खोज परिणाम - Daniel A. King
- प्रदर्शित 1 - 19 परिणाम 19
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Nutritional Aspects of Chronic Obstructive Pulmonary Disease द्वारा Daniel A. King, Francis Cordova, Steven M. Scharf
प्रकाशित 2008Revisão -
2
A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders द्वारा Daniel A. King, Tomas Fitzgerald, Ray Miller, Natalie Canham, Jill Clayton‐Smith, Diana Johnson, Sahar Mansour, Fiona Stewart, Pradeep Vasudevan, Matthew E. Hurles
प्रकाशित 2013Artigo -
3
Detection of structural mosaicism from targeted and whole-genome sequencing data द्वारा Daniel A. King, Alejandro Sifrim, Tomas Fitzgerald, Raheleh Rahbari, Emma Hobson, Tessa Homfray, Sahar Mansour, Sarju Mehta, Mohammed Shehla, Susan Tomkins, Pradeep Vasudevan, Matthew E. Hurles
प्रकाशित 2017Artigo -
4
Atypical Antigen Recognition Mode of a Shark Immunoglobulin New Antigen Receptor (IgNAR) Variable Domain Characterized by Humanization and Structural Analysis द्वारा Oleg Kovalenko, Andrea Olland, Nicole Piche‐Nicholas, Adarsh Godbole, Daniel A. King, Kristine Svenson, Valérie Calabro, Mischa Müller, Caroline J. Barelle, W.S. Somers, Davinder Gill, Lidia Mosyak, Lioudmila Tchistiakova
प्रकाशित 2013Artigo -
5
Absence of Heterozygosity Due to Template Switching during Replicative Rearrangements द्वारा Claudia M.B. Carvalho, Rolph Pfundt, Daniel A. King, Sarah Lindsay, Luciana W. Zuccherato, Merryn Macville, Pengfei Liu, Diana Johnson, Paweł Stankiewicz, Chester Brown, Chad A. Shaw, Matthew E. Hurles, Grzegorz Ira, P. J. Hastings, Han G. Brunner, James R. Lupski
प्रकाशित 2015Artigo -
6
Single cell analysis reveals distinct immune landscapes in transplant and primary sarcomas that determine response or resistance to immunotherapy द्वारा Amy J. Wisdom, Yvonne M. Mowery, Cierra S. Hong, Jonathon E. Himes, Barzin Y. Nabet, Xiaodi Qin, Dadong Zhang, Lan Chen, Hélène Fradin, Rutulkumar Patel, Alex M. Bassil, Eric S. Muise, Daniel A. King, Eric S. Xu, David Carpenter, Collin Kent, Kimberly S. Smythe, Nerissa T. Williams, Lixia Luo, Yan Ma, Ash A. Alizadeh, Kouros Owzar, Maximilian Diehn, Todd Bradley, David G. Kirsch
प्रकाशित 2020Artigo -
7
Pancreatic Cancer Patient-derived Organoids Can Predict Response to Neoadjuvant Chemotherapy द्वारा Lyudmyla Demyan, Amber N. Habowski, Dennis Plenker, Daniel A. King, Oliver Standring, Caitlin Tsang, Luce St. Surin, Arvind Rishi, James M. Crawford, Jeff Boyd, Shamsher A. Pasha, Hardik Patel, Zachary Galluzzo, Christine N. Metz, Peter K. Gregersen, Sharon S. Fox, Cristina Valente, Sonya Abadali, Steffi Matadial-Ragoo, Danielle K. DePeralta, Gary B. Deutsch, Joseph M. Herman, Mark A. Talamini, David A. Tuveson, Matthew J. Weiss
प्रकाशित 2022Artigo -
8
A High Through-put Platform for Recombinant Antibodies to Folded Proteins द्वारा Michael Hornsby, Marcin Paduch, Shane Miersch, Annika Sääf, Tet Matsuguchi, Brian H. Lee, Karolina Wypisniak, Allison K. Doak, Daniel A. King, Svitlana Usatyuk, Kimberly J. Perry, Vince Lu, William D. Thomas, Judy Luke, Jay S. Goodman, Robert J. Hoey, Darson Lai, Carly Griffin, Zhijian Li, Franco J. Vizeacoumar, Debbie Dong, Elliot Campbell, Stephen K. Anderson, Nan Zhong, S. Gräslund, Shohei Koide, Jason Moffat, Sachdev S. Sidhu, Anthony A. Kossiakoff, James A. Wells
