J.M., van der Helm, R.M., Durand, S., van Diggelen, O.P., Wevers, R.A., Poorthuis, B.J., Pshezhetsky, A.V., Wijburg, F.A.
Published in Molecular genetics and metabolism (01.02.2008)
Published in Molecular genetics and metabolism (01.02.2008)
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Equivalent currents associated with morning-sector geomagnetic Pc5 pulsations during auroral substorms
Kauristie, K., Uspensky, M. V., Kleimenova, N. G., Kozyreva, O. V., Van De Kamp, M. M. J. L., Dubyagin, S. V., Massetti, S.
Published in Annales geophysicae (1988) (07.04.2016)
Published in Annales geophysicae (1988) (07.04.2016)
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The first case of fatal familial insomnia (FFI) in the Netherlands: a patient from Egyptian descent with concurrent four repeat tau deposits
Jansen, C., Parchi, P., Jelles, B., Gouw, A. A., Beunders, G., van Spaendonk, R. M. L., van de Kamp, J. M., Lemstra, A. W., Capellari, S., Rozemuller, A. J. M.
Published in Neuropathology and applied neurobiology (01.08.2011)
Published in Neuropathology and applied neurobiology (01.08.2011)
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Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophy
Wesdorp, M., Schreur, V., Beynon, A.J., Oostrik, J., van de Kamp, J.M., Elting, M.W., van den Boogaard, M.‐J.H., Feenstra, I., Admiraal, R.J.C., Kunst, H.P.M., Hoyng, C.B., Kremer, H., Yntema, H.G., Pennings, R.J.E., Schraders, M.
Published in Clinical genetics (01.08.2018)
Published in Clinical genetics (01.08.2018)
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Genotype-phenotype correlation of contiguous gene deletions of SLC6A8, BCAP31 and ABCD1
van de Kamp, J.M., Errami, A., Howidi, M., Anselm, I., Winter, S., Phalin-Roque, J., Osaka, H., van Dooren, S.J.M., Mancini, G.M., Steinberg, S.J., Salomons, G.S.
Published in Clinical genetics (01.02.2015)
Published in Clinical genetics (01.02.2015)
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Journal Article
Treatment of osteogenesis imperfecta with the bisphosphonate olpadronate (dimethylaminohydroxypropylidene bisphosphonate)
LANDSMEER-BEKER, E. A, MASSA, G. G, MAASWINKEL-MOOY, P. D, VAN DE KAMP, J. J. P, PAPAPOULOS, S. E
Published in European journal of pediatrics (01.10.1997)
Published in European journal of pediatrics (01.10.1997)
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Journal Article
Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardation
Bijlsma, E.K, Collins, A, Papa, F.T, Tejada, M.I, Wheeler, P, Peeters, E.A.J, Gijsbers, A.C.J, van de Kamp, J.M, Kriek, M, Losekoot, M, Broekma, A.J, Crolla, J.A, Pollazzon, M, Mucciolo, M, Katzaki, E, Disciglio, V, Ferreri, M.I, Marozza, A, Mencarelli, M.A, Castagnini, C, Dosa, L, Ariani, F, Mari, F, Canitano, R, Hayek, G, Botella, M.P, Gener, B, Mínguez, M, Renieri, A, Ruivenkamp, C.A.L
Published in European journal of medical genetics (01.06.2012)
Published in European journal of medical genetics (01.06.2012)
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Exome variant prioritization in a large cohort of hearing-impaired individuals indicates IKZF2 to be associated with non-syndromic hearing loss and guides future research of unsolved cases
Velde, Hedwig M., Vaseghi-Shanjani, Maryam, Smits, Jeroen J., Ramakrishnan, Gayatri, Oostrik, Jaap, Wesdorp, Mieke, Astuti, Galuh, Yntema, Helger G., Hoefsloot, Lies, Lanting, Cris P., Huynen, Martijn A., Lehman, Anna, Turvey, Stuart E., Pennings, Ronald J. E., Kremer, Hannie
Published in Human genetics (01.11.2024)
