Որոնման արդյունքները - Tarjinder Singh

Հստակեցնել արդյունքները
  1. 1
    Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

    Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia ‌ Tarjinder Singh, Benjamin M. Neale, Mark J. Daly

    Հրապարակվել է 2020
    Ստացեք ամբողջական տեքստը Ստացեք ամբողջական տեքստը
    Pré-impressão
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  2. 2
    Hippo Signaling Regulates Differentiation and Maintenance in the Exocrine Pancreas

    Hippo Signaling Regulates Differentiation and Maintenance in the Exocrine Pancreas ‌ Tao Gao, Dawang Zhou, Chenghua Yang, Tarjinder Singh, Alfredo Penzo‐Méndez, Ravikanth Maddipati, Alexandros Tzatsos, Nabeel Bardeesy, Joseph Avruch, Ben Z. Stanger

    Հրապարակվել է 2013
    Ստացեք ամբողջական տեքստը
    Artigo
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  3. 3
    Genome Wide Association Study of Fetal Hemoglobin in Sickle Cell Anemia in Tanzania

    Genome Wide Association Study of Fetal Hemoglobin in Sickle Cell Anemia in Tanzania ‌ Siana Nkya, Tarjinder Singh, Helen Rooks, Josephine Mgaya, Harvest Mariki, Deogratius Soka, Bruno P. Mmbando, Evarist Msaki, I. Kolder, Swee Lay Thein, Stephan Menzel, Sharon E. Cox, Julie Makani, Jeffrey C. Barrett

    Հրապարակվել է 2014
    Ստացեք ամբողջական տեքստը Ստացեք ամբողջական տեքստը
    Artigo
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  4. 4
    The genetic architecture and evolution of the human skeletal form

    The genetic architecture and evolution of the human skeletal form ‌ Eucharist Kun, Emily Javan, Olivia S. Smith, Faris F. Gulamali, Javier de la Fuente, Brianna I. Flynn, Kushal Vajrala, Zoe Trutner, Prakash Jayakumar, Elliot M. Tucker‐Drob, Mashaal Sohail, Tarjinder Singh, Vagheesh M. Narasimhan

    Հրապարակվել է 2023
    Ստացեք ամբողջական տեքստը
    Artigo
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  5. 5
    Pdx1 Maintains β Cell Identity and Function by Repressing an α Cell Program

    Pdx1 Maintains β Cell Identity and Function by Repressing an α Cell Program ‌ Tao Gao, Brian D. McKenna, Changhong Li, Maximilian Reichert, James Nguyen, Tarjinder Singh, Chenghua Yang, Archana Pannikar, Nicolai M. Doliba, Tingting Zhang, Doris A. Stoffers, Helena Edlund, Franz Matschinsky, Roland Stein, Ben Z. Stanger

    Հրապարակվել է 2014
    Ստացեք ամբողջական տեքստը Ստացեք ամբողջական տեքստը
    Artigo
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  6. 6
    Contribution of retrotransposition to developmental disorders

    Contribution of retrotransposition to developmental disorders ‌ Eugene J. Gardner, Elena Prigmore, Giuseppe Gallone, Petr Danecek, Kaitlin E. Samocha, Juliet Handsaker, Sebastian S. Gerety, Holly Ironfield, Patrick Short, Alejandro Sifrim, Tarjinder Singh, Kate Chandler, Emma Clement, Katherine Lachlan, Katrina Prescott, Elisabeth Rosser, David Fitzpatrick, Helen V. Firth, Matthew E. Hurles

    Հրապարակվել է 2019
    Ստացեք ամբողջական տեքստը Ստացեք ամբողջական տեքստը
    Artigo
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  7. 7
    Complement C1q-dependent excitatory and inhibitory synapse elimination by astrocytes and microglia in Alzheimer’s disease mouse models