प्रकाशित 2015Artigo -
9
Mosaic structural variation in children with developmental disorders द्वारा Daniel A. King, Wendy D. Jones, Yanick J. Crow, Anna F. Dominiczak, N Foster, Tom R. Gaunt, Jade Harris, Stephen Hellens, Tessa Homfray, Josie Innes, Elizabeth A. Jones, Shelagh Joss, Abhijit Kulkarni, Sahar Mansour, Andrew D. Morris, Michael Parker, David J. Porteous, Hashem A. Shihab, Blair H. Smith, Katrina Tatton‐Brown, John Tolmie, Maciej Trzaskowski, Pradeep Vasudevan, Emma Wakeling, Michael Wright, Robert Plomin, Nicholas J. Timpson, Matthew E. Hurles
प्रकाशित 2015Artigo -
10
Immunotherapy and Targeted Therapy for Advanced Gastroesophageal Cancer: ASCO Guideline द्वारा Manish A. Shah, Erin B. Kennedy, Ashley E. Alarcon-Rozas, Thierry Alcindor, Angela N. Bartley, Aubrey Belk Malowany, Nishin A. Bhadkamkar, Dana C. Deighton, Yelena Y. Janjigian, Asha Karippot, Uqba Khan, Daniel A. King, Kelsey Klute, Jill Lacy, James J. Lee, Rutika Mehta, Sarbajit Mukherjee, Arun Nagarajan, Haeseong Park, Anwaar Saeed, Thomas J. Semrad, Kohei Shitara, Elizabeth Smyth, Nataliya V. Uboha, Melani Vincelli, Zev A. Wainberg, Lakshmi Rajdev
प्रकाशित 2023Revisão -
11
Pan-UK Biobank GWAS improves discovery, analysis of genetic architecture, and resolution into ancestry-enriched effects द्वारा Konrad J. Karczewski, Rahul Gupta, Masahiro Kanai, Wenhan Lu, Kristin Tsuo, Ying Wang, Raymond K. Walters, Patrick Turley, Shawneequa Callier, Nirav N. Shah, Nikolas Baya, Duncan S. Palmer, Jacqueline I. Goldstein, Gopal Sarma, Matthew Solomonson, Nathan Cheng, Sam Bryant, Claire Churchhouse, Caroline Cusick, Timothy Poterba, John Compitello, Daniel A. King, Wei Zhou, Cotton Seed, Hilary K. Finucane, Mark J. Daly, Benjamin M. Neale, Elizabeth G. Atkinson, Alicia R. Martin
प्रकाशित 2024Pré-impressão -
12
Inferring gene expression from cell-free DNA fragmentation profiles द्वारा Mohammad Shahrokh Esfahani, Emily G. Hamilton, Mahya Mehrmohamadi, Barzin Y. Nabet, Stefan Alig, Daniel A. King, Chloé B. Steen, Charles Macaulay, André Schultz, Monica Nesselbush, Joanne Soo, Joseph G. Schroers‐Martin, Binbin Chen, Michael S. Binkley, Henning Stehr, Jacob J. Chabon, Brian J. Sworder, Angela BY Hui, Matthew J. Frank, Everett J. Moding, Chih Long Liu, Aaron M. Newman, James M. Isbell, Charles M. Rudin, Bob T. Li, David M. Kurtz, Maximilian Diehn, Ash A. Alizadeh
प्रकाशित 2022Artigo -
13
Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data द्वारा Caroline F. Wright, Tomas Fitzgerald, Wendy D. Jones, Stephen Clayton, Jeremy F. McRae, Margriet van Kogelenberg, Daniel A. King, Kirsty Ambridge, Daniel M. Barrett, Tanya Bayzetinova, A. Paul Bevan, Eugene Bragin, Eleni Anthippi Chatzimichali, Susan Gribble, Philip Jones, Netravathi Krishnappa, Laura E. Mason, Ray Miller, Katherine I. Morley, Vijaya Parthiban, Elena Prigmore, Diana Rajan, Alejandro Sifrim, G. Jawahar Swaminathan, Adrian R. Tivey, Anna Middleton, Michael Parker, Nigel P. Carter, Jeffrey C. Barrett, Matthew E. Hurles, David Fitzpatrick, Helen V. Firth
