Factors Influencing Entrepreneurial Dietitians in the Use of the Computer as a Professional Tool by JOHNSON, THERESA ELAINE, BORJA, MARIANNE E., LOFTUS, MARIE K., McCLINTOCK, N.KAY

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Association between childhood maltreatment and the clinical course of bipolar disorders: A survival analysis of mood recurrences by Grillault Laroche, Diane, Godin, Ophélia, Belzeaux, Raoul, M’Bailara, Katia, Loftus, Joséphine, Courtet, Philippe, Dubertret, Caroline, Haffen, Emmanuel, Llorca, Pierre Michel, Olie, Emilie, Passerieux, Christine, Polosan, Mircea, Schwan, Raymund, Leboyer, Marion, Bellivier, Frank, Marie‐Claire, Cynthia, Etain, Bruno

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Cell-type-specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes by Zhang, Tongwu, Choi, Jiyeon, Kovacs, Michael A, Shi, Jianxin, Xu, Mai, Goldstein, Alisa M, Trower, Adam J, Bishop, D Timothy, Iles, Mark M, Duffy, David L, MacGregor, Stuart, Amundadottir, Laufey T, Law, Matthew H, Loftus, Stacie K, Pavan, William J, Brown, Kevin M

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Population-level correlates of preterm delivery among black and white women in the U.S by Carmichael, Suzan L, Cullen, Mark R, Mayo, Jonathan A, Gould, Jeffrey B, Loftus, Pooja, Stevenson, David K, Wise, Paul H, Shaw, Gary M

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Outcomes for bipolar patients assessed in the French expert center network: A 2‐year follow‐up observational study (FondaMental Advanced Centers of Expertise for Bipolar Disorder [... by Henry, Chantal, Godin, Ophelia, Courtet, Philippe, Azorin, Jean‐Michel, Gard, Sébastien, Bellivier, Frank, Polosan, Mircea, Kahn, Jean‐Pierre, Roux, Paul, Aubin, Valerie, Costagliola, Dominique, Leboyer, Marion, Etain, Bruno, Laouamri, H, Souyris, K, Barteau, V, Geoffroy, PA, Raust, A, Belzeaux, R., Loftus, J, Sportiche, S, Aouizerate, B, Olié, E, Ducasse, D, Viglianese, N, Lescalier, L, Cohen, RF, Wajsbrot‐Elgrabli, O, Garçon, S, M’Bailara, Katia, Hardy‐Bayle, Marie‐Christine, Grevin, I

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Does BioAge identify accelerated aging in individuals with bipolar disorder? An exploratory study in the FACE‐BD cohort by Etain, Bruno, Marie‐Claire, Cynthia, Spano, Luana, Bellivier, Frank, Leboyer, Marion, Gard, Sébastien, Lefrere, Antoine, Belzeaux, Raoul, Courtet, Philippe, Dubertret, Caroline, Schwan, Raymund, Aubin, Valerie, Roux, Paul, Polosan, Mircea, Samalin, Ludovic, Haffen, Emmanuel, Olié, Emilie, Godin, Ophelia, Etain, B., Olié, E., Leboyer, M., Haffen, E., Llorca, P. M., Barteau, V., Bensalem, S., Godin, O., Laouamri, H., Souryis, K., Hotier, S., Pelletier, A., Wuillaume, L., Bourdin, E., Bellivier, F., Etain, B., Hennion, V., Marlinge, E., Lebard, P., Aouizerate, B., Desage, A., Gard, S., Jutant, A., Mbailara, K., Minois, I., Zanouy, L., Abettan, C., Bardin, L., Cazals, A., Deffinis, B., Ducasse, D., Gachet, M., Henrion, A., Martinerie, E., Molière, F., Noisette, B., Olié, E., Tarquini, G., Cermolacce, M., Correard, N., Consoloni, J. L., Groppi, F., Lescalier, L., Montant, J., Rebattu, M., Viglianese, N., Cohen, R., Gross, G., Schwan, R., Schwitzer, T., Wajsbrot‐Elgrabli, O., Bougerol, T., Fredembach, B., Denoual, Q., Bertrand, A., Pouchon, A., Polosan, M., Bonny, G., Brehon, L, Durand, L, Feuga, V, Galliot, A. M., Kayser, N., Passerieux, C., Roux, P., Aubin, V., Cussac, I., Dupont, M. A, Loftus, J., Medecin, I., Dubertret, C., Mazer, N., Dubertret, C., Laurent, Pauline, Beal, C., Blanc, O., Bonnet, T., Lacelle, D., Llorca, P. M., Mennetrier, M., Samalin, L., Vayssié, M.

