From the Cradle to the Grave: The Role of Macrophages in Erythropoiesis and Erythrophagocytosis von Klei, Thomas R L, Meinderts, Sanne M, van den Berg, Timo K, van Bruggen, Robin

Volltext

Genetic risk for schizophrenia and psychosis in Alzheimer disease von DeMichele-Sweet, M A A, Weamer, E A, Klei, L, Vrana, D T, Hollingshead, D J, Seltman, H J, Sims, R, Foroud, T, Hernandez, I, Moreno-Grau, S, Tárraga, L, Boada, M, Ruiz, A, Williams, J, Mayeux, R, Lopez, O L, Sibille, E L, Kamboh, M I, Devlin, B, Sweet, R A

Volltext

Recommendations for in vitro evaluation of blood components collected, prepared and stored in non‐DEHP medical devices von Klei, Thomas R. L., Begue, Stephane, Lotens, Anaïs, Sigurjónsson, Ólafur E., Wiltshire, Michael D., George, Chloë, Burg, Peter J. M., Evans, Ryan, Larsson, Linda, Thomas, Stephen, Najdovski, Tome, Handke, Wiebke, Eronen, Juha, Mallas, Birte, Korte, Dirk

Volltext

Genome-wide association study of Alzheimer's disease with psychotic symptoms von Hollingworth, P, Sweet, R, Sims, R, Harold, D, Russo, G, Abraham, R, Stretton, A, Jones, N, Gerrish, A, Chapman, J, Ivanov, D, Moskvina, V, Lovestone, S, Priotsi, P, Lupton, M, Brayne, C, Gill, M, Lawlor, B, Lynch, A, Craig, D, McGuinness, B, Johnston, J, Holmes, C, Livingston, G, Bass, N J, Gurling, H, McQuillin, A, Holmans, P, Jones, L, Devlin, B, Klei, L, Barmada, M M, Demirci, F Y, DeKosky, S T, Lopez, O L, Passmore, P, Owen, M J, O'Donovan, M C, Mayeux, R, Kamboh, M I, Williams, J

Volltext

Allogeneic Serum Eye Drops: A Randomized Clinical Trial to Evaluate the Clinical Effectiveness of Two Drop Sizes von Vermeulen, Christie, van der Burg, Lars L. J., van Geloven, Nan, Eggink, Catharina A., Cheng, Yanny Y. Y., Nuijts, Rudy M. M. A., Wisse, Robert P. L., van Luijk, Chantal M., Nieuwendaal, Carla, Remeijer, Lies, van der Meer, Pieter F., de Korte, Dirk, Klei, Thomas R. L.

Volltext

Correction: Genetic risk for schizophrenia and psychosis in Alzheimer disease von DeMichele-Sweet, M. A. A., Weamer, E. A., Klei, L., Vrana, D. T., Hollingshead, D. J., Seltman, H. J., Sims, R., Foroud, T., Hernandez, I., Moreno-Grau, S., Tárraga, L., Boada, M., Ruiz, A., Williams, J., Mayeux, R., Lopez, O. L., Sibille, E. L., Kamboh, M. I., Devlin, B., Sweet, R. A.

Volltext

Glycophorin-C sialylation regulates Lu/BCAM adhesive capacity during erythrocyte aging von Klei, T.R.L., de Back, D.Z., Asif, P.J., Verkuijlen, P.J.J.H., Veldthuis, M., Ligthart, P.C., Berghuis, J., Clifford, E., Beuger, B.M., van den Berg, T.K., van Zwieten, R., El Nemer, W., van Bruggen, R.

Volltext

Persistent infection with neurotropic herpes viruses and cognitive impairment von Watson, A. M. M., Prasad, K. M., Klei, L., Wood, J. A., Yolken, R. H., Gur, R. C., Bradford, L. D., Calkins, M. E., Richard, J., Edwards, N., Savage, R. M., Allen, T. B., Kwentus, J., McEvoy, J. P., Santos, A. B., Wiener, H. W., Go, R. C. P., Perry, R. T., Nasrallah, H. A., Gur, R. E., Devlin, B., Nimgaonkar, V. L.

