نتائج البحث - Ene‐Choo Tan
- يعرض 1 - 11 نتائج من 11
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Investigating analgesic and psychological factors associated with risk of postpartum depression development: a case–control study حسب Ban Leong Sng, Thangavelautham Suhitharan, Thi Phuong Tu Pham, Helen Chen, Pryseley Nkouibert Assam, Rehena Sultana, Ene‐Choo Tan, Nian-Lin Reena Han
منشور في 2016Artigo -
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A118G Single Nucleotide Polymorphism of Human μ-Opioid Receptor Gene Influences Pain Perception and Patient-controlled Intravenous Morphine Consumption after Intrathecal Morphine f... حسب Alex Tiong Heng Sia, Yvonne Lim, Eileen C.P. Lim, Rachelle W. C. Goh, Hai Yang Law, Ruth Landau, Yik-Ying Teo, Ene‐Choo Tan
منشور في 2008Artigo -
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Massively Parallel Sequencing of Patients with Intellectual Disability, Congenital Anomalies and/or Autism Spectrum Disorders with a Targeted Gene Panel حسب Maggie Brett, John R. McPherson, Zhi Jiang Zang, Angeline Lai, Ee-Shien Tan, Ivy Ng, Lai-choo Ong, Breana Cham, Patrick Tan, Steve Rozen, Ene‐Choo Tan
منشور في 2014Artigo -
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Combined analysis of 635 patients confirms an age-related association of the serotonin 2A receptor gene with tardive dyskinesia and specificity for the non-orofacial subtype حسب Bernard Lerer, Ronnen H. Segman, Ene‐Choo Tan, Vincenzo S. Basile, Roberto Cavallaro, H.N. Aschauer, Rael D. Strous, Siow-Ann Chong, Uriel Heresco‐Levy, M. Verga, Joachim Scharfetter, Herbert Y. Meltzer, James L. Kennedy, Fabìo Macciardi
منشور في 2005Revisão -
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ARCN1 Mutations Cause a Recognizable Craniofacial Syndrome Due to COPI-Mediated Transport Defects حسب Kosuke Izumi, Maggie Brett, Eriko Nishi, Séverine Drunat, Ee‐Shien Tan, Katsunori Fujiki, Sophie Lebon, Breana Cham, Koji Masuda, Michiko Arakawa, Adeline Jacquinet, Yusuke Yamazumi, Shu-Ting Chen, Alain Verloès, Yuki Okada, Yuki Katou, Tomohiko Nakamura, Tetsu Akiyama, Pierre Gressèns, Roger Foo, Sandrine Passemard, Ene‐Choo Tan, Vincent El Ghouzzi, Katsuhiko Shirahige
منشور في 2016Artigo -
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Review and Consensus on Pharmacogenomic Testing in Psychiatry حسب Chad A. Bousman, Susanne Bengesser, Katherine J. Aitchison, Azmeraw T. Amare, H.N. Aschauer, Bernhard T. Baune, Bahareh Behroozi Asl, Jeffrey R. Bishop, Margit Burmeister, Boris Chaumette, Li-Shiun Chen, Zachary A. Cordner, Jürgen Deckert, Franziska Degenhardt, Lynn E. DeLisi, Lasse Folkersen, James L. Kennedy, Teri E. Klein, Joseph L. McClay, Francis J. McMahon, Richard Musil, Nancy L. Saccone, Katrin Sangkuhl, Robert Stowe, Ene‐Choo Tan, Arun K. Tiwari, Clement C. Zai, Gwyneth Zai, Jianping Zhang, Andrea Gaedigk, Daniel J. Müller
منشور في 2020Revisão -
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PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature حسب Margot R.F. Reijnders, Robert Janowski, Mohsan Alvi, Jay Self, Ton J van Essen, Maaike Vreeburg, Rob P.W. Rouhl, Servi J.C. Stevens, Alexander P.A. Stegmann, Jolanda Schieving, Rolph Pfundt, Katinke van Dijk, Eric J. Smeets, Connie T. R. M. Stumpel, Levinus A. Bok, Jan Maarten Cobben, Marc Engelen, Sahar Mansour, Margo Whiteford, Kate Chandler, Sofia Douzgou, Nicola Cooper, Ene‐Choo Tan, Roger Foo, Angeline Lai, Julia Rankin, Andrew Green, Tuula Lönnqvist, Pirjo Isohanni, Shelley Williams, Ilene S. Ruhoy, Karen S. Carvalho, James J. Dowling, Dorit Lev, Katalin Štěrbová, Petra Laššuthová, Jana Neupauerová, Jeff L. Waugh, Sotirios Keros, Jill Clayton‐Smith, Sarah Smithson, Han G. Brunner, Ceciel van Hoeckel, Mel Anderson, Virginia E. Clowes, Victoria Mok Siu, the DDD study, Paulo Selber, Richard J. Leventer, Christoffer Nellåker, Dierk Niessing, David Hunt, Diana Baralle
منشور في 2017Revisão -
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Germline AGO2 mutations impair RNA interference and human neurological development حسب Davor Lessel, Daniela M. Zeitler, Margot R.F. Reijnders, Andriy Kazantsev, Fatemeh Hassani Nia, Alexander Bartholomäus, Victoria Martens, Astrid Bruckmann, Veronika Graus, Allyn McConkie‐Rosell, Marie McDonald, Bernarda Lozić, Ee‐Shien Tan, Erica H. Gerkes, Jessika Johannsen, Jonas Denecke, Aida Telegrafi, Evelien Zonneveld‐Huijssoon, Henny H. Lemmink, Breana Cham, Tanja Kovačević, Linda Ramsdell, Kimberly Foss, Diana Le Duc, Diana Mitter, Steffen Syrbe, Andreas Merkenschlager, Margje Sinnema, Bianca Panis, Joanna Lazier, Matthew Osmond, Taila Hartley, Jérémie Mortreux, Tiffany Busa, Chantal Missirian, Pankaj Prasun, Sabine Lüttgen, Ilaria Mannucci, Ivana Lessel, Claudia Schob, Stefan Kindler, John Pappas, Rachel Rabin, Marjolein H. Willemsen, Thatjana Gardeitchik, Katharina Löhner, Patrick Rump, Kerith‐Rae Dias, Carey‐Anne Evans, P. Ian Andrews, Tony Roscioli, Han G. Brunner, Chieko Chijiwa, M. E. Suzanne Lewis, Rami Abou Jamra, David A. Dyment, Kym M. Boycott, Alexander P.A. Stegmann, Christian Kubisch, Ene‐Choo Tan, Ghayda Mirzaa, Kirsty McWalter, Tjitske Kleefstra, Rolph Pfundt, Zoya Ignatova, Gunter Meister, Hans‐Jürgen Kreienkamp
منشور في 2020Artigo
أدوات البحث:
موضوعات ذات صلة
Medicine
Biology
Genetics
Internal medicine
Gene
Psychiatry
Anesthesia
Bioinformatics
Morphine
Opioid
Receptor
Analgesic
Cell biology
DNA sequencing
Genetic testing
Genotype
Mutation
Phenotype
Psychology
Anthropology
Argonaute
Autism
Autism spectrum disorder
Body mass index
COPI
COPII
Candidate gene
Carbamazepine
Compound heterozygosity
Computational biology