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	1.	Detecting autozygosity through runs of homozygosity: a comparison of three autozygosity detection algorithms. [electronic resource] by Howrigan, Daniel P Simonson, Matthew A Keller, Matthew C Producer: 20120111 In: BMC genomics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia. [electronic resource] by Bergen, Sarah E Ploner, Alexander Howrigan, Daniel O'Donovan, Michael C Smoller, Jordan W Sullivan, Patrick F Sebat, Jonathan Neale, Benjamin Kendler, Kenneth S Producer: 20191023 In: The American journal of psychiatry vol. 176 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mutational load analysis of unrelated individuals. [electronic resource] by Howrigan, Daniel P Simonson, Matthew A Kamens, Helen M Stephens, Sarah H Wills, Amanda G Ehringer, Marissa A Keller, Matthew C McQueen, Matthew B Producer: 20121002 In: BMC proceedings vol. 5 Suppl 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Runs of homozygosity implicate autozygosity as a schizophrenia risk factor. [electronic resource] by Keller, Matthew C Simonson, Matthew A Ripke, Stephan Neale, Ben M Gejman, Pablo V Howrigan, Daniel P Lee, Sang Hong Lencz, Todd Levinson, Douglas F Sullivan, Patrick F Producer: 20120926 In: PLoS genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Spatiotemporal profile of postsynaptic interactomes integrates components of complex brain disorders. [electronic resource] by Li, Jing Zhang, Wangshu Yang, Hui Howrigan, Daniel P Wilkinson, Brent Souaiaia, Tade Evgrafov, Oleg V Genovese, Giulio Clementel, Veronica A Tudor, Jennifer C Abel, Ted Knowles, James A Neale, Benjamin M Wang, Kai Sun, Fengzhu Coba, Marcelo P Producer: 20170905 In: Nature neuroscience vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples. [electronic resource] by Kosmicki, Jack A Samocha, Kaitlin E Howrigan, Daniel P Sanders, Stephan J Slowikowski, Kamil Lek, Monkol Karczewski, Konrad J Cutler, David J Devlin, Bernie Roeder, Kathryn Buxbaum, Joseph D Neale, Benjamin M MacArthur, Daniel G Wall, Dennis P Robinson, Elise B Daly, Mark J Producer: 20170905 In: Nature genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Genome-Wide Association Study of Behavioral Disinhibition in a Selected Adolescent Sample. [electronic resource] by Derringer, Jaime Corley, Robin P Haberstick, Brett C Young, Susan E Demmitt, Brittany A Howrigan, Daniel P Kirkpatrick, Robert M Iacono, William G McGue, Matt Keller, Matthew C Brown, Sandra Tapert, Susan Hopfer, Christian J Stallings, Michael C Crowley, Thomas J Rhee, Soo Hyun Krauter, Ken Hewitt, John K McQueen, Matthew B Producer: 20160307 In: Behavior genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects. [electronic resource] by Regier, Allison A Farjoun, Yossi Larson, David E Krasheninina, Olga Kang, Hyun Min Howrigan, Daniel P Chen, Bo-Juen Kher, Manisha Banks, Eric Ames, Darren C English, Adam C Li, Heng Xing, Jinchuan Zhang, Yeting Matise, Tara Abecasis, Goncalo R Salerno, Will Zody, Michael C Neale, Benjamin M Hall, Ira M Producer: 20190122 In: Nature communications vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Paternal-age-related de novo mutations and risk for five disorders. [electronic resource] by