Search Results - "Bouwkamp, Christian G"

Engram-specific transcriptome profiling of contextual memory consolidation by Rao-Ruiz, Priyanka, Couey, Jonathan J., Marcelo, Ivo M., Bouwkamp, Christian G., Slump, Denise E., Matos, Mariana R., van der Loo, Rolinka J., Martins, Gabriela J., van den Hout, Mirjam, van IJcken, Wilfred F., Costa, Rui M., van den Oever, Michel C., Kushner, Steven A.

“…Sparse populations of neurons in the dentate gyrus (DG) of the hippocampus are causally implicated in the encoding of contextual fear memories. However,…”
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The Zinc Transporter SLC39A7 (ZIP7) Is Essential for Regulation of Cytosolic Zinc Levels by Woodruff, Grace, Bouwkamp, Christian G, de Vrij, Femke M, Lovenberg, Timothy, Bonaventure, Pascal, Kushner, Steven A, Harrington, Anthony W

“…Zinc homeostasis is a highly regulated process in mammalian cells that is critical for normal growth and development. Movement of zinc across cell compartments…”
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Candidate CSPG4 mutations and induced pluripotent stem cell modeling implicate oligodendrocyte progenitor cell dysfunction in familial schizophrenia by de Vrij, Femke M., Bouwkamp, Christian G., Gunhanlar, Nilhan, Shpak, Guy, Lendemeijer, Bas, Baghdadi, Maarouf, Gopalakrishna, Shreekara, Ghazvini, Mehrnaz, Li, Tracy M., Quadri, Marialuisa, Olgiati, Simone, Breedveld, Guido J., Coesmans, Michiel, Mientjes, Edwin, de Wit, Ton, Verheijen, Frans W., Beverloo, H. Berna, Cohen, Dan, Kok, Rob M., Bakker, P. Roberto, Nijburg, Aviva, Spijker, Annet T., Haffmans, P. M. Judith, Hoencamp, Erik, Bergink, Veerle, Vorstman, Jacob A., Wu, Timothy, Olde Loohuis, Loes M., Amin, Najaf, Langen, Carolyn D., Hofman, Albert, Hoogendijk, Witte J., van Duijn, Cornelia M., Ikram, M. Arfan, Vernooij, Meike W., Tiemeier, Henning, Uitterlinden, André G., Elgersma, Ype, Distel, Ben, Gribnau, Joost, White, Tonya, Bonifati, Vincenzo, Kushner, Steven A.

“…Schizophrenia is highly heritable, yet its underlying pathophysiology remains largely unknown. Among the most well-replicated findings in neurobiological…”
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DNAJC6 Mutations Associated With Early-Onset Parkinson's Disease by Olgiati, Simone, Quadri, Marialuisa, Fang, Mingyan, Rood, Janneke P.M.A., Saute, Jonas A., Chien, Hsin Fen, Bouwkamp, Christian G., Graafland, Josja, Minneboo, Michelle, Breedveld, Guido J., Zhang, Jianguo, Verheijen, Frans W., Boon, Agnita J.W., Kievit, Anneke J.A., Jardim, Laura Bannach, Mandemakers, Wim, Barbosa, Egberto Reis, Rieder, Carlos R.M., Leenders, Klaus L., Wang, Jun, Bonifati, Vincenzo

“…Objective DNAJC6 mutations were recently described in two families with autosomal recessive juvenile parkinsonism (onset age < 11), prominent atypical signs,…”
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The levonorgestrel-releasing intrauterine device potentiates stress reactivity by Aleknaviciute, Jurate, Tulen, Joke H.M, De Rijke, Yolanda B, Bouwkamp, Christian G, van der Kroeg, Mark, Timmermans, Mirjam, Wester, Vincent L, Bergink, Veerle, Hoogendijk, Witte J.G, Tiemeier, Henning, van Rossum, Elisabeth F.C, Kooiman, Cornelis G, Kushner, Steven A

“…Highlights • LNG-IUD is associated with a robust potentiation of HPA axis responsivity. • LNG-IUD potentiates the autonomic heart rate response during…”
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Copy Number Variation in Syndromic Forms of Psychiatric Illness: The Emerging Value of Clinical Genetic Testing in Psychiatry by Bouwkamp, Christian G, Kievit, Anneke J.A, Markx, Sander, Friedman, Joseph I, van Zutven, Laura, van Minkelen, Rick, Vrijenhoek, Terry, Xu, Bin, Sterrenburg-van de Nieuwegiessen, Ineke, Veltman, Joris A, Bonifati, Vincenzo, Kushner, Steven A

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A balanced translocation disrupting BCL2L10 and PNLDC1 segregates with affective psychosis by Bouwkamp, Christian G., Kievit, Anneke J. A., Olgiati, Simone, Breedveld, Guido J., Coesmans, Michiel, Bonifati, Vincenzo, Kushner, Steven A.

