A 28-fold increase in secretory protein synthesis is associated with DNA puff activity in the salivary gland of Bradysia hygida (Diptera, Sciaridae) by de-Almeida J.C.

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Cor de solo, formas do fósforo e adsorção de fosfatos em Latossolos desenvolvidos de basalto do extremo-sul do Brasil by Almeida J. A., Torrent J., Barrón V.

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Avaliação de três áreas de solo construído após mineração de carvão a céu aberto em Lauro Müller, Santa Catarina by Campos M. L., Almeida J. A., Souza L. S.

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Anaesthesia for myocardial revascularisation in a patient with portal hypertension. by Khanvelkar K, Date S, Almeida J, Basu A, Jagtap R

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The ENIGMA Consortium: Large-scale collaborative analyses of neuroimaging and genetic data by Thompson, P, Stein, J, Medland, SE, Hibar, D, Vasquez, A, Vasquez, A, Renteria, M, Toro, R, Toro, R, Toro, R, Jahanshad, N, Schumann, G, Franke, B, Franke, B, Wright, M, Martin, N, Agartz, I, Agartz, I, Alda, M, Alhusaini, S, Alhusaini, S, Almasy, L, Almeida, J, Almeida, J, Almeida, J

Interatrial septum dissection, severe aortic stenosis, and paravalvular mitral regurgitation: A rare combination and their hemodynamic interrelationship by Di Silvestre M, Muñoz‐Rodríguez R, Tindaya‐Herraiz A, Bosa‐Ojeda F, Barragan‐Acea A, Bonilla A, Lacalzada‐Almeida J

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P16-17. Antigen sensitivity is a major determinant of CD8+ T-cell polyfunctionality and HIV suppressive activity by Saez-Cirion A, Autran B, Douek D, Pancino G, Larsen M, Moris A, Shin S, Papagno L, Price D, Sauce D, Almeida J, Appay V

Compression of the right coronary artery by an aortic pseudoaneurysm after infective endocarditis: an unusual case of myocardial ischemia by Lacalzada-Almeida J, De la Rosa-Hernández A, Izquierdo-Gómez MM, García-Niebla J, Hernández-Betancor I, Bonilla-Arjona JA, Barragán-Acea A, Laynez-Cerdeña I

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Transoral tongue base mucosectomy for the identification of the primary site in the work-up of cancers of unknown origin: Systematic review and meta-analysis by Farooq, S, Khandavilli, S, Dretzke, J, Moore, D, Nankivell, P, Sharma, N, Almeida, J, Winter, S, Simon, C, Paleri, V, De, M, Siddiq, S, Holsinger, C, Ferris, R, Mehanna, H

“The Nobodies”: unidentified dead bodies—a global health crisis requiring urgent attention by Suwalowska, H, Ali, J, Rangel de Almeida, J, Fonseca, SA, Heathfield, LJ, Keyes, CA, Lukande, R, Martin, LJ, Reid, KM, Vaswani, V, Wasti, H, Wilson, RO, Parker, M, Kingori, P

Mammals, Serra da Concórdia, state of Rio de Janeiro, Brazil. by Bergallo, H. G., Esbérard, C. E. L., Pereira, B. C., Albuquerque, H, G., Raíces, D. S. L., Almeida, J., Attias, N., Costa, L. M., Enrici, M. C., Jordão-Nogueira, T., Pessôa, F. S., Modesto, T. C.

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Connexin43 promotes exocytosis of damaged lysosomes through actin remodelling by Domingues, N, Catarino, S, Cristóvão, B, Rodrigues, L, Carvalho, FA, Sarmento, MJ, Zuzarte, M, Almeida, J, Ribeiro-Rodrigues, T, Correia-Rodrigues, Â, Fernandes, F, Rodrigues-Santos, P, Aasen, T, Santos, NC, Korolchuk, VI, Gonçalves, T, Milosevic, I, Raimundo, N, Girão, H

A genome-wide scan for common alleles affecting risk for autism. by Anney, R, Klei, L, Pinto, D, Regan, R, Conroy, J, Magalhaes, T, Correia, C, Abrahams, B, Sykes, N, Pagnamenta, A, Almeida, J, Bacchelli, E, Bailey, A, Baird, G, Battaglia, A, Berney, T, Bolshakova, N, Bölte, S, Bolton, P, Bourgeron, T, Brennan, S, Brian, J, Carson, A, Casallo, G, Casey, J

Functional impact of global rare copy number variation in autism spectrum disorders. by Pinto, D, Pagnamenta, A, Klei, L, Anney, R, Merico, D, Regan, R, Conroy, J, Magalhaes, T, Correia, C, Abrahams, B, Almeida, J, Bacchelli, E, Bader, G, Bailey, A, Baird, G, Battaglia, A, Berney, T, Bolshakova, N, Bölte, S, Bolton, P, Bourgeron, T, Brennan, S, Brian, J, Bryson, SE, Carson, A

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. by Casey, J, Magalhaes, T, Conroy, J, Regan, R, Shah, N, Anney, R, Shields, D, Abrahams, B, Almeida, J, Bacchelli, E, Bailey, A, Baird, G, Battaglia, A, Berney, T, Bolshakova, N, Bolton, P, Bourgeron, T, Brennan, S, Cali, P, Correia, C, Corsello, C, Coutanche, M, Dawson, G, de Jonge, M, Delorme, R