    Complement C1q-dependent excitatory and inhibitory synapse elimination by astrocytes and microglia in Alzheimer’s disease mouse models ‌ Borislav Dejanovic, Tiffany Wu, Ming‐Chi Tsai, David Graykowski, Vineela Gandham, Christopher M. Rose, Corey E. Bakalarski, Hai Ngu, Yuanyuan Wang, Shristi Pandey, Mitchell G. Rezzonico, Brad A. Friedman, Rose Edmonds, Ann De Mazière, Raphael Rakosi-Schmidt, Tarjinder Singh, Judith Klumperman, Oded Foreman, Michael Chang, Luke Xie, Morgan Sheng, Jesse E. Hanson

    Հրապարակվել է 2022
    Ստացեք ամբողջական տեքստը Ստացեք ամբողջական տեքստը
    Artigo
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  8. 8
    Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

    Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants ‌ F. Kyle Satterstrom, Raymond K. Walters, Tarjinder Singh, Emilie M. Wigdor, Francesco Lescai, Ditte Demontis, Jack A. Kosmicki, Jakob Grove, Christine Stevens, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Duncan S. Palmer, Julian Maller, Merete Nordentoft, Ole Mors, Elise Robinson, David M. Hougaard, Thomas Werge, Preben Bo Mortensen, Benjamin M. Neale, Anders D. Børglum, Mark J. Daly

    Հրապարակվել է 2019
    Ստացեք ամբողջական տեքստը
    Artigo
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  9. 9
    The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability

    The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability ‌ Tarjinder Singh, James Walters, Mandy Johnstone, David Curtis, Jaana Suvisaari, Minna Torniainen, Elliott Rees, Conrad Iyegbe, Douglas Blackwood, Andrew M. McIntosh, George Kirov, Daniel H. Geschwind, Robin Murray, Marta Di Forti, Elvira Bramon, Michael J. Gandal, Christina M. Hultman, Pamela Sklar, Aarno Palotie, Patrick F. Sullivan, Michael O’Donovan, Michael J. Owen, Jeffrey C. Barrett

    Հրապարակվել է 2017
    Ստացեք ամբողջական տեքստը
    Revisão
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  10. 10
    Exome sequencing in schizophrenia-affected parent–offspring trios reveals risk conferred by protein-coding de novo mutations

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

    Հրապարակվել է 2020
    Ստացեք ամբողջական տեքստը
    Artigo
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  11. 11
    De novo variants in neurodevelopmental disorders with epilepsy

    De novo variants in neurodevelopmental disorders with epilepsy ‌ Henrike Heyne, Tarjinder Singh, Hannah Stamberger, Rami Abou Jamra, Hande Çağlayan, Dana Craiu, Peter De Jonghe, Renzo Guerrini, Katherine L. Helbig, Bobby P.C. Koeleman, Jack A. Kosmicki, Tarja Linnankivi, Patrick May, Hiltrud Muhle, Rikke S. Møller, Bernd A. Neubauer, Aarno Palotie, Manuela Pendziwiat, Pasquale Striano, Sha Tang, Sitao Wu, Annapurna Poduri, Yvonne G. Weber, Sarah Weckhuysen, Sanjay M. Sisodiya, Mark J. Daly, Ingo Helbig, Dennis Lal, Johannes R. Lemke

    Հրապարակվել է 2018
    Ստացեք ամբողջական տեքստը
    Artigo
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  12. 12
    Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia

    Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia ‌ Duncan S. Palmer, Daniel P. Howrigan, Sinéad B. Chapman, Rolf Adolfsson, Nicholas Bass, Douglas Blackwood, Marco P. Boks, Chia‐Yen Chen, Claire Churchhouse, Aiden Corvin, Nicholas Craddock, David Curtis, Arianna Di Florio, Faith Dickerson, Nelson B. Freimer, Fernando S. Goes, Xiaoming Jia, Ian Jones, Lisa Jones, Lina Jönsson, René S. Kahn, Mikael Landén, Adam E. Locke, Andrew M. McIntosh, Andrew McQuillin, Derek W. Morris, Michael O’Donovan, Roel A. Ophoff, Michael J. Owen, Nancy L. Pedersen, Daniëlle Posthuma, Andreas Reif, Neil Risch, Catherine Schaefer, Laura J. Scott, Tarjinder Singh, Jordan W. Smoller, Matthew Solomonson, David St Clair, Eli A. Stahl, Annabel Vreeker, James Walters, Weiqing Wang, Nicholas A. Watts, Robert H. Yolken, Peter P. Zandi, Benjamin M. Neale

    Հրապարակվել է 2022
    Ստացեք ամբողջական տեքստը
    Revisão
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  13. 13
    The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia

    The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia ‌ Ralda Nehme, Olli Pietiläinen, Mykyta Artomov, Matthew Tegtmeyer, Vera Valakh, Leevi Lehtonen, Christina Bell, Tarjinder Singh, Aditi Trehan, J. L. Sherwood, Danielle K. Manning, Emily Peirent, Rhea Malik, Ellen J. Guss, Derek Hawes, Amanda Beccard, Anne M. Bara, Dane Z. Hazelbaker, Emanuela Zuccaro, Giulio Genovese, Alexander A. Loboda, Anna Neumann, Christina Lilliehöök, Outi Kuismin, Eija Hämäläinen, Mitja Kurki, Christina M. Hultman, Anna K. Kähler, João A. Paulo, Andrea Ganna, Jon M. Madison, Bruce M. Cohen, Donna L. McPhie, Rolf Adolfsson, Roy H. Perlis, Ricardo E. Dolmetsch, Samouil L. Farhi, Steven A. McCarroll, Steven E. Hyman, Ben Neale, Lindy E. Barrett, J. Wade Harper, Aarno Palotie, Mark J. Daly, Kevin Eggan

    Հրապարակվել է 2022
    Ստացեք ամբողջական տեքստը Ստացեք ամբողջական տեքստը
    Artigo
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  14. 14
    Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

    Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders ‌ Tarjinder Singh, Mitja Kurki, David Curtis, Shaun Purcell, Lucy Crooks, Jeremy F. McRae, Jaana Suvisaari, Himanshu Chheda, Douglas Blackwood, Gerome Breen, Olli Pietiläinen, Sebastian S. Gerety, Muhammad Ayub, Moira Blyth, Trevor Cole, David Collier, Eve L. Coomber, Nick Craddock, Mark J. Daly, John Danesh, Marta Di Forti, Alison Foster, Nelson B. Freimer, Daniel H. Geschwind, Mandy Johnstone, Shelagh Joss, George Kirov, Jarmo Körkkö, Outi Kuismin, Peter Holmans, Christina M. Hultman, Conrad Iyegbe, Jouko Lönnqvist, Minna Männikkö, Steve McCarroll, Peter McGuffin, Andrew M. McIntosh, Andrew McQuillin, Jukka S. Moilanen, Carmel Moore, Robin Murray, Ruth Newbury‐Ecob, Willem H. Ouwehand, Tiina Paunio, Elena Prigmore, Elliott Rees, David J. Roberts, Jennifer Sambrook, Pamela Sklar, David St Clair, Juha Veijola, James Walters, Hywel Williams, Patrick F. Sullivan, Matthew E. Hurles, Michael O’Donovan, Aarno Palotie, Michael J. Owen, Jeffrey C. Barrett

    Հրապարակվել է 2016
    Ստացեք ամբողջական տեքստը
    Artigo
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  15. 15
    Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing

    Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing ‌ Alejandro Sifrim, Marc‐Phillip Hitz, Anna Wilsdon, Jeroen Breckpot, Saeed H. Al Turki, Bernard Thienpont, Jeremy F. McRae, Tomas Fitzgerald, Tarjinder Singh, G. Jawahar Swaminathan, Elena Prigmore, Diana Rajan, Hashim Abdul‐Khaliq, Siddharth Banka, Ulrike Bauer, Jamie Bentham, Felix Berger, Shoumo Bhattacharya, Frances Bu’Lock, Natalie Canham, Irina-Gabriela Colgiu, Catherine Cosgrove, Helen Cox, Ingo Daehnert, Allan Daly, John Danesh, Alan Fryer, Marc Gewillig, Emma Hobson, Kirstin Hoff, Tessa Homfray, Anne-Karin Kahlert, Ami Ketley, Hans-Heiner Kramer, Katherine Lachlan, Anne Katrin Lampe, Jacoba Louw, Ashok Kumar Manickara, Dorin Manase, Karen McCarthy, Kay Metcalfe, Carmel Moore, Ruth Newbury‐Ecob, Seham Osman Babiker Omer, Willem H. Ouwehand, Soo‐Mi Park, Michael Parker, Thomas Pickardt, Martin Pollard, Leema Robert, David J. Roberts, Jennifer Sambrook, Kerry Setchfield, Brigitte Stiller, Chris Thornborough, Okan Toka, Hugh Watkins, Denise Williams, Michael Wright, Seema Mital, Piers E.F. Daubeney, Bernard Keavney, Judith Goodship, Riyadh Mahdi Abu-Sulaiman, Sabine Klaassen, Caroline F. Wright, Helen V. Firth, Jeffrey C. Barrett, Koenraad Devriendt, David Fitzpatrick, J. David Brook, Matthew E. Hurles

    Հրապարակվել է 2016
    Ստացեք ամբողջական տեքստը
    Artigo
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  16. 16
    The impact of rare protein coding genetic variation on adult cognitive function

    The impact of rare protein coding genetic variation on adult cognitive function ‌ Chia‐Yen Chen, Ruoyu Tian, Tian Ge, Max Lam, Gabriela Sánchez-Andrade, Tarjinder Singh, Lea Urpa, Jimmy Z. Liu, Mark Sanderson, Christine Rowley, Holly Ironfield, Terry Fang, Aija Kyttälä, Amanda Elliott, Anders Kämpe, André Sourander, Annamari Tuulio‐Henriksson, Anssi Solismaa, Antti Tanskanen, Ari Ahola‐Olli, Arto Mustonen, Arttu Honkasalo, Asko Wegelius, Atiqul Haq Mazumder, Auli Toivola, Benjamin M. Neale, Elina Hietala, Elmo Saarentaus, Erik Cederlöf, Erkki Isometsä, Heidi Taipale, Imre Västrik, Jaana Suvisaari, Jari Tiihonen, Jarmo Hietala, Johan Ahti, Jonne Lintunen, Jouko Lönnqvist, Juha Veijola, Julia Moghadampour, Jussi Niemi-Pynttäri, Kaisla Lahdensuo, Katja Häkkinen, Katriina Hakakari, Kimmo Suokas, Marjo Taivalantti, Markku Lähteenvuo, Martta Kerkelä, Minna Torniainen‐Holm, Nina Lindberg, Noora Ristiluoma, Olli Kampman, Olli Pietiläinen, Risto Kajanne, Sari Lång-Tonteri, Solja Niemelä, Steven E. Hyman, Susanna Rask, Teemu Männynsalo, Tiina Paunio, Tuomas Jukuri, Tuomo Kiiskinen, Tuula Kieseppä, Ville Mäkipelto, Willehard Haaki, Zuzanna Misiewicz, Mitja Kurki, Jarmo Körkkö, Jukka S. Moilanen, Outi Kuismin, Mark J. Daly, Aarno Palotie, Ellen Tsai, Hailiang Huang, Matthew E. Hurles, Sebastian S. Gerety, Todd Lencz, Heiko Runz

