Search Results - "Herms, S"

Immune‐regulatory genes as possible modifiers of familial pityriasis rubra pilaris – lessons from a family with PRP and psoriasis by Spoerri, I., Herms, S., Eytan, O., Sarig, O., Heinimann, K., Sprecher, E., Itin, P.H., Burger, B.

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Strong Association of Variants around FOXE1 and Orofacial Clefting by Ludwig, K.U., Böhmer, A.C., Rubini, M., Mossey, P.A., Herms, S., Nowak, S., Reutter, H., Alblas, M.A., Lippke, B., Barth, S., Paredes-Zenteno, M., Muñoz-Jimenez, S.G., Ortiz-Lopez, R., Kreusch, T., Hemprich, A., Martini, M., Braumann, B., Jäger, A., Pötzsch, B., Molloy, A., Peterlin, B., Hoffmann, P., Nöthen, M.M., Rojas-Martinez, A., Knapp, M., Steegers-Theunissen, R.P., Mangold, E.

“…Nonsyndromic orofacial clefting (nsOFC) is a common, complex congenital disorder. The most frequent forms are nonsyndromic cleft lip with or without cleft…”
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Correlation of fetal scalp blood sampling pH with neonatal outcome umbilical artery pH value by Kuehnle, E., Herms, S., Kohls, F., Kundu, S., Hillemanns, P., Staboulidou, Ismini

“…Purpose Fetal scalp blood sampling is considered as a complimentary tool in addition to cardiotocography to assess fetal well-being. This blood sampling is…”
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Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder by Priebe, L, Degenhardt, F A, Herms, S, Haenisch, B, Mattheisen, M, Nieratschker, V, Weingarten, M, Witt, S, Breuer, R, Paul, T, Alblas, M, Moebus, S, Lathrop, M, Leboyer, M, Schreiber, S, Grigoroiu-Serbanescu, M, Maier, W, Propping, P, Rietschel, M, Nöthen, M M, Cichon, S, Mühleisen, T W

“…We used genome-wide single nucleotide polymorphism (SNP) data to search for the presence of copy number variants (CNVs) in 882 patients with bipolar disorder…”
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Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder by Hughes, Timothy, Sønderby, Ida E., Polushina, Tatiana, Hansson, Lars, Holmgren, Asbjørn, Athanasiu, Lavinia, Melbø-Jørgensen, Christian, Hassani, Sahar, Hoeffding, Louise K., Herms, Stefan, Bergen, Sarah E., Karlsson, Robert, Song, Jie, Rietschel, Marcella, Nöthen, Markus M., Forstner, Andreas J., Hoffmann, Per, Hultman, Christina M., Landén, Mikael, Cichon, Sven, Werge, Thomas, Andreassen, Ole A., Le Hellard, Stephanie, Djurovic, Srdjan

“…Ankyrin-3 (ANK3) is one of the few genes that have been consistently identified as associated with bipolar disorder by multiple genome-wide association…”
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Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss by Redler, S., Brockschmidt, F.F., Tazi-Ahnini, R., Drichel, D., Birch, M.P., Dobson, K., Giehl, K.A., Herms, S., Refke, M., Kluck, N., Kruse, R., Lutz, G., Wolff, H., Böhm, M., Becker, T., Nöthen, M.M., Messenger, A.G., Betz, R.C.

“…Summary Background  The aetiology of female pattern hair loss (FPHL) is largely unknown. However, it is hypothesized that FPHL and male pattern baldness (AGA)…”
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Exome chip analyses in adult attention deficit hyperactivity disorder by Zayats, T, Jacobsen, K K, Kleppe, R, Jacob, C P, Kittel-Schneider, S, Ribasés, M, Ramos-Quiroga, J A, Richarte, V, Casas, M, Mota, N R, Grevet, E H, Klein, M, Corominas, J, Bralten, J, Galesloot, T, Vasquez, A A, Herms, S, Forstner, A J, Larsson, H, Breen, G, Asherson, P, Gross-Lesch, S, Lesch, K P, Cichon, S, Gabrielsen, M B, Holmen, O L, Bau, C H D, Buitelaar, J, Kiemeney, L, Faraone, S V, Cormand, B, Franke, B, Reif, A, Haavik, J, Johansson, S

“…Attention-deficit/hyperactivity disorder (ADHD) is a highly heritable childhood-onset neuropsychiatric condition, often persisting into adulthood. The genetic…”
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The transcriptome of the human mast cell leukemia cells HMC-1.2: an approach to identify specific changes in the gene expression profile in KitD816V systemic mastocytosis by Haenisch, B., Herms, S., Molderings, G. J.

