Evaluation of flecainide acetate in rapid atrial fibrillation complicating wolff‐parkinson‐white syndrome von Kappenberger, L. J., Fromer, M. A., Shenasa, M., Gloor, H. O.

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Efficacy of amiodarone in the wolff-parkinson-white syndrome with rapid ventricular response via accessory pathway during atrial fibrillation von Kappenberger, Lukas J., Fromer, Martin A., Steinbrunn, Walter, Shenasa, Mohammad

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Indications and Limitations of Class I Drugs in Atrial Fibrillation von FROMER, MARTIN A.

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Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence von Genovese, Giulio, Kähler, Anna K, Handsaker, Robert E, Lindberg, Johan, Rose, Samuel A, Bakhoum, Samuel F, Chambert, Kimberly, Mick, Eran, Neale, Benjamin M, Fromer, Menachem, Purcell, Shaun M, Svantesson, Oscar, Landén, Mikael, Höglund, Martin, Lehmann, Sören, Gabriel, Stacey B, Moran, Jennifer L, Lander, Eric S, Sullivan, Patrick F, Sklar, Pamela, Grönberg, Henrik, Hultman, Christina M, McCarroll, Steven A

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Prevention of Anaphylaxis: The Role of the Epinephrine Auto-Injector von Fromer, Leonard, MD

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Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia von Genovese, Giulio, Fromer, Menachem, Stahl, Eli A, Ruderfer, Douglas M, Chambert, Kimberly, Landén, Mikael, Moran, Jennifer L, Purcell, Shaun M, Sklar, Pamela, Sullivan, Patrick F, Hultman, Christina M, McCarroll, Steven A

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Discovery and Statistical Genotyping of Copy-Number Variation from Whole-Exome Sequencing Depth von FROMER, Menachem, MORAN, Jennifer L, KIROV, George, SULLIVAN, Patrick F, HULTMAN, Christina M, SKLAR, Pamela, PURCELL, Shaun M, CHAMBERT, Kimberly, BANKS, Eric, BERGEN, Sarah E, RUDERFER, DouglasM, HANDSAKER, Robert E, MCCARROLL, Steven A, O'DONOVAN, Michael C, OWEN, Michael J

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Air-Stable All-Inorganic Nanocrystal Solar Cells Processed from Solution von Gur, Ilan, Fromer, Neil A, Geier, Michael L, Alivisatos, A. Paul

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Copy number variation in schizophrenia in Sweden von Szatkiewicz, J P, O'Dushlaine, C, Chen, G, Chambert, K, Moran, J L, Neale, B M, Fromer, M, Ruderfer, D, Akterin, S, Bergen, S E, Kähler, A, Magnusson, P K E, Kim, Y, Crowley, J J, Rees, E, Kirov, G, O'Donovan, M C, Owen, M J, Walters, J, Scolnick, E, Sklar, P, Purcell, S, Hultman, C M, McCarroll, S A, Sullivan, P F

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Functional analysis of rare variants found in schizophrenia implicates a critical role for GIT1–PAK3 signaling in neuroplasticity von Kim, M J, Biag, J, Fass, D M, Lewis, M C, Zhang, Q, Fleishman, M, Gangwar, S P, Machius, M, Fromer, M, Purcell, S M, McCarroll, S A, Rudenko, G, Premont, R T, Scolnick, E M, Haggarty, S J

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Exome sequencing in schizophrenia-affected parent–offspring trios reveals risk conferred by protein-coding de novo mutations von Howrigan, Daniel P., Rose, Samuel A., Samocha, Kaitlin E., Fromer, Menachem, Cerrato, Felecia, Chen, Wei J., Churchhouse, Claire, Chambert, Kimberly, Chandler, Sharon D., Daly, Mark J., Dumont, Ashley, Genovese, Giulio, Hwu, Hai-Gwo, Laird, Nan, Kosmicki, Jack A., Moran, Jennifer L., Roe, Cheryl, Singh, Tarjinder, Wang, Shi-Heng, Faraone, Stephen V., Glatt, Stephen J., McCarroll, Steven A., Tsuang, Ming, Neale, Benjamin M.

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A Role for Noncoding Variation in Schizophrenia von Roussos, Panos, Mitchell, Amanda C., Voloudakis, Georgios, Fullard, John F., Pothula, Venu M., Tsang, Jonathan, Stahl, Eli A., Georgakopoulos, Anastasios, Ruderfer, Douglas M., Charney, Alexander, Okada, Yukinori, Siminovitch, Katherine A., Worthington, Jane, Padyukov, Leonid, Klareskog, Lars, Gregersen, Peter K., Plenge, Robert M., Raychaudhuri, Soumya, Fromer, Menachem, Purcell, Shaun M., Brennand, Kristen J., Robakis, Nikolaos K., Schadt, Eric E., Akbarian, Schahram, Sklar, Pamela

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De novo mutations in schizophrenia implicate synaptic networks von Fromer, Menachem, Pocklington, Andrew J., Kavanagh, David H., Williams, Hywel J., Dwyer, Sarah, Gormley, Padhraig, Georgieva, Lyudmila, Rees, Elliott, Palta, Priit, Ruderfer, Douglas M., Carrera, Noa, Humphreys, Isla, Johnson, Jessica S., Roussos, Panos, Barker, Douglas D., Banks, Eric, Milanova, Vihra, Grant, Seth G., Hannon, Eilis, Rose, Samuel A., Chambert, Kimberly, Mahajan, Milind, Scolnick, Edward M., Moran, Jennifer L., Kirov, George, Palotie, Aarno, McCarroll, Steven A., Holmans, Peter, Sklar, Pamela, Owen, Michael J., Purcell, Shaun M., O’Donovan, Michael C.