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. by Casey, J, Magalhaes, T, Conroy, J, Regan, R, Shah, N, Anney, R, Shields, D, Abrahams, B, Almeida, J, Bacchelli, E, Bailey, A, Baird, G, Battaglia, A, Berney, T, Bolshakova, N, Bolton, P, Bourgeron, T, Brennan, S, Cali, P, Correia, C, Corsello, C, Coutanche, M, Dawson, G, de Jonge, M, Delorme, R

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. by Thompson, P, Stein, J, Medland, SE, Hibar, D, Vasquez, A, Renteria, M, Toro, R, Jahanshad, N, Schumann, G, Franke, B, Wright, M, Martin, N, Agartz, I, Alda, M, Alhusaini, S, Almasy, L, Almeida, J, Alpert, K, Andreasen, N, Andreassen, O, Apostolova, L, Appel, K, Armstrong, N, Aribisala, B, Bastin, M

Variation in wood density across South American tropical forests by Sullivan, MJP, Phillips, OL, Galbraith, D, Almeida, E, de Oliveira, EA, Almeida, J, Dávila, EÁ, Alves, LF, Andrade, A, Aragão, L, Araujo-Murakami, A, Arets, E, Arroyo, L, Cruz, OAM, Baccaro, F, Baker, TR, Banki, O, Baraloto, C, Barlow, J, Barroso, J, Berenguer, E, Blanc, L, Blundo, C, Bonal, D, Huasco, WH, Malhi, Y

Impact of primary kidney disease on the effects of empagliflozin in patients with chronic kidney disease: secondary analyses of the EMPA-KIDNEY trial by Staplin, N, Mayne, MJ, Abat, S, Abd Rahman, R, Abdul Cader, R, Abdul Hafidz, MI, Abdul Wahab, MZ, Abdullah, NK, Abdul-Samad, T, Abe, M, Abraham, N, Acheampong, S, Achiri, P, Acosta, JA, Adeleke, A, Adell, V, Adewuyi-Dalton, R, Adnan, N, Africano, A, Agharazii, M, Aguilar, F, Aguilera, A, Ahmad, M, Ahmad, MK, Ahmad, NA, Ahmad, NH, Ahmad, NI, Ahmad Miswan, N, Ahmad Rosdi, H, Ahmed, I, Ahmed, S, Aiello, J, Aitken, A, AitSadi, R, Aker, S, Akimoto, S, Akinfolarin, A, Akram, S, Alberici, F, Albert, C, Aldrich, L, Alegata, M, Alexander, L, Alfaress, S, Alhadj Ali, M, Ali, A, Alicic, R, Aliu, A, Almaraz, R, Almasarwah, R, Almeida, J, Aloisi, A

Individual common variants exert weak effects on the risk for autism spectrum disorderspi. by Anney, R, Klei, L, Pinto, D, Almeida, J, Bacchelli, E, Baird, G, Bolshakova, N, Bölte, S, Bolton, P, Bourgeron, T, Brennan, S, Brian, J, Casey, J, Conroy, J, Correia, C, Corsello, C, Crawford, E, de Jonge, M, Delorme, R, Duketis, E, Duque, F, Estes, A, Farrar, P, Fernandez, B, Folstein, SE, Fombonne, E, Gilbert, J, Gillberg, C, Glessner, J, Green, A, Green, J, Guter, S, Heron, E, Holt, R, Howe, J, Hughes, G, Hus, V, Igliozzi, R, Jacob, S, Kenny, G, Kim, C, Kolevzon, A, Kustanovich, V, Lajonchere, C, Lamb, J, Law-Smith, M, Leboyer, M, Le Couteur, A, Leventhal, B, Liu, X, Lombard, F, Lord, C, Lotspeich, L, Lund, S, Magalhaes, T, Mantoulan, C, McDougle, C, Melhem, N, Merikangas, A, Minshew, N, Mirza, G, Munson, J, Noakes, C, Nygren, G, Papanikolaou, K, Pagnamenta, A, Parrini, B, Paton, T, Pickles, A, Posey, D, Poustka, F, Ragoussis, I, Regan, R, Roberts, W, Roeder, K, Roge, B, Rutter, M, Schlitt, S, Shah, N, Sheffield, VC, Soorya, L, Sousa, I, Stoppioni, V, Sykes, N, Tancredi, R, Thompson, A, Thomson, S, Tryfon, A, Tsiantis, J, Van Engeland, H, Vincent, J, Volkmar, F, Vorstman, J, Wallace, S, Wing, K, Wittemeyer, K, Wood, S, Zurawiecki, D, Zwaigenbaum, L, Bailey, A, Battaglia, A, Cantor, R, Coon, H, Cuccaro, M, Dawson, G, Ennis, S, Freitag, C, Geschwind, D, Haines, J, Klauck, S, McMahon, WM, Maestrini, E, Miller, J, Monaco, A, Nelson, S, Nurnberger, J, Oliveira, G, Oliveira, G, Parr, JR, Pericak-Vance, M, Piven, J, Schellenberg, G, Scherer, S, Vicente, A, Wassink, T, Wijsman, E, Betancur, C, Buxbaum, J, Cook, E, Gallagher, L, Gill, M, Hallmayer, J, Paterson, A, Sutcliffe, J, Szatmari, P, Vieland, V, Hakonarson, H, Devlin, B