“…To circumvent the costly isolation procedure associated with tissue mast cells, human mast cell lines such as HMC-1 are employed in mastocytosis research, but…”
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GWAS‐based pathway analysis differentiates between fluid and crystallized intelligence by Christoforou, A., Espeseth, T., Davies, G., Fernandes, C. P. D., Giddaluru, S., Mattheisen, M., Tenesa, A., Harris, S. E., Liewald, D. C., Payton, A., Ollier, W., Horan, M., Pendleton, N., Haggarty, P., Djurovic, S., Herms, S., Hoffman, P., Cichon, S., Starr, J. M., Lundervold, A., Reinvang, I., Steen, V. M., Deary, I. J., Le Hellard, S.

“…Cognitive abilities vary among people. About 40–50% of this variability is due to general intelligence (g), which reflects the positive correlation among…”
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Transgenic mouse model of IgM+ lymphoproliferative disease mimicking Waldenström macroglobulinemia by Tompkins, V S, Sompallae, R, Rosean, T R, Walsh, S, Acevedo, M, Kovalchuk, A L, Han, S-S, Jing, X, Holman, C, Rehg, J E, Herms, S, Sunderland, J S, Morse, H C, Janz, S

“…Waldenström macroglobulinemia (WM) is a low-grade incurable immunoglobulin M + (IgM + ) lymphoplasmacytic lymphoma for which a genetically engineered mouse…”
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P01-42 - G72/G30 candidate gene for bipolar I disorder is not associated with psychosis in the Romanian population by Grigoroiu-Serbanescu, M, Herms, S, Diaconu, C.C, Bleotu, C, Neagu, A.I, Abou Jamra, R, Gherghel, M, Sima, D, Dan, I.A, Prelipceanu, D, Nöthen, M.M, Cichon, S

“…Background The G72/G30 gene is one of the common loci shared both by schizophrenia and bipolar disorder. Studies accumulating since the discovery of this gene…”
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P01-192 Tryptophan hydroxylase 2 (TPH2) gene in bipolar I disorder in the romanian population by Grigoroiu-Serbanescu, M, Diaconu, C.C, Herms, S, Vollmer, J, Bleotu, C, Noethen, M.M, Cichon, S

“…Objective Since the discovery of the tryptophan hydroxylase 2 gene (TPH2) several studies reported association of TPH2 genetic variation with bipolar I…”
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FC02-01 Bipolar and unipolar major depression are not associated with the P2RX7-gene (SNP rs2230912) in an European case-control sample by Grigoroiu-Serbanescu, M, Herms, S, Georgi, A, Hauser, J, Czerski, P, Diaconu, C.C, Babadjanova, G, Jamra, R. Abou, Rietschel, M, Noethen, M.M, Cichon, S

“…Background In two recent studies the SNP rs2230912 (Gln460Arg) located in exon 13 of P2RX7-gene (chromosome 12q24) provided the strongest evidence of…”
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The penetration of ciprofloxacin into human pancreatic and peripancreatic necroses in acute necrotizing pancreatitis by ADAM, U, HERMS, S, WERNER, U, STRUBELT, H, MAKOWIEC, F, HOPT, U. T, DREWELOW, B

“…Antibiotic prophylaxis in necrotizing pancreatitis has recently gained acceptance. Published studies, however, used different antibiotic regimes and some…”
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Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk by Fischer, Annegret, Ellinghaus, David, Nutsua, Marcel, Hofmann, Sylvia, Montgomery, Courtney G, Iannuzzi, Michael C, Rybicki, Benjamin A, Petrek, Martin, Mrazek, Frantisek, Pabst, Stefan, Grohé, Christian, Grunewald, Johan, Ronninger, Marcus, Eklund, Anders, Padyukov, Leonid, Mihailovic-Vucinic, Violeta, Jovanovic, Dragana, Sterclova, Martina, Homolka, Jiri, Nöthen, Markus M, Herms, Stefan, Gieger, Christian, Strauch, Konstantin, Winkelmann, Juliane, Boehm, Bernhard O, Brand, Stephan, Büning, Carsten, Schürmann, Manfred, Ellinghaus, Eva, Baurecht, Hansjörg, Lieb, Wolfgang, Nebel, Almut, Müller-Quernheim, Joachim, Franke, Andre, Schreiber, Stefan