प्रकाशित 2014Artigo -
14
Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families द्वारा Nadia Akawi, Jeremy F. McRae, Morad Ansari, Meena Balasubramanian, Moira Blyth, Angela F. Brady, Stephen Clayton, Trevor Cole, Charu Deshpande, Tomas Fitzgerald, Nicola Foulds, Richard Francis, George C. Gabriel, Sebastian S. Gerety, Judith Goodship, Emma Hobson, Wendy D. Jones, Shelagh Joss, Daniel A. King, Nikolai Klena, Ajith Kumar, Melissa Lees, Chris Lelliott, Jenny Lord, Dominic McMullan, Mary O’Regan, Deborah Osio, Virginia Piombo, Elena Prigmore, Diana Rajan, Elisabeth Rosser, Alejandro Sifrim, Audrey Smith, G. Jawahar Swaminathan, Peter D. Turnpenny, James W. Whitworth, Caroline F. Wright, Helen V. Firth, Jeffrey C. Barrett, Cecilia Lo, David Fitzpatrick, Matthew E. Hurles
प्रकाशित 2015Artigo -
15
Distinct Hodgkin lymphoma subtypes defined by noninvasive genomic profiling द्वारा Stefan Alig, Mohammad Shahrokh Esfahani, Andrea Garofalo, Michael Y. Li, Cédric Rossi, Tim Flerlage, Jamie E. Flerlage, Ragini Adams, Michael S. Binkley, Navika Shukla, Michael C. Jin, Mari Olsen, Adèle Telenius, Jurik Mutter, Joseph G. Schroers‐Martin, Brian J. Sworder, Shinya Rai, Daniel A. King, André Schultz, Jan Bögeholz, Shengqin Su, Karan R. Kathuria, Chih Long Liu, Xiaoman Kang, Maya J. Strohband, Deanna Langfitt, Kristine Faye Pobre-Piza, Sherri L. Surman, Feng Tian, Valeria Spina, Thomas Tousseyn, Lieselot Buedts, Richard T. Hoppe, Yasodha Natkunam, Luc‐Matthieu Fornecker, Sharon M. Castellino, Ranjana H. Advani, Davide Rossi, Ryan C. Lynch, Hervé Ghesquières, Olivier Casasnovas, David M. Kurtz, Lianna J. Marks, Michael P. Link, Marc André, Peter Vandenberghe, Christian Steidl, Maximilian Diehn, Ash A. Alizadeh
प्रकाशित 2023Artigo -
16
The Project Baseline Health Study: a step towards a broader mission to map human health द्वारा Kristine Arges, Themistocles L. Assimes, Vikram S. Bajaj, Suresh Balu, Mustafa R. Bashir, Laura M. Beskow, Rosalia Blanco, Robert M. Califf, Paul Campbell, Lawrence Carin, Victoria Christian, Scott W. Cousins, Millie Das, Marie Dockery, Pamela S. Douglas, Ashley Dunham, Julie Eckstrand, Dominik Fleischmann, Emily Ford, Elizabeth Fraulo, John French, Sanjiv S. Gambhir, Geoffrey S. Ginsburg, Robert C. Green, François Haddad, Adrian F. Hernandez, John Hernandez, Erich Huang, Glenn J. Jaffe, Daniel A. King, Lynne Koweek, Curtis P. Langlotz, Yaping Joyce Liao, Kenneth W. Mahaffey, Kelly Marcom, William J. Marks, David J. Maron, Reid McCabe, Shannon J. McCall, Rebecca McCue, Jessica L. Mega, David P. Miller, Lawrence H. Muhlbaier, Rajan Munshi, L. Kristin Newby, Ezra Pak-Harvey, Bray Patrick‐Lake, Michael J. Pencina, Eric D. Peterson, Fátima Rodríguez, Scarlet Shore, Svati H. Shah, Steven Shipes, George W. Sledge, Susie Spielman, Ryan Spitler, Terry Schaack, Geeta K. Swamy, Martin J. Willemink, Charlene A. Wong