Published in Human genetics (01.11.2024)
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The natural history and genotype–phenotype correlations of TMPRSS3 hearing loss: an international, multi-center, cohort analysis
Colbert, Brett M., Lanting, Cris, Smeal, Molly, Blanton, Susan, Dykxhoorn, Derek M., Tang, Pei-Ciao, Getchell, Richard L., Velde, Hedwig, Fehrmann, Mirthe, Thorpe, Ryan, Chapagain, Prem, Elkhaligy, Heidy, Kremer, Hannie, Yntema, Helger, Haer-Wigman, Lonneke, Redfield, Shelby, Sun, Tieqi, Bruijn, Saskia, Plomp, Astrid, Goderie, Thadé, van de Kamp, Jiddeke, Free, Rolien H., Wassink-Ruiter, Jolien Klein, Widdershoven, Josine, Vanhoutte, Els, Rotteveel, Liselotte, Kriek, Marjolein, van Dooren, Marieke, Hoefsloot, Lies, de Gier, Heriette H. W., Schaefer, Amanda, Kolbe, Diana, Azaiez, Hela, Rabie, Grace, Aburayyan, Armal, Kawas, Mariana, Kanaan, Moien, Holder, Jourdan, Usami, Shin-ichi, Chen, Zhengyi, Dai, Pu, Holt, Jeffrey, Nelson, Rick, Choi, Byung Yoon, Shearer, Eliot, Smith, Richard J. H., Pennings, Ronald, Liu, Xue Zhong
Published in Human genetics (01.05.2024)
Published in Human genetics (01.05.2024)
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Journal Article
Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant
Smits, Jeroen J., de Bruijn, Suzanne E., Lanting, Cornelis P., Oostrik, Jaap, O’Gorman, Luke, Mantere, Tuomo, Cremers, Frans P. M., Roosing, Susanne, Yntema, Helger G., de Vrieze, Erik, Derks, Ronny, Hoischen, Alexander, Pegge, Sjoert A. H., Neveling, Kornelia, Pennings, Ronald J. E., Kremer, Hannie
Published in Human genetics (01.04.2022)
Published in Human genetics (01.04.2022)
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Journal Article
Correction to: Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant
Smits, Jeroen J., de Bruijn, Suzanne E., Lanting, Cornelis P., Oostrik, Jaap, O’Gorman, Luke, Mantere, Tuomo, Cremers, Frans P. M., Roosing, Susanne, Yntema, Helger G., de Vrieze, Erik, Derks, Ronny, Hoischen, Alexander, Pegge, Sjoert A. H., Neveling, Kornelia, Pennings, Ronald J. E., Kremer, Hannie
Published in Human genetics (01.04.2022)
Published in Human genetics (01.04.2022)
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Journal Article
Mesenchymal stem cells can be recruited to wounded tissue via hepatocyte growth factor‐loaded biomaterials
Kamp, J., Paefgen, V., Wöltje, M., Böbel, M., Jaekel, J., Rath, B., Labude, N., Knüchel, R., Jahnen‐Dechent, W., Neuss, Sabine
Published in Journal of tissue engineering and regenerative medicine (01.11.2017)
Published in Journal of tissue engineering and regenerative medicine (01.11.2017)
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Evaluation of the outcome of CT and MR imaging in pediatric patients with bilateral sensorineural hearing loss
van Beeck Calkoen, E.A., Merkus, P., Goverts, S.T., van de Kamp, J.M., Mulder, M.F., Sanchez Aliaga, E., Hensen, E.F.
Published in International journal of pediatric otorhinolaryngology (01.05.2018)
Published in International journal of pediatric otorhinolaryngology (01.05.2018)
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Spectra of equatorial total electron content derived from GPS signals
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Conference Proceeding
A large retinoblastoma detected in a fetus at 21 weeks of gestation
Maat-Kievit, J A, Oepkes, D, Hartwig, N G, Vermeij-Keers, C, van Kamp, I L, van de Kamp, J J
Published in Prenatal diagnosis (01.05.1993)
Published in Prenatal diagnosis (01.05.1993)
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