“…Genetic variation plays a significant role in the etiology of sarcoidosis. However, only a small fraction of its heritability has been explained so far. To…”
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225 Defects in immune regulatory genes in a family with familial pityriasis rubra pilaris – novel hints for disease mechanism by Spoerri, I., Herms, S., Eytan, O., Sarig, O., Sprecher, E., Itin, P., Burger, B.

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GWAS for executive function and processing speed suggests involvement of the CADM2 gene by Ibrahim-Verbaas, C A, Bressler, J, Schuur, M, Davies, G, Trompet, S, Smith, J A, Liu, Y, Vitart, V, Petrovic, K, Polasek, O, Zgaga, L, Fawns-Ritchie, C, Hoffmann, P, Karjalainen, J, Lahti, J, Llewellyn, D J, Schmidt, C O, Mather, K A, Chouraki, V, Resnick, S M, Rose, L M, Oldmeadow, C, Stewart, M, deJager, P L, Harris, T B, Liewald, D C, Amin, N, Coker, L H, Stegle, O, Lopez, O L, Teumer, A, Ford, I, Karbalai, N, Becker, J T, Jonsdottir, M K, Au, R, Fehrmann, R S N, Herms, S, Nalls, M, Yaffe, K, Lohman, K, van Swieten, J C, Kardia, S L R, Knopman, D S, Meeks, W M, Heiss, G, Holliday, E G, Tanaka, T, Stott, D J, Wang, J, Ridker, P, Pattie, A, Starr, J M, Hocking, L J, Armstrong, N J, McLachlan, S, Shulman, J M, Eiriksdottir, G, Scott, R J, Kochan, N A, Palotie, A, Hsieh, Y-C, Penman, A, Gottesman, R F, Yu, L, Beiser, A, Garcia, M, Rotter, J I, Slagboom, P E, Westendorp, R G J, Buckley, B M, Wolf, P A, Uitterlinden, A G, Grabe, H J, Bandinelli, S, Chasman, D I, Grodstein, F, Räikkönen, K, Porteous, D J, Price, J F, Sachdev, P S, Ferrucci, L, Attia, J R, Rudan, I, Hayward, C, Wright, A F, Wilson, J F, Cichon, S, Schmidt, H, Ding, J, de Craen, A J M, Fornage, M, Bennett, D A, Deary, I J, Ikram, M A, Launer, L J, Fitzpatrick, A L, Seshadri, S, van Duijn, C M, Mosley, T H

“…To identify common variants contributing to normal variation in two specific domains of cognitive functioning, we conducted a genome-wide association study…”
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The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25 000 subjects by Peyrot, W J, Lee, S H, Milaneschi, Y, Abdellaoui, A, Byrne, E M, Esko, T, de Geus, E J C, Hemani, G, Hottenga, J J, Kloiber, S, Levinson, D F, Lucae, S, Martin, N G, Medland, S E, Metspalu, A, Milani, L, Noethen, M M, Potash, J B, Rietschel, M, Rietveld, C A, Ripke, S, Shi, J, Willemsen, G, Zhu, Z, Boomsma, D I, Wray, N R, Penninx, B W J H

“…An association between lower educational attainment (EA) and an increased risk for depression has been confirmed in various western countries. This study…”
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The transcriptome of the human mast cell leukemia cells HMC-1.2: an approach to identify specific changes in the gene expression profile in Kit super(D816V) systemic mastocytosis by Haenisch, B, Herms, S, Molderings, G J

“…To circumvent the costly isolation procedure associated with tissue mast cells, human mast cell lines such as HMC-1 are employed in mastocytosis research, but…”
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The transcriptome of the human mast cell leukemia cells HMC-1.2: an approach to identify specific changes in the gene expression profile in Kit^sup D816V^ systemic mastocytosis by Haenisch, B, Herms, S, Molderings, G J

“…To circumvent the costly isolation procedure associated with tissue mast cells, human mast cell lines such as HMC-1 are employed in mastocytosis research, but…”
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