Volltext

Genetic analysis of vertebral trabecular bone density and cross-sectional area in older men von Zmuda, J. M., Yerges-Armstrong, L. M., Moffett, S. P., Klei, L., Kammerer, C. M., Roeder, K., Cauley, J. A., Kuipers, A., Ensrud, K. E., Nestlerode, C. S., Hoffman, A. R., Lewis, C. E., Lang, T. F., Barrett-Connor, E., Ferrell, R. E., Orwoll, E. S.

Volltext

Low Levels of Arsenic Trioxide Stimulate Proliferative Signals in Primary Vascular Cells without Activating Stress Effector Pathways von Barchowsky, Aaron, Roussel, Robert R., Klei, Linda R., James, Philip E., Ganju, Neema, Smith, Karol R., Dudek, Edward J.

Volltext

Amino acid position 11 of HLA-DR beta 1 is a major determinant of chromosome 6p association with ulcerative colitis von Achkar, J-P, Klei, L, Bakker, P I W de, Bellone, G, Rebert, N, Scott, R, Lu, Y, Regueiro, M, Brzezinski, A, Kamboh, M I, Fiocchi, C, Devlin, B, Trucco, M, Ringquist, S, Roeder, K, Duerr, R H

Volltext

Amino acid position 11 of HLA-DRβ1 is a major determinant of chromosome 6p association with ulcerative colitis von Achkar, J-P, Klei, L, Bakker, P I W de, Bellone, G, Rebert, N, Scott, R, Lu, Y, Regueiro, M, Brzezinski, A, Kamboh, M I, Fiocchi, C, Devlin, B, Trucco, M, Ringquist, S, Roeder, K, Duerr, R H

Volltext

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism von Fu, Jack M., Satterstrom, F. Kyle, Peng, Minshi, Brand, Harrison, Collins, Ryan L., Dong, Shan, Wamsley, Brie, Klei, Lambertus, Wang, Lily, Hao, Stephanie P., Stevens, Christine R., Cusick, Caroline, Babadi, Mehrtash, Banks, Eric, Collins, Brett, Dodge, Sheila, Gabriel, Stacey B., Gauthier, Laura, Lee, Samuel K., Liang, Lindsay, Ljungdahl, Alicia, Mahjani, Behrang, Sloofman, Laura, Smirnov, Andrey N., Barbosa, Mafalda, Betancur, Catalina, Brusco, Alfredo, Chung, Brian H. Y., Cook, Edwin H., Cuccaro, Michael L., Domenici, Enrico, Ferrero, Giovanni Battista, Gargus, J. Jay, Herman, Gail E., Hertz-Picciotto, Irva, Maciel, Patricia, Manoach, Dara S., Passos-Bueno, Maria Rita, Persico, Antonio M., Renieri, Alessandra, Sutcliffe, James S., Tassone, Flora, Trabetti, Elisabetta, Campos, Gabriele, Cardaropoli, Simona, Carli, Diana, Chan, Marcus C. Y., Fallerini, Chiara, Giorgio, Elisa, Girardi, Ana Cristina, Hansen-Kiss, Emily, Lee, So Lun, Lintas, Carla, Ludena, Yunin, Nguyen, Rachel, Pavinato, Lisa, Pericak-Vance, Margaret, Pessah, Isaac N., Schmidt, Rebecca J., Smith, Moyra, Costa, Claudia I. S., Trajkova, Slavica, Wang, Jaqueline Y. T., Yu, Mullin H. C., Cutler, David J., De Rubeis, Silvia, Buxbaum, Joseph D., Daly, Mark J., Devlin, Bernie, Roeder, Kathryn, Sanders, Stephan J., Talkowski, Michael E.

Volltext

Hemolysis in the spleen drives erythrocyte turnover von Klei, T.R.L, Dalimot, J., Nota, B., Veldthuis, M., Mul, F.P.J, Rademakers, T., Hoogenboezem, M., Nagelkerke, S.Q., van IJcken, W.F.J, Oole, E., Svendsen, P., Moestrup, S.K., van Alphen, F.P.J, Meijer, A.B., Kuijpers, T.W., van Zwieten, R., van Bruggen, R.