Taylor, Jacob L Debost, Jean-Christophe P G Morton, Sarah U Wigdor, Emilie M Heyne, Henrike O Lal, Dennis Howrigan, Daniel P Bloemendal, Alex Larsen, Janne T Kosmicki, Jack A Weiner, Daniel J Homsy, Jason Seidman, Jonathan G Seidman, Christine E Agerbo, Esben McGrath, John J Mortensen, Preben Bo Petersen, Liselotte Daly, Mark J Robinson, Elise B Producer: 20191021 In: Nature communications vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations. [electronic resource] by 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 Producer: 20200413 In: Nature neuroscience vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies. [electronic resource] by Pérez-Palma, Eduardo Helbig, Ingo Klein, Karl Martin Anttila, Verneri Horn, Heiko Reinthaler, Eva Maria Gormley, Padhraig Ganna, Andrea Byrnes, Andrea Pernhorst, Katharina Toliat, Mohammad R Saarentaus, Elmo Howrigan, Daniel P Hoffman, Per Miquel, Juan Francisco De Ferrari, Giancarlo V Nürnberg, Peter Lerche, Holger Zimprich, Fritz Neubauer, Bern A Becker, Albert J Rosenow, Felix Perucca, Emilio Zara, Federico Weber, Yvonne G Lal, Dennis Producer: 20180430 In: Journal of medical genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Ultra-rare disruptive and damaging mutations influence educational attainment in the general population. [electronic resource] by Ganna, Andrea Genovese, Giulio Howrigan, Daniel P Byrnes, Andrea Kurki, Mitja Zekavat, Seyedeh M Whelan, Christopher W Kals, Mart Nivard, Michel G Bloemendal, Alex Bloom, Jonathan M Goldstein, Jacqueline I Poterba, Timothy Seed, Cotton Handsaker, Robert E Natarajan, Pradeep Mägi, Reedik Gage, Diane Robinson, Elise B Metspalu, Andres Salomaa, Veikko Suvisaari, Jaana Purcell, Shaun M Sklar, Pamela Kathiresan, Sekar Daly, Mark J McCarroll, Steven A Sullivan, Patrick F Palotie, Aarno Esko, Tõnu Hultman, Christina Neale, Benjamin M Producer: 20170905 In: Nature neuroscience vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study. [electronic resource] by Johnson, Emma C Bjelland, Douglas W Howrigan, Daniel P Abdellaoui, Abdel Breen, Gerome Borglum, Anders Cichon, Sven Degenhardt, Franziska Forstner, Andreas J Frank, Josef Genovese, Giulio Heilmann-Heimbach, Stefanie Herms, Stefan Hoffman, Per Maier, Wolfgang Mattheisen, Manuel Morris, Derek Mowry, Bryan Müller-Mhysok, Betram Neale, Benjamin Nenadic, Igor Nöthen, Markus M O'Dushlaine, Colm Rietschel, Marcella Ruderfer, Douglas M Rujescu, Dan Schulze, Thomas G Simonson, Matthew A Stahl, Eli Strohmaier, Jana Witt, Stephanie H Sullivan, Patrick F Keller, Matthew C Producer: 20170428 In: PLoS genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Integrating evolutionary and regulatory information with a multispecies approach implicates genes and pathways in obsessive-compulsive disorder. [electronic resource] by Noh, Hyun Ji Tang, Ruqi Flannick, Jason O'Dushlaine, Colm Swofford, Ross Howrigan, Daniel Genereux, Diane P Johnson, Jeremy van Grootheest, Gerard Grünblatt, Edna Andersson, Erik Djurfeldt, Diana R Patel, Paresh D Koltookian, Michele M Hultman, Christina Pato, Michele T Pato, Carlos N Rasmussen, Steven A Jenike, Michael A Hanna, Gregory L Stewart, S Evelyn Knowles, James A Ruhrmann, Stephan Grabe, Hans-Jörgen Wagner, Michael Rück, Christian