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Correction: Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD) by Pinto E Vairo, Filippo, Kemppainen, Jennifer L, Vitek, Carolyn R Rohrer, Whalen, Denise A, Kolbert, Kayla J, Sikkink, Kaitlin J, Kroc, Sarah A, Kruisselbrink, Teresa, Shupe, Gabrielle F, Knudson, Alyssa K, Burke, Elizabeth M, Loftus, Elle C, Bandel, Lorelei A, Prochnow, Carri A, Mulvihill, Lindsay A, Thomas, Brittany, Gable, Dale M, Graddy, Courtney B, Garzon, Giovanna G Moreno, Ekpoh, Idara U, Porquera, Eva M Carmona, Fervenza, Fernando C, Hogan, Marie C, El Ters, Mireille, Warrington, Kenneth J, Davis, 3rd, John M, Koster, Matthew J, Orandi, Amir B, Basiaga, Matthew L, Vella, Adrian, Kumar, Seema, Creo, Ana L, Lteif, Aida N, Pittock, Siobhan T, Tebben, Peter J, Abate, Ejigayehu G, Joshi, Avni Y, Ristagno, Elizabeth H, Patnaik, Mrinal S, Schimmenti, Lisa A, Dhamija, Radhika, Sabrowsky, Sonia M, Wierenga, Klaas J, Keddis, Mira T, Samadder, Niloy Jewel J, Presutti, Richard J, Robinson, Steven I, Stephens, Michael C, Roberts, Lewis R, Faubion, Jr, William A, Driscoll, Sherilyn W, Wong-Kisiel, Lily C, Selcen, Duygu, Flanagan, Eoin P, Ramanan, Vijay K, Jackson, Lauren M, Mauermann, Michelle L, Ortega, Victor E, Anderson, Sarah A, Aoudia, Stacy L, Klee, Eric W, McAllister, Tammy M, Lazaridis, Konstantinos N

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Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD) by Pinto E Vairo, Filippo, Kemppainen, Jennifer L, Vitek, Carolyn R Rohrer, Whalen, Denise A, Kolbert, Kayla J, Sikkink, Kaitlin J, Kroc, Sarah A, Kruisselbrink, Teresa, Shupe, Gabrielle F, Knudson, Alyssa K, Burke, Elizabeth M, Loftus, Elle C, Bandel, Lorelei A, Prochnow, Carri A, Mulvihill, Lindsay A, Thomas, Brittany, Gable, Dale M, Graddy, Courtney B, Garzon, Giovanna G Moreno, Ekpoh, Idara U, Porquera, Eva M Carmona, Fervenza, Fernando C, Hogan, Marie C, El Ters, Mireille, Warrington, Kenneth J, Davis, 3rd, John M, Koster, Matthew J, Orandi, Amir B, Basiaga, Matthew L, Vella, Adrian, Kumar, Seema, Creo, Ana L, Lteif, Aida N, Pittock, Siobhan T, Tebben, Peter J, Abate, Ejigayehu G, Joshi, Avni Y, Ristagno, Elizabeth H, Patnaik, Mrinal S, Schimmenti, Lisa A, Dhamija, Radhika, Sabrowsky, Sonia M, Wierenga, Klaas J, Keddis, Mira T, Samadder, Niloy Jewel J, Presutti, Richard J, Robinson, Steven I, Stephens, Michael C, Roberts, Lewis R, Faubion, Jr, William A, Driscoll, Sherilyn W, Wong-Kisiel, Lily C, Selcen, Duygu, Flanagan, Eoin P, Ramanan, Vijay K, Jackson, Lauren M, Mauermann, Michelle L, Ortega, Victor E, Anderson, Sarah A, Aoudia, Stacy L, Klee, Eric W, McAllister, Tammy M, Lazaridis, Konstantinos N

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Niemann-Pick C1 Disease Gene: Homology to Mediators of Cholesterol Homeostasis by Carstea, Eugene D., Morris, Jill A., Coleman, Katherine G., Loftus, Stacie K., Zhang, Dana, Cummings, Christiano, Gu, Jessie, Rosenfeld, Melissa A., Pavan, William J., Krizman, David B., Nagle, James, Polymeropoulos, Mihail H., Sturley, Stephen L., Ioannou, Yiannis A., Higgins, Maureen E., Comly, Marcella, Cooney, Adele, Brown, Anthony, Kaneski, Christine R., Blanchette-Mackie, E. Joan, Dwyer, Nancy K., Neufeld, Edward B., Chang, Ta-Yuan, Liscum, Laura, Strauss, Jerome F., Ohno, Kousaku, Zeigler, Marsha, Carmi, Rivka, Sokol, Jacob, Markie, David, O'Neill, Raymond R., van Diggelen, O. P., Elleder, Milan, Patterson, Marc C., Brady, Roscoe O., Vanier, Marie T., Pentchev, Peter G., Tagle, Danilo A.

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