    Հրապարակվել է 2023
    Ստացեք ամբողջական տեքստը Ստացեք ամբողջական տեքստը
    Artigo
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  17. 17
    Synaptic, transcriptional and chromatin genes disrupted in autism

    Synaptic, transcriptional and chromatin genes disrupted in autism ‌ Silvia De Rubeis, Xin He, Arthur P. Goldberg, Christopher S. Poultney, Kaitlin E. Samocha, A. Ercüment Çiçek, Yan Kou, Li Liu, Menachem Fromer, Susan L. Walker, Tarjinder Singh, Lambertus Klei, Jack A. Kosmicki, Shih‐Chen Fu, Branko Aleksić, Monica Biscaldi, Patrick Bolton, Jessica M. Brownfeld, Jinlu Cai, Nicholas G. Campbell, Ángel Carracedo, Maria H. Chahrour, Andreas G. Chiocchetti, Hilary Coon, Emily L. Crawford, Lucy Crooks, Sarah Curran, Géraldine Dawson, Eftichia Duketis, Bridget A. Fernandez, Louise Gallagher, Evan Geller, Stephen J. Guter, R. Sean Hill, Iuliana Ionita‐Laza, Patricia González, Helena Kilpinen, Sabine M. Klauck, Alexander Kolevzon, Irene Lee, Jing Lei, Terho Lehtimäki, Chiao‐Feng Lin, Avi Ma’ayan, Christian R. Marshall, Alison McInnes, Benjamin M. Neale, Michael J. Owen, Norio Ozaki, Mara Parellada, Jeremy Parr, Shaun Purcell, Kaija Puura, Deepthi Rajagopalan, Karola Rehnström, Abraham Reichenberg, Aniko Sabo, Michael Max Sachse, Stephan Sanders, Chad Schafer, Martin Schulte‐Rüther, David Skuse, Christine Stevens, Peter Szatmari, Kristiina Tammimies, Otto Valladares, Annette Voran, Li‐San Wang, Lauren A. Weiss, A. Jeremy Willsey, Timothy W. Yu, Ryan K. C. Yuen, Edwin H. Cook, Christine M. Freitag, Michael Gill, Christina M. Hultman, Thomas Lehner, Aarno Palotie, Gerard D. Schellenberg, Pamela Sklar, Matthew W. State, James S. Sutcliffe, Christopher A. Walsh, Stephen W. Scherer, Michael E. Zwick, Jeffrey C. Barrett, David J. Cutler, Kathryn Roeder, Bernie Devlin, Mark J. Daly, Joseph D. Buxbaum

    Հրապարակվել է 2014
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    Artigo
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  18. 18
    Prevalence, phenotype and architecture of developmental disorders caused by <i>de novo</i> mutation: The Deciphering Developmental Disorders Study

    Prevalence, phenotype and architecture of developmental disorders caused by <i>de novo</i> mutation: The Deciphering Developmental Disorders Study ‌ Jeremy F. McRae, Stephen Clayton, Tomas Fitzgerald, Joanna Kaplanis, Elena Prigmore, Diana Rajan, Alejandro Sifrim, Stuart Aitken, Nadia Akawi, Mohsan Alvi, Kirsty Ambridge, Daniel M. Barrett, Tanya Bayzetinova, Philip Jones, Wendy D. Jones, Daniel A. King, Netravathi Krishnappa, Laura E. Mason, Tarjinder Singh, Adrian R. Tivey, Munaza Ahmed, Uruj Anjum, Hayley Archer, Ruth Armstrong, Jana Awada, Meena Balasubramanian, Siddharth Banka, Diana Baralle, Angela Barnicoat, Paul Batstone, David Baty, Chris Bennett, Jonathan Berg, Birgitta Bernhard, A. Paul Bevan, Maria Bitner‐Glindzicz, Edward Blair, Moira Blyth, David Bohanna, Louise Bourdon, David Bourn, Lisa Bradley, Angela Brady, Simon Brent, Carole Brewer, Kate Brunstrom, David J. Bunyan, John Burn, Natalie Canham, Bruce Castle, Kate Chandler, Elena Chatzimichali, Deirdre Cilliers, Angus Clarke, Susan Clasper, Jill Clayton‐Smith, Virginia Clowes, Andrea Coates, Trevor Cole, Irina Colgiu, Amanda Collins, Morag N. Collinson, Fiona Connell, Nicola Cooper, Helen Cox, Lara Cresswell, Gareth Cross, Yanick J. Crow, Mariella D’Alessandro, Tabib Dabir, Rosemarie Davidson, Sally Davies, Dylan H. de Vries, John Dean, Charu Deshpande, Gemma Devlin, Abhijit Dixit, Angus Dobbie, Alan Donaldson, Dian Donnai, Deirdre Donnelly, Carina Donnelly, Angela Douglas, Sofia Douzgou, Alexis E. Duncan, Jacqueline Eason, Sian Ellard, Ian O. Ellis, Frances Elmslie, Karenza Evans, Sarah Everest, Tina Fendick, Richard Fisher, Frances Flinter, Nicola Foulds, AndrewW Fry, Alan Fryer, Carol Gardiner, Lorraine Gaunt, Neeti Ghali