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A polygenic burden of rare disruptive mutations in schizophrenia von Purcell, Shaun M., Moran, Jennifer L., Fromer, Menachem, Ruderfer, Douglas, Solovieff, Nadia, Roussos, Panos, O’Dushlaine, Colm, Chambert, Kimberly, Bergen, Sarah E., Kähler, Anna, Duncan, Laramie, Stahl, Eli, Genovese, Giulio, Fernández, Esperanza, Collins, Mark O., Komiyama, Noboru H., Choudhary, Jyoti S., Magnusson, Patrik K. E., Banks, Eric, Shakir, Khalid, Garimella, Kiran, Fennell, Tim, DePristo, Mark, Grant, Seth G. N., Haggarty, Stephen J., Gabriel, Stacey, Scolnick, Edward M., Lander, Eric S., Hultman, Christina M., Sullivan, Patrick F., McCarroll, Steven A., Sklar, Pamela

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zCall: a rare variant caller for array-based genotyping von GOLDSTEIN, Jacqueline I, CRENSHAW, Andrew, SCHIZOPHRENIA CONSORTIUM, Swedish, SEQUENCING CONSORTIUM, Arra Autism, SKLAR, Pamela, HULTMAN, Christina M, PURCELL, Shaun, MCCARROLL, Steven A, SULLIVAN, Patrick F, DALY, Mark J, NEALE, Benjamin M, CAREY, Jason, GRANT, George B, MAGUIRE, Jared, FROMER, Menachem, O'DUSHLAINE, Colm, MORAN, Jennifer L, CHAMBERT, Kimberly, STEVENS, Christine

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Patterns of genic intolerance of rare copy number variation in 59,898 human exomes von Ruderfer, Douglas M, Hamamsy, Tymor, Lek, Monkol, Karczewski, Konrad J, Kavanagh, David, Samocha, Kaitlin E, Daly, Mark J, MacArthur, Daniel G, Fromer, Menachem, Purcell, Shaun M

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Using XHMM Software to Detect Copy Number Variation in Whole‐Exome Sequencing Data von Fromer, Menachem, Purcell, Shaun M.

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Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders von Nguyen, Hoang T, Bryois, Julien, Kim, April, Dobbyn, Amanda, Huckins, Laura M, Munoz-Manchado, Ana B, Ruderfer, Douglas M, Genovese, Giulio, Fromer, Menachem, Xu, Xinyi, Pinto, Dalila, Linnarsson, Sten, Verhage, Matthijs, Smit, August B, Hjerling-Leffler, Jens, Buxbaum, Joseph D, Hultman, Christina, Sklar, Pamela, Purcell, Shaun M, Lage, Kasper, He, Xin, Sullivan, Patrick F, Stahl, Eli A

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Analysis of protein-coding genetic variation in 60,706 humans von Lek, Monkol, Karczewski, Konrad J., Minikel, Eric V., Samocha, Kaitlin E., Banks, Eric, Fennell, Timothy, O’Donnell-Luria, Anne H., Ware, James S., Hill, Andrew J., Cummings, Beryl B., Tukiainen, Taru, Birnbaum, Daniel P., Kosmicki, Jack A., Duncan, Laramie E., Estrada, Karol, Zhao, Fengmei, Zou, James, Pierce-Hoffman, Emma, Berghout, Joanne, Cooper, David N., Deflaux, Nicole, DePristo, Mark, Do, Ron, Flannick, Jason, Fromer, Menachem, Gauthier, Laura, Goldstein, Jackie, Gupta, Namrata, Howrigan, Daniel, Kiezun, Adam, Kurki, Mitja I., Moonshine, Ami Levy, Natarajan, Pradeep, Orozco, Lorena, Peloso, Gina M., Poplin, Ryan, Rivas, Manuel A., Ruano-Rubio, Valentin, Rose, Samuel A., Ruderfer, Douglas M., Shakir, Khalid, Stenson, Peter D., Stevens, Christine, Thomas, Brett P., Tiao, Grace, Tusie-Luna, Maria T., Weisburd, Ben, Won, Hong-Hee, Yu, Dongmei, Altshuler, David M., Ardissino, Diego, Boehnke, Michael, Danesh, John, Donnelly, Stacey, Elosua, Roberto, Florez, Jose C., Gabriel, Stacey B., Getz, Gad, Glatt, Stephen J., Hultman, Christina M., Kathiresan, Sekar, Laakso, Markku, McCarroll, Steven, McCarthy, Mark I., McGovern, Dermot, McPherson, Ruth, Neale, Benjamin M., Palotie, Aarno, Purcell, Shaun M., Saleheen, Danish, Scharf, Jeremiah M., Sklar, Pamela, Sullivan, Patrick F., Tuomilehto, Jaakko, Tsuang, Ming T., Watkins, Hugh C., Wilson, James G., Daly, Mark J., MacArthur, Daniel G.

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Characterization of Single Gene Copy Number Variants in Schizophrenia von Szatkiewicz, Jin P., Fromer, Menachem, Nonneman, Randal J., Ancalade, NaEshia, Johnson, Jessica S., Stahl, Eli A., Rees, Elliott, Bergen, Sarah E., Hultman, Christina M., Kirov, George, O’Donovan, Michael, Owen, Michael, Holmans, Peter, Sklar, Pamela, Sullivan, Patrick F., Purcell, Shaun M., Crowley, James J., Ruderfer, Douglas M.

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