Mathews, Carol A Walitza, Susanne Cath, Daniëlle C Feng, Guoping Karlsson, Elinor K Lindblad-Toh, Kerstin Producer: 20180123 In: Nature communications vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein. [electronic resource] by Farhan, Sali M K Howrigan, Daniel P Abbott, Liam E Klim, Joseph R Topp, Simon D Byrnes, Andrea E Churchhouse, Claire Phatnani, Hemali Smith, Bradley N Rampersaud, Evadnie Wu, Gang Wuu, Joanne Shatunov, Aleksey Iacoangeli, Alfredo Al Khleifat, Ahmad Mordes, Daniel A Ghosh, Sulagna Eggan, Kevin Rademakers, Rosa McCauley, Jacob L Schüle, Rebecca Züchner, Stephan Benatar, Michael Taylor, J Paul Nalls, Michael Gotkine, Marc Shaw, Pamela J Morrison, Karen E Al-Chalabi, Ammar Traynor, Bryan Shaw, Christopher E Goldstein, David B Harms, Matthew B Daly, Mark J Neale, Benjamin M Producer: 20200131 In: Nature neuroscience vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Publisher Correction: Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein. [electronic resource] by Farhan, Sali M K Howrigan, Daniel P Abbott, Liam E Klim, Joseph R Topp, Simon D Byrnes, Andrea E Churchhouse, Claire Phatnani, Hemali Smith, Bradley N Rampersaud, Evadnie Wu, Gang Wuu, Joanne Shatunov, Aleksey Iacoangeli, Alfredo Khleifat, Ahmad Al Mordes, Daniel A Ghosh, Sulagna Eggan, Kevin Rademakers, Rosa McCauley, Jacob L Schüle, Rebecca Züchner, Stephan Benatar, Michael Taylor, J Paul Nalls, Michael Gotkine, Marc Shaw, Pamela J Morrison, Karen E Al-Chalabi, Ammar Traynor, Bryan Shaw, Christopher E Goldstein, David B Harms, Matthew B Daly, Mark J Neale, Benjamin M Publication details: Nature neuroscience Feb 2020 In: Nature neuroscience vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	SynGO: An Evidence-Based, Expert-Curated Knowledge Base for the Synapse. [electronic resource] by Koopmans, Frank van Nierop, Pim Andres-Alonso, Maria Byrnes, Andrea Cijsouw, Tony Coba, Marcelo P Cornelisse, L Niels Farrell, Ryan J Goldschmidt, Hana L Howrigan, Daniel P Hussain, Natasha K Imig, Cordelia de Jong, Arthur P H Jung, Hwajin Kohansalnodehi, Mahdokht Kramarz, Barbara Lipstein, Noa Lovering, Ruth C MacGillavry, Harold Mariano, Vittoria Mi, Huaiyu Ninov, Momchil Osumi-Sutherland, David Pielot, Rainer Smalla, Karl-Heinz Tang, Haiming Tashman, Katherine Toonen, Ruud F G Verpelli, Chiara Reig-Viader, Rita Watanabe, Kyoko van Weering, Jan Achsel, Tilmann Ashrafi, Ghazaleh Asi, Nimra Brown, Tyler C De Camilli, Pietro Feuermann, Marc Foulger, Rebecca E Gaudet, Pascale Joglekar, Anoushka Kanellopoulos, Alexandros Malenka, Robert Nicoll, Roger A Pulido, Camila de Juan-Sanz, Jaime Sheng, Morgan Südhof, Thomas C Tilgner, Hagen U Bagni, Claudia Bayés, Àlex Biederer, Thomas Brose, Nils Chua, John Jia En Dieterich, Daniela C Gundelfinger, Eckart D Hoogenraad, Casper Huganir, Richard L Jahn, Reinhard Kaeser, Pascal S Kim, Eunjoon Kreutz, Michael R McPherson, Peter S Neale, Ben M O'Connor, Vincent Posthuma, Danielle Ryan, Timothy A Sala, Carlo Feng, Guoping Hyman, Steven E Thomas, Paul D Smit, August B Verhage, Matthijs Producer: 20191021 In: Neuron vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Analysis of protein-coding genetic variation in 60,706 humans. [electronic resource] by 