    Հրապարակվել է 2016
    Ստացեք ամբողջական տեքստը
    Pré-impressão
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  19. 19
    Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders

    Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders ‌ Víctor Faúndes, William G. Newman, Laura Bernardini, Natalie Canham, Jill Clayton‐Smith, Bruno Dallapiccola, Sally Davies, Michelle Demos, Amy Goldman, Harinder Gill, Rachel Horton, Bronwyn Kerr, Dhavendra Kumar, Anna Lehman, Shane McKee, Jenny Morton, Michael Parker, Julia Rankin, Lisa Robertson, I. Karen Temple, Siddharth Banka, Shelin Adam, Christèle du Souich, Alison M. Elliott, Anna Lehman, Jill Mwenifumbo, Tanya N. Nelson, Clara van Karnebeek, Jan M. Friedman, Jeremy F. McRae, Stephen Clayton, Tomas Fitzgerald, Joanna Kaplanis, Elena Prigmore, Diana Rajan, Alejandro Sifrim, Stuart Aitken, Nadia Akawi, Mohsan Alvi, Kirsty Ambridge, Daniel M. Barrett, Tanya Bayzetinova, Philip Jones, Wendy D. Jones, Daniel King, Netravathi Krishnappa, Laura E. Mason, Tarjinder Singh, Adrian R. Tivey, Munaza Ahmed, Uruj Anjum, Hayley Archer, Ruth Armstrong, Jana Awada, Meena Balasubramanian, Siddharth Banka, Diana Baralle, Angela Barnicoat, Paul Batstone, David Baty, Chris Bennett, Jonathan Berg, Birgitta Bernhard, A. Paul Bevan, Maria Bitner‐Glindzicz, Edward Blair, Moira Blyth, David Bohanna, Louise Bourdon, David Bourn, Lisa Bradley, Angela F. Brady, Simon Brent, Carole Brewer, Kate Brunstrom, David J. Bunyan, John Burn, Natalie Canham, Bruce Castle, Kate Chandler, Elena Chatzimichali, Deirdre Cilliers, Angus Clarke, Susan Clasper, Jill Clayton‐Smith, Virginia Clowes, Andrea Coates, Trevor Cole, Irina Colgiu, Amanda Collins, Morag N. Collinson, Fiona Connell, Nicola Cooper, Helen Cox, Lara Cresswell, Gareth Cross, Yanick J. Crow, Mariella D’Alessandro, Tabib Dabir, Rosemarie Davidson

    Հրապարակվել է 2017
    Ստացեք ամբողջական տեքստը
    Artigo
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  20. 20
    CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

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    Ստացեք ամբողջական տեքստը Ստացեք ամբողջական տեքստը
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