Gaucher disease in the COVID-19 pandemic environment: The good, the bad and the unknown von Ginns, Edward I., Ryan, Emory, Sidransky, Ellen

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A new glucocerebrosidase-deficient neuronal cell model provides a tool to probe pathophysiology and therapeutics for Gaucher disease von Westbroek, Wendy, Nguyen, Matthew, Siebert, Marina, Lindstrom, Taylor, Burnett, Robert A, Aflaki, Elma, Jung, Olive, Tamargo, Rafael, Rodriguez-Gil, Jorge L, Acosta, Walter, Hendrix, An, Behre, Bahafta, Tayebi, Nahid, Fujiwara, Hideji, Sidhu, Rohini, Renvoise, Benoit, Ginns, Edward I, Dutra, Amalia, Pak, Evgenia, Cramer, Carole, Ory, Daniel S, Pavan, William J, Sidransky, Ellen

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DNA Methylation Signatures of Early Childhood Malnutrition Associated With Impairments in Attention and Cognition von Peter, Cyril J, Fischer, Laura K, Kundakovic, Marija, Garg, Paras, Jakovcevski, Mira, Dincer, Aslihan, Amaral, Ana C, Ginns, Edward I, Galdzicka, Marzena, Bryce, Cyralene P, Ratner, Chana, Waber, Deborah P, Mokler, David, Medford, Gayle, Champagne, Frances A, Rosene, Douglas L, McGaughy, Jill A, Sharp, Andrew J, Galler, Janina R, Akbarian, Schahram

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Gaucher disease and SARS-CoV-2 infection: Emerging management challenges von Mistry, Pramod, Balwani, Manisha, Barbouth, Deborah, Burrow, T. Andrew, Ginns, Edward I., Goker-Alpan, Ozlem, Grabowski, Gregory A., Kartha, Reena V., Kishnani, Priya S., Lau, Heather, Lee, Chung U., Lopez, Grisel, Maegawa, Gustavo, Packman, Seymour, Prada, Carlos, Rosenbloom, Barry, Lal, Tamanna Roshan, Schiffmann, Rapheal, Weinreb, Neal, Sidransky, Ellen

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DNA Targeting of Rhinal Cortex D2 Receptor Protein Reversibly Blocks Learning of Cues That Predict Reward von Liu, Zheng, Richmond, Barry J., Murray, Elisabeth A., Saunders, Richard C., Steenrod, Sara, Stubblefield, Barbara K., Montague, Deidra M., Ginns, Edward I., Mishkin, Mortimer

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High-Throughput Mass Spectrometry Assay for Quantifying β-Amyloid 40 and 42 in Cerebrospinal Fluid von Weber, Darren M, Tran, Diana, Goldman, Scott M, Taylor, Steven W, Ginns, Edward I, Lagier, Robert J, Rissman, Robert A, Brewer, James B, Clarke, Nigel J

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Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy von Cogné, Benjamin, Latypova, Xenia, Senaratne, Lokuliyanage Dona Samudita, Martin, Ludovic, Koboldt, Daniel C., Kellaris, Georgios, Fievet, Lorraine, Le Meur, Guylène, Caldari, Dominique, Debray, Dominique, Nizon, Mathilde, Frengen, Eirik, Bowne, Sara J., Buckley, Reuben M., Aberdein, Danielle, Alves, Paulo C., Barsh, Gregory S., Bellone, Rebecca R., Bergström, Tomas F., Boyko, Adam R., Brockman, Jeffrey A., Casal, Margret L., Castelhano, Marta G., Distl, Ottmar, Dodman, Nicholas H., Ellinwood, N. Matthew, Fogle, Jonathan E., Forman, Oliver P., Garrick, Dorian J., Ginns, Edward I., Häggström, Jens, Harvey, Robert J., Hasegawa, Daisuke, Haase, Bianca, Helps, Christopher R., Hernandez, Isabel, Hytönen, Marjo K., Kaukonen, Maria, Kaelin, Christopher B., Kosho, Tomoki, Leclerc, Emilie, Lear, Teri L., Leeb, Tosso, Li, Ronald H.L., Lohi, Hannes, Longeri, Maria, Magnuson, Mark A., Malik, Richard, Mane, Shrinivas P., Munday, John S., Murphy, William J., Pedersen, Niels C., Rothschild, Max F., Rusbridge, Clare, Shapiro, Beth, Stern, Joshua A., Swanson, William F., Terio, Karen A., Todhunter, Rory J., Warren, Wesley C., Wilcox, Elizabeth A., Wildschutte, Julia H., Yu, Yoshihiko, Cadena, Elizabeth L., Daiger, Stephen P., Bujakowska, Kinga M., Pierce, Eric A., Gorin, Michael, Katsanis, Nicholas, Bézieau, Stéphane, Petersen-Jones, Simon M., Occelli, Laurence M., Lyons, Leslie A., Legeai-Mallet, Laurence, Sullivan, Lori S., Davis, Erica E., Isidor, Bertrand

