Gaucher disease in the COVID-19 pandemic environment: The good, the bad and the unknown by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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... by 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 by 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 by 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 by 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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Rare missense neuronal cadherin gene (CDH2) variants in specific obsessive-compulsive disorder and Tourette disorder phenotypes by 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 by 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 by 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 by 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 by 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 by Orvisky, Eduard, Park, Joseph K, LaMarca, Mary E, Ginns, Edward I, Martin, Brian M, Tayebi, Nahid, Sidransky, Ellen

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Therapy for Gaucher disease: Don’t stop thinking about tomorrow by Sidransky, Ellen, LaMarca, Mary E., Ginns, Edward I.

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Isolation and characterization of the human tyrosine hydroxylase gene: identification of 5' alternative splice sites responsible for multiple mRNAs by O'Malley, Karen L, Anhalt, Michael J, Martin, Brian M, Kelsoe, John R, Winfield, Susan L, Ginns, Edward I

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