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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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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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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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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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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Mining the 99 Lives Cat Genome Sequencing Consortium database implicates genes and variants for the Ticked locus in domestic cats (Felis catus) by Lyons, L. A., Buckley, R. M., Harvey, R. J., Abitbol, Marie, Aberdein, Danielle, Alves, Paulo C., Ohlsson Andersson, Asa, Bellone, Rebecca R., Bergström, Tomas F., Bilgen, Nuket, Boyko, Adam R., Brockman, Jeffrey A., Casal, Margret L., Castelhano, Marta G., Davis, Brian W., Davison, Lucy, Distl, Ottmar, Dodman, Nicholas H., Ellinwood, N. Matthew, Fogle, Jonathan E., Forman, Oliver P., Garrick, Dorian J., Ginns, Edward I., Häggström, Jens, Hasegawa, Daisuke, Haase, Bianca, Jagannathan, Vidhya, Lait, Philippa, Hernandez, Isabel, Hytönen, Marjo K., Kaukonen, Maria, Kosho, Tomoki, Leclerc, Emilie, Lear, Teri L., Leeb, Tosso, Li, Ronald H.L., Lohi, Hannes, Longeri, Maria, Magnuson, Mark A., Malik, Richard, Mane, Shrinivasrao P., Middleton, Rondo, Munday, John S., Murphy, William J., Myers, Alexandra N., Pedersen, Niels C., Peterson‐Jones, Simon M., Rothschild, Max F., Rusbridge, Clare, Schoenebeck, Jeffrey J., 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

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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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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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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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T160. Novel Biomarker for Bipolar Disorder: Sonic Hedgehog Protein by Marsh, Wendy, Ginns, Edward

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

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