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Neuroinflammation and α-synuclein accumulation in response to glucocerebrosidase deficiency are accompanied by synaptic dysfunction von Ginns, Edward I., Mak, Sally K.-K., Ko, Novie, Karlgren, Juliane, Akbarian, Schahram, Chou, Vivian P., Guo, Yin, Lim, Arlene, Samuelsson, Steven, LaMarca, Mary L., Vazquez-DeRose, Jacqueline, Manning-Boğ, Amy B.

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Cost Effectiveness of Karyotyping, Chromosomal Microarray Analysis, and Targeted Next-Generation Sequencing of Patients with Unexplained Global Developmental Delay or Intellectual... von Li, Yonghong, Anderson, Lori A., Ginns, Edward I., Devlin, James J.

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Applications and efficiencies of the first cat 63K DNA array von Gandolfi, Barbara, Alhaddad, Hasan, Abdi, Mona, Bach, Leslie H., Creighton, Erica K., Davis, Brian W., Decker, Jared E., Dodman, Nicholas H., Ginns, Edward I., Grahn, Jennifer C., Grahn, Robert A., Haase, Bianca, Haggstrom, Jens, Hamilton, Michael J., Helps, Christopher R., Kurushima, Jennifer D., Lohi, Hannes, Longeri, Maria, Malik, Richard, Meurs, Kathryn M., Montague, Michael J., Mullikin, James C., Murphy, William J., Nilson, Sara M., Pedersen, Niels C., Peterson, Carlyn B., Rusbridge, Clare, Saif, Rashid, Shelton, G. Diane, Warren, Wesley C., Wasim, Muhammad, Lyons, Leslie A.

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Glucocerebrosidase haploinsufficiency in A53T α-synuclein mice impacts disease onset and course von Tayebi, Nahid, Parisiadou, Loukia, Berhe, Bahafta, Gonzalez, Ashley N., Serra-Vinardell, Jenny, Tamargo, Raphael J., Maniwang, Emerson, Sorrentino, Zachary, Fujiwara, Hideji, Grey, Richard J., Hassan, Shahzeb, Blech-Hermoni, Yotam N., Chen, Chuyu, McGlinchey, Ryan, Makariou-Pikis, Chrissy, Brooks, Mieu, Ginns, Edward I., Ory, Daniel S., Giasson, Benoit I., Sidransky, Ellen

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Multi-omic analyses in Abyssinian cats with primary renal amyloid deposits von Genova, Francesca, Nonnis, Simona, Maffioli, Elisa, Tedeschi, Gabriella, Strillacci, Maria Giuseppina, Carisetti, Michela, Sironi, Giuseppe, Cupaioli, Francesca Anna, Di Nanni, Noemi, Mezzelani, Alessandra, Mosca, Ettore, Helps, Christopher R., Leegwater, Peter A. J., Dorso, Laetitia, Longeri, Maria

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A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish von Ginns, Edward I, Egeland, Janice A, Paul, Steven M, Ott, Jurg, Pauls, David L, Keith, Tim P, Weissenbach, Jean, Fann, Cathy S.J, Falls, Kathleen M, Carulli, John P, Allen, Cleona R