प्रकाशित 2020Revisão -
17
Prevalence, phenotype and architecture of developmental disorders caused by <i>de novo</i> mutation: The Deciphering Developmental Disorders Study द्वारा 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
प्रकाशित 2016Pré-impressão -
18
Not all <i>SCN1A</i> epileptic encephalopathies are Dravet syndrome द्वारा Lynette G. Sadleir, Emily Mountier, Deepak Gill, Suzanne L. Davis, Charuta Joshi, Catherine DeVile, Manju A. Kurian, Simone Mandelstam, Elaine Wirrell, Katherine Nickels, Hema Murali, Gemma L. Carvill, Candace T. Myers, Heather C. Mefford, Ingrid E. Scheffer, A. Paul Bevan, Abhijit Dixit, Abigail Pridham, Adrian R. Tivey, Ajoy Sarkar, Alan Donaldson, Alan Fryer, Alejandro Sifrim, Alex Henderson, Alex Magee, Alexis E. Duncan, Alison Kraus, Alison Male, Alison Ross, Amanda Collins, Anand Saggar, Andrea Coates, Andrea H. Németh, Andrew E. Fry, Andrew Green, A. Jackson, Andrew Norman, Angela Barnicoat, Angela Brady, Angela Douglas, Angus Clarke, Angus Dobbie, Ann Selby, Anna Middleton, Anne Lampe, A Seller, Annie Procter, Karenza Evans, Anthony Vandersteen, Astrid Weber, Audrey Smith, Audrey Torokwa, Beckie Kaemba, Becky Treacy, Beiyuan Fu, Ben Hutton, Birgitta Bernhard, Bronwyn Kerr, Bruce Castle, Carina Donnelly, Carol Gardiner, Clare L. Scott, Carole Brewer, Caroline F. Wright, Caroline Langman, Caroline Mackie Ogilvie, Caroline Pottinger, Carolyn Tysoe, Cat Taylor, Catherine McWilliam, Charles Shaw‐Smith, Charu Deshpande, Cheryl Longman, Cheryl Sequeira, Chirag Patel, Chris Bennett, Chris Nellåker, Christopher Wragg, Claire Kirk, Claire Turner, Daniel A. King, Daniel M. Barrett, Daniel Perrett, Daniela T. Pilz, Danielle Walker, David Baty, David Bohanna, David Bourn, David Goudie, David J. Bunyan, David Jones, David Moore, David Fitzpatrick, David Fitzpatrick, Debbie Rice, Debbie Shears, Deirdre Cilliers, Deirdre Donnelly, Denise Williams, Derek Lim
प्रकाशित 2017Artigo -
19
Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia द्वारा Kathleen M. Gorman, Esther Meyer, Detelina Grozeva, Egidio Spinelli, Amy McTague, Alba Sanchis‐Juan, Keren Carss, Emily Bryant, Adi Reich, Amy L. Schneider, Ronit Pressler, Michael A. Simpson, Geoff Debelle, Evangeline Wassmer, Jenny Morton, Diana Sieciechowicz, Eric Jan-Kamsteeg, Alex R. Paciorkowski, Mary D. King, J. Helen Cross, Annapurna Poduri, Heather C. Mefford, Ingrid E. Scheffer, Tobias B. Haack, Gary McCullagh, J Gordon Millichap, Gemma L. Carvill, Jill Clayton‐Smith, Eamonn R. Maher, F. Lucy Raymond, Manju A. Kurian, 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
प्रकाशित 2019Artigo
खोज साधन:
संबंधित विषय
Biology
Genetics
Gene
Medicine
Computational biology
Internal medicine
Mutation
Exome
Exome sequencing
Environmental health
Genotype
Pathology
Phenotype
Allele
Cancer research
Disease
Genome
Population
Antibody
Biochemistry
Cancer
Chemistry
Chemotherapy
Chromosome
Computer science
Copy-number variation
DNA sequencing
Epilepsy
Genome-wide association study
Genomics