“…Affective psychoses are a group of severe psychiatric disorders, including schizoaffective disorder and bipolar I disorder, together affecting ∼1% of the…”
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ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia by Bouwkamp, Christian G, Afawi, Zaid, Fattal-Valevski, Aviva, Krabbendam, Inge E, Rivetti, Stefano, Masalha, Rafik, Quadri, Marialuisa, Breedveld, Guido J, Mandel, Hanna, Tailakh, Muhammad Abu, Beverloo, H Berna, Stevanin, Giovanni, Brice, Alexis, van IJcken, Wilfred F J, Vernooij, Meike W, Dolga, Amalia M, de Vrij, Femke M S, Bonifati, Vincenzo, Kushner, Steven A

“…To identify the clinical characteristics and genetic etiology of a family affected with hereditary spastic paraplegia (HSP). Clinical, genetic, and functional…”
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A boy with conduct disorder (CD), attention deficit hyperactivity disorder (ADHD), borderline intellectual disability, and 47,XXY syndrome in combination with a 7q11.23 duplication, 11p15.5 deletion, and 20q13.33 deletion by Kolaitis, Gerasimos, Bouwkamp, Christian G, Papakonstantinou, Alexia, Otheiti, Ioanna, Belivanaki, Maria, Haritaki, Styliani, Korpa, Terpsihori, Albani, Zinovia, Terzioglou, Elena, Apostola, Polyxeni, Skamnaki, Aggeliki, Xaidara, Athena, Kosma, Konstantina, Kitsiou-Tzeli, Sophia, Tzetis, Maria

“…This is a case with multiple chromosomal aberrations which are likely etiological for the observed psychiatric phenotype consisting of attention deficit…”
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DNAJC6 mutations associated with early-onset Parkinson's disease by Olgiati, Simone, Quadri, Marialuisa, Fang, Mingyan, Rood, Janneke P.M.A, Saute, Jonas A, Chien, Hsin Fen, Bouwkamp, Christian G, Graafland, Josja, Minneboo, Michelle, Breedveld, Guido J, Zhang, Jianguo, Verheijen, Frans W, Mandemakers, Wim, Boon, Agnita J.W, Kievit, Anneke J.A, Jardim, Laura Bannach, Barbosa, Egberto Reis, Rieder, Carlos R.M, Leenders, Klaus L, Wang, Jun, Bonifati, Vincenzo

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DNAJC6 mutations associated with early-onset Parkinson's disease by Olgiati, Simone, Quadri, Marialuisa, Fang, Mingyan, Rood, Janneke P.M.A, Saute, Jonas A, Chien, Hsin Fen, Bouwkamp, Christian G, Graafland, Josja, Minneboo, Michelle, Breedveld, Guido J, Zhang, Jianguo, Verheijen, Frans W, Mandemakers, Wim, Boon, Agnita J.W, Kievit, Anneke J.A, Jardim, Laura Bannach, Barbosa, Egberto Reis, Rieder, Carlos R.M, Leenders, Klaus L, Wang, Jun, Bonifati, Vincenzo

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Interpersonal and social rhythm group therapy for patients with bipolar disorder by Bouwkamp, Christian G, de Kruiff, Marije E, van Troost, Thea M, Snippe, Dina, Blom, Marc J, de Winter, Remco F P, Judith Haffmans, P M

“…This article describes Interpersonal and Social Rhythm Therapy (IPSRT) adapted for use in a group setting for patients with bipolar disorder. In a preliminary…”
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D NAJC 6 M utations A ssociated W ith E arly‐ O nset P arkinson's D isease by Olgiati, Simone, Quadri, Marialuisa, Fang, Mingyan, Rood, Janneke P.M.A., Saute, Jonas A., Chien, Hsin Fen, Bouwkamp, Christian G., Graafland, Josja, Minneboo, Michelle, Breedveld, Guido J., Zhang, Jianguo, Verheijen, Frans W., Boon, Agnita J.W., Kievit, Anneke J.A., Jardim, Laura Bannach, Mandemakers, Wim, Barbosa, Egberto Reis, Rieder, Carlos R.M., Leenders, Klaus L., Wang, Jun, Bonifati, Vincenzo

“…Objective DNAJC6 mutations were recently described in two families with autosomal recessive juvenile parkinsonism (onset age < 11), prominent atypical signs,…”
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A boy with conduct disorder , borderline intellectual disability, and 47,XXY syndrome in combination with a 7q11.23 duplication, 11p15.5 deletion, and 20q13.33 deletion by Kolaitis, Gerasimos, Bouwkamp, Christian G, Papakonstantinou, Alexia, Otheiti, Ioanna, Belivanaki, Maria, Haritaki, Styliani, Korpa, Terpsihori, Albani, Zinovia, Terzioglou, Elena, Apostola, Polyxeni, Skamnaki, Aggeliki, Xaidara, Athena, Kosma, Konstantina, Kitsiou-Tzeli, Sophia, Tzetis, Maria

“…This is a case with multiple chromosomal aberrations which are likely etiological for the observed psychiatric phenotype consisting of attention deficit…”
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A boy with conduct disorder (CD), attention deficit hyperactivity disorder (ADHD), borderline intellectual disability, and 47,XXY syndrome in combination with a 7q11.23 duplication, 11p15.5 deletion, and 20q13.33 deletion by Kolaitis, Gerasimos, Bouwkamp, Christian G, Papakonstantinou, Alexia, Otheiti, Ioanna, Belivanaki, Maria, Haritaki, Styliani, Korpa, Terpsihori, Albani, Zinovia, Terzioglou, Elena, Apostola, Polyxeni, Skamnaki, Aggeliki, Xaidara, Athena, Kosma, Konstantina, Kitsiou-Tzeli, Sophia, Tzetis, Maria

“…BACKGROUNDThis is a case with multiple chromosomal aberrations which are likely etiological for the observed psychiatric phenotype consisting of attention…”
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