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Rare missense neuronal cadherin gene (CDH2) variants in specific obsessive-compulsive disorder and Tourette disorder phenotypes von Moya, Pablo R, Dodman, Nicholas H, Timpano, Kiara R, Rubenstein, Liza M, Rana, Zaker, Fried, Ruby L, Reichardt, Louis F, Heiman, Gary A, Tischfield, Jay A, King, Robert A, Galdzicka, Marzena, Ginns, Edward I, Wendland, Jens R

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Author Correction: Applications and efficiencies of the first cat 63 K DNA array von Gandolfi, Barbara, Alhaddad, Hasan, Abdi, Mona, Bach, Leslie H., Creighton, Erica K., Davis, Brian W., Decker, Jared E., Dodman, Nicholas H., Ginns, Edward I., Grahn, Jennifer C., Grahn, Robert A., Haase, Bianca, Haggstrom, Jens, Hamilton, Michael J., Helps, Christopher R., Kurushima, Jennifer D., Lohi, Hannes, Longeri, Maria, Malik, Richard, Meurs, Kathryn M., Montague, Michael J., Mullikin, James C., Murphy, William J., Nilson, Sara M., Pedersen, Niels C., Peterson, Carlyn B., Rusbridge, Clare, Saif, Rashid, Shelton, G. Diane, Warren, Wesley C., Wasim, Muhammad, Lyons, Leslie A.

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Skin ultrastructural findings in type 2 Gaucher disease: Diagnostic implications von Chan, Aegean, Holleran, Walter M., Ferguson, Tajh, Crumrine, Debra, Goker-Alpan, Ozlem, Schiffmann, Raphael, Tayebi, Nahid, Ginns, Edward I., Elias, Peter M., Sidransky, Ellen

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Author Correction: Applications and efficiencies of the first cat 63K DNA array von Gandolfi, Barbara, Alhaddad, Hasan, Abdi, Mona, Bach, Leslie H., Creighton, Erica K., Davis, Brian W., Decker, Jared E., Dodman, Nicholas H., Ginns, Edward I., Grahn, Jennifer C., Grahn, Robert A., Haase, Bianca, Haggstrom, Jens, Hamilton, Michael J., Helps, Christopher R., Kurushima, Jennifer D., Lohi, Hannes, Longeri, Maria, Malik, Richard, Meurs, Kathryn M., Montague, Michael J., Mullikin, James C., Murphy, William J., Nilson, Sara M., Pedersen, Niels C., Peterson, Carlyn B., Rusbridge, Clare, Saif, Rashid, Shelton, G. Diane, Warren, Wesley C., Wasim, Muhammad, Lyons, Leslie A.

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A Genome-Wide Search for Chromosomal Loci Linked to Mental Health Wellness in Relatives at High Risk for Bipolar Affective Disorder among the Old Order Amish von Ginns, Edward I., St. Jean, Pamela, Philibert, Robert A., Galdzicka, Marzena, Damschroder-Williams, Patricia, Thiel, Bonnie, Long, Robert T., Ingraham, Loring J., Dalwaldi, Harnisha, Murray, Melissa A., Ehlert, Melissa, Paul, Sharon, Remortel, Brian G., Patel, Ashima P., Maria C. H. Anderson, Shaio, Cary, Lau, Elaine, Dymarskaia, Inna, Martin, Brian M., Stubblefield, Barbara, Falls, Kathleen M., Carulli, John P., Keith, Tim P., Cathy S. J. Fann, Lacy, Lucy G., Allen, Cleona R., Hostetter, Abram M., Elston, Robert C., Schork, Nicholas J., Egeland, Janice A., Paul, Steven M.

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Glucosylsphingosine accumulation in tissues from patients with Gaucher disease: correlation with phenotype and genotype von Orvisky, Eduard, Park, Joseph K, LaMarca, Mary E, Ginns, Edward I, Martin, Brian M, Tayebi, Nahid, Sidransky, Ellen

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Gaucher disease in the neonate : a distinct Gaucher phenotype is analogous to a mouse model created by targeted disruption of the glucocerebrosidase gene von SIDRANSKY, E, SHERER, D. M, GINNS, E. I

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