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 Producer: 20160913 In: Nature vol. 536 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Identification of common genetic risk variants for autism spectrum disorder. [electronic resource] by Grove, Jakob Ripke, Stephan Als, Thomas D Mattheisen, Manuel Walters, Raymond K Won, Hyejung Pallesen, Jonatan Agerbo, Esben Andreassen, Ole A Anney, Richard Awashti, Swapnil Belliveau, Rich Bettella, Francesco Buxbaum, Joseph D Bybjerg-Grauholm, Jonas Bækvad-Hansen, Marie Cerrato, Felecia Chambert, Kimberly Christensen, Jane H Churchhouse, Claire Dellenvall, Karin Demontis, Ditte De Rubeis, Silvia Devlin, Bernie Djurovic, Srdjan Dumont, Ashley L Goldstein, Jacqueline I Hansen, Christine S Hauberg, Mads Engel Hollegaard, Mads V Hope, Sigrun Howrigan, Daniel P Huang, Hailiang Hultman, Christina M Klei, Lambertus Maller, Julian Martin, Joanna Martin, Alicia R Moran, Jennifer L Nyegaard, Mette Nærland, Terje Palmer, Duncan S Palotie, Aarno Pedersen, Carsten Bøcker Pedersen, Marianne Giørtz dPoterba, Timothy Poulsen, Jesper Buchhave Pourcain, Beate St Qvist, Per Rehnström, Karola Reichenberg, Abraham Reichert, Jennifer Robinson, Elise B Roeder, Kathryn Roussos, Panos Saemundsen, Evald Sandin, Sven Satterstrom, F Kyle Davey Smith, George Stefansson, Hreinn Steinberg, Stacy Stevens, Christine R Sullivan, Patrick F Turley, Patrick Walters, G Bragi Xu, Xinyi Stefansson, Kari Geschwind, Daniel H Nordentoft, Merete Hougaard, David M Werge, Thomas Mors, Ole Mortensen, Preben Bo Neale, Benjamin M Daly, Mark J Børglum, Anders D Producer: 20190424 In: Nature genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. [electronic resource] by Demontis, Ditte Walters, Raymond K Martin, Joanna Mattheisen, Manuel Als, Thomas D Agerbo, Esben Baldursson, Gísli Belliveau, Rich Bybjerg-Grauholm, Jonas Bækvad-Hansen, Marie Cerrato, Felecia Chambert, Kimberly Churchhouse, Claire Dumont, Ashley Eriksson, Nicholas Gandal, Michael Goldstein, Jacqueline I Grasby, Katrina L Grove, Jakob Gudmundsson, Olafur O Hansen, Christine S Hauberg, Mads Engel Hollegaard, Mads V Howrigan, Daniel P Huang, Hailiang Maller, Julian B Martin, Alicia R Martin, Nicholas G Moran, Jennifer Pallesen, Jonatan Palmer, Duncan S Pedersen, Carsten Bøcker Pedersen, Marianne Giørtz Poterba, Timothy Poulsen, Jesper Buchhave Ripke, Stephan Robinson, Elise B Satterstrom, F Kyle Stefansson, Hreinn Stevens, Christine Turley, Patrick Walters, G Bragi Won, Hyejung Wright, Margaret J Andreassen, Ole A Asherson, Philip Burton, Christie L Boomsma, Dorret I Cormand, Bru Dalsgaard, Søren Franke, Barbara Gelernter, Joel Geschwind, Daniel Hakonarson, Hakon Haavik, Jan Kranzler, Henry R Kuntsi, Jonna Langley, Kate Lesch, Klaus-Peter Middeldorp, Christel Reif, Andreas Rohde, Luis Augusto Roussos, Panos Schachar, Russell Sklar, Pamela Sonuga-Barke, Edmund J S Sullivan, Patrick F Thapar, Anita Tung, Joyce Y Waldman, Irwin D Medland, Sarah E Stefansson, Kari Nordentoft, Merete Hougaard, David M Werge, Thomas Mors, Ole Mortensen, Preben Bo Daly, Mark J Faraone, Stephen V Børglum, Anders D Neale, Benjamin M Producer: 20190424 In: Nature genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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