Volltext

Differential activity of transcribed enhancers in the prefrontal cortex of 537 cases with schizophrenia and controls von Hauberg, Mads E., Fullard, John F., Zhu, Lingxue, Cohain, Ariella T., Giambartolomei, Claudia, Misir, Ruth, Reach, Sarah, Johnson, Jessica S., Wang, Minghui, Mattheisen, Manuel, Børglum, Anders Dupont, Zhang, Bin, Sieberts, Solveig K., Peters, Mette A., Domenici, Enrico, Schadt, Eric E., Devlin, Bernie, Sklar, Pamela, Roeder, Kathryn, Roussos, Panos

Volltext

Arsenite stimulates plasma membrane NADPH oxidase in vascular endothelial cells von Smith, Karol R, Klei, Linda R, Barchowsky, Aaron

Volltext

Human and murine splenic neutrophils are potent phagocytes of IgG-opsonized red blood cells von Meinderts, Sanne M., Oldenborg, Per-Arne, Beuger, Boukje M., Klei, Thomas R.L., Johansson, Johanna, Kuijpers, Taco W., Matozaki, Takashi, Huisman, Elise J., de Haas, Masja, van den Berg, Timo K., van Bruggen, Robin

Volltext

Synaptic, transcriptional and chromatin genes disrupted in autism von De Rubeis, Silvia, He, Xin, Goldberg, Arthur P., Poultney, Christopher S., Samocha, Kaitlin, Ercument Cicek, A., Kou, Yan, Liu, Li, Fromer, Menachem, Walker, Susan, Singh, Tarjinder, Klei, Lambertus, Kosmicki, Jack, Fu, Shih-Chen, Aleksic, Branko, Biscaldi, Monica, Bolton, Patrick F., Brownfeld, Jessica M., Cai, Jinlu, Campbell, Nicholas G., Carracedo, Angel, Chahrour, Maria H., Chiocchetti, Andreas G., Coon, Hilary, Crawford, Emily L., Crooks, Lucy, Curran, Sarah R., Dawson, Geraldine, Duketis, Eftichia, Fernandez, Bridget A., Gallagher, Louise, Geller, Evan, Guter, Stephen J., Sean Hill, R., Ionita-Laza, Iuliana, Jimenez Gonzalez, Patricia, Kilpinen, Helena, Klauck, Sabine M., Kolevzon, Alexander, Lee, Irene, Lei, Jing, Lehtimäki, Terho, Lin, Chiao-Feng, Ma’ayan, Avi, Marshall, Christian R., McInnes, Alison L., Neale, Benjamin, Owen, Michael J., Ozaki, Norio, Parellada, Mara, Parr, Jeremy R., Purcell, Shaun, Puura, Kaija, Rajagopalan, Deepthi, Rehnström, Karola, Reichenberg, Abraham, Sabo, Aniko, Sachse, Michael, Sanders, Stephan J., Schafer, Chad, Schulte-Rüther, Martin, Skuse, David, Stevens, Christine, Szatmari, Peter, Tammimies, Kristiina, Valladares, Otto, Voran, Annette, Wang, Li-San, Weiss, Lauren A., Jeremy Willsey, A., Yu, Timothy W., Yuen, Ryan K. C., Cook, Edwin H., Freitag, Christine M., Gill, Michael, Hultman, Christina M., Lehner, Thomas, Palotie, Aarno, Schellenberg, Gerard D., Sklar, Pamela, State, Matthew W., Sutcliffe, James S., Walsh, Christopher A., Scherer, Stephen W., Zwick, Michael E., Barrett, Jeffrey C., Cutler, David J., Roeder, Kathryn, Devlin, Bernie, Daly, Mark J., Buxbaum, Joseph D.

Volltext

A Simple Method for Weighted Bending of Genetic (Co)variance Matrices von Jorjani, H, Klei, L, Emanuelson, U

Volltext

Most genetic risk for autism resides with common variation von Gaugler, Trent, Klei, Lambertus, Sanders, Stephan J, Bodea, Corneliu A, Goldberg, Arthur P, Lee, Ann B, Mahajan, Milind, Manaa, Dina, Pawitan, Yudi, Reichert, Jennifer, Ripke, Stephan, Sandin, Sven, Sklar, Pamela, Svantesson, Oscar, Reichenberg, Abraham, Hultman, Christina M, Devlin, Bernie, Roeder, Kathryn, Buxbaum, Joseph D

Volltext