Resultados da pesquisa - Rachel Horton
- A mostrar 1 - 18 resultados de 18
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Recent developments in genetic/genomic medicine Por Rachel Horton, Anneke Lucassen
Publicado em 2019Revisão -
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Consent and Autonomy in the Genomics Era Por Rachel Horton, Anneke Lucassen
Publicado em 2019Revisão -
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Gender Identity 5 Years After Social Transition Por Kristina R. Olson, Lily Durwood, Rachel Horton, Natalie M. Gallagher, Aaron Devor
Publicado em 2022Artigo -
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Direct-to-consumer genetic testing Por Rachel Horton, Gillian Crawford, Lindsey Freeman, Angela Fenwick, Caroline F. Wright, Anneke Lucassen
Publicado em 2019Editorial -
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Nonpharmacological Management of Procedural Pain in Infants and Young Children: An Abridged Cochrane Review Por Rebecca Pillai Riddell, Nicole Racine, Kara Turcotte, Lindsay S Uman, Rachel Horton, Laila Din Osmun, Sara Ahola Kohut, Jessica Hillgrove Stuart, Bonnie Stevens, Diana Lisi
Publicado em 2011Revisão -
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Burkholderia pseudomallei Penetrates the Brain via Destruction of the Olfactory and Trigeminal Nerves: Implications for the Pathogenesis of Neurological Melioidosis Por James A. St John, Jenny Ekberg, Samantha J. Dando, Adrian Cuda Banda Meedeniya, Rachel Horton, Michael R. Batzloff, Suzzanne Owen, Stephanie Holt, Ian R. Peak, Glen C. Ulett, Alan Mackay‐Sim, Ifor R. Beacham
Publicado em 2014Artigo -
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The ethical challenges of diversifying genomic data: A qualitative evidence synthesis Por Faranak Hardcastle, Kate Lyle, Rachel Horton, Gabrielle Samuel, Susie Weller, Lisa Ballard, Rachel Thompson, Luiz Valério de Paula Trindade, José David Gómez Urrego, Daniel Kochin, Tess Johnson, Nechama Tatz-Wieder, Elizabeth Redrup Hill, Florence Robinson Adams, Yoseph Eskandar, Eli Harriss, Krystal S. Tsosie, Padraig Dixon, Maxine Mackintosh, Lyra Nightingale, Anneke Lucassen
Publicado em 2023Artigo -
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Maternal variants in <i>NLRP</i> and other maternal effect proteins are associated with multilocus imprinting disturbance in offspring Por Matthias Begemann, Faisal I. Rezwan, Jasmin Beygo, Louise E Docherty, Julia Kolarova, Christopher Schroeder, Karin Buiting, Kamal Chokkalingam, Franziska Degenhardt, Emma Wakeling, Stephanie Kleinle, Daniela González Fassrainer, Barbara Oehl‐Jaschkowitz, Claire Turner, Michał Patalan, Maria Giżewska, Gerhard Binder, Cấn Thị Bích Ngọc, Vũ Chí Dũng, Sarju Mehta, Gareth Baynam, Julian Hamilton‐Shield, Sara Aljareh, Oluwakemi Lokulo‐Sodipe, Rachel Horton, Reiner Siebert, Miriam Elbracht, I. Karen Temple, Thomas Eggermann, Deborah Mackay
Publicado em 2018Artigo -
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Quantifying the contribution of recessive coding variation to developmental disorders Por Hilary C. Martin, Wendy D. Jones, Rebecca E. McIntyre, Gabriela Sánchez-Andrade, Mark Sanderson, James Stephenson, Carla P. Jones, Juliet Handsaker, Giuseppe Gallone, Michaela Bruntraeger, Jeremy F. McRae, Elena Prigmore, Patrick Short, Mari Niemi, Joanna Kaplanis, Elizabeth J. Radford, Nadia Akawi, Meena Balasubramanian, John Dean, Rachel Horton, Alice Hulbert, Diana Johnson, Katie Johnson, Dhavendra Kumar, Sally Ann Lynch, Sarju Mehta, Jenny Morton, Michael Parker, Miranda Splitt, Peter D. Turnpenny, Pradeep Vasudevan, Michael Wright, Andrew Bassett, Sebastian S. Gerety, Caroline F. Wright, David Fitzpatrick, Helen V. Firth, Matthew E. Hurles, Jeffrey C. Barrett
Publicado em 2018Artigo -
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Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders Por 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
Publicado em 2017Artigo
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Assuntos relacionados
Biology
Genetics
Medicine
Psychology
Gene
Computer science
Developmental psychology
Genome
Law
Paleontology
Pathology
Political science
Social psychology
Data science
Engineering
Engineering ethics
Gene expression
Phenotype
Computational biology
Context (archaeology)
DNA methylation
Epigenetics
Genetic testing
Genomics
Immunology
Internal medicine
Internet privacy
Pain management
Programming language
Sociology