Canlyniadau Chwilio - Robyn V. Jamieson

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  1. 1
    Domain disruption and mutation of the bZIP transcription factor, MAF,associated with cataract, ocular anterior segment dysgenesis and coloboma

    Domain disruption and mutation of the bZIP transcription factor, MAF,associated with cataract, ocular anterior segment dysgenesis and coloboma gan Robyn V. Jamieson

    Cyhoeddwyd 2002
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  2. 2
    Masquerade macular exudation in Mallatia Leventinese

    Masquerade macular exudation in Mallatia Leventinese gan Shaun Y.P. Ewe, Robyn V. Jamieson, Andrew Chang

    Cyhoeddwyd 2016
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    Carta
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  3. 3
    Neurofibromatosis Type 1: Review and Update on Emerging Therapies

    Neurofibromatosis Type 1: Review and Update on Emerging Therapies gan Tanya Karaconji, Eline Whist, Robyn V. Jamieson, Maree Flaherty, John Grigg

    Cyhoeddwyd 2018
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    Revisão
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  4. 4
    What is the power of a genomic multidisciplinary team approach? A systematic review of implementation and sustainability

    What is the power of a genomic multidisciplinary team approach? A systematic review of implementation and sustainability gan Alan Ma, Rosie O’Shea, Laura Wedd, Claire Wong, Robyn V. Jamieson, Nicole Rankin

    Cyhoeddwyd 2024
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    Revisão
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  5. 5
    Secondary glaucoma after paediatric cataract surgery

    Secondary glaucoma after paediatric cataract surgery gan Brighu Swamy, F. A. Billson, Francisco J. Plaza Martín, Craig Donaldson, Stephen Hing, Robyn V. Jamieson, John Grigg, James E. Smith

    Cyhoeddwyd 2007
    Cael y testun llawn
    Artigo
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  6. 6
    Hardy-Rand-Rittler colour vision testing in cone and cone-rod dystrophies: correlation with structural and functional outcome measures

    Hardy-Rand-Rittler colour vision testing in cone and cone-rod dystrophies: correlation with structural and functional outcome measures gan B. Tharmarajah, Elisa E. Cornish, Jonathan V. Nguyen, Elizabeth H Barnes, Kate E. Leahy, Anagha Vaze, Robyn V. Jamieson, John Grigg

    Cyhoeddwyd 2025
    Cael y testun llawn
    Artigo
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  7. 7
    Comprehensive characterization of fetal and mature retinal cell identity to assess the fidelity of retinal organoids

    Comprehensive characterization of fetal and mature retinal cell identity to assess the fidelity of retinal organoids gan Hani Jieun Kim, Michelle O’Hara-Wright, Daniel Kim, To Ha Loi, Benjamin Y. Lim, Robyn V. Jamieson, Anai Gonzalez-Cordero, Pengyi Yang

    Cyhoeddwyd 2023
    Cael y testun llawn Cael y testun llawn
    Artigo
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  8. 8
    Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1

    Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1 gan Ivan Prokudin, Cas Simons, John Grigg, Rebecca Storen, Vikrant Kumar, Zai Yang Phua, James E. Smith, Maree Flaherty, Sonia Dávila, Robyn V. Jamieson

    Cyhoeddwyd 2013
    Cael y testun llawn
    Artigo
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  9. 9
    <i>Dkk1</i>and<i>Wnt3</i>interact to control head morphogenesis in the mouse

    <i>Dkk1</i>and<i>Wnt3</i>interact to control head morphogenesis in the mouse gan Samara E. Lewis, Poh‐Lynn Khoo, Reginald Young, Kirsten A. Steiner, Chris Wilcock, Mahua Mukhopadhyay, Heiner Westphal, Robyn V. Jamieson, Lorraine Robb, Patrick Tam

    Cyhoeddwyd 2008
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    Artigo
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  10. 10
    Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next‐Generation Sequencing

    Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next‐Generation Sequencing gan Alan Ma, John Grigg, Gladys Ho, Ivan Prokudin, Elizabeth Farnsworth, Katherine Holman, Anson Cheng, Frank A. Billson, Frank Martin, Clare L. Fraser, David Mowat, James E. Smith, John Christodoulou, Maree Flaherty, Bruce Bennetts, Robyn V. Jamieson

    Cyhoeddwyd 2015
    Cael y testun llawn Cael y testun llawn
    Artigo
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  11. 11
    An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation

    An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation gan G. Cederquist, Anna Łuchniak, Max A. Tischfield, Maya Peeva, Yuyu Song, Manoj P. Menezes, Wai‐Man Chan, Caroline Andrews, Sheena Chew, Robyn V. Jamieson, Lavier Gomes, Maree Flaherty, P. Ellen Grant, Mohan L. Gupta, Elizabeth C. Engle

    Cyhoeddwyd 2012
    Cael y testun llawn
    Artigo
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  12. 12
    Dismantling barriers to research and clinical care for individuals with a vision impairment

    Dismantling barriers to research and clinical care for individuals with a vision impairment gan Eden G. Robertson, Kate Hetherington, Meredith Prain, James Hall, Lydia Boyd, Rosemary Boyd OAM, Emily L. C. Shepard, Hollie Feller, Sally Karandrews, Fleur O’Hare, Kohji Yamamoto, Matthew P. Simunovic, Robyn V. Jamieson, Alan Ma, Lauren N. Ayton, Anai Gonzalez‐Cordero

    Cyhoeddwyd 2025
    Cael y testun llawn Cael y testun llawn
    Artigo
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  13. 13
    Mutations in<i>SIPA1L3</i>cause eye defects through disruption of cell polarity and cytoskeleton organization

    Mutations in<i>SIPA1L3</i>cause eye defects through disruption of cell polarity and cytoskeleton organization gan Rebecca Greenlees, Marija Mihelec, Saira Yousoof, Daniel Speidel, Selwin K. Wu, Silke Rinkwitz, Ivan Prokudin, Rahat Perveen, Anson Cheng, Alan Ma, Benjamin M. Nash, Rachel Gillespie, David A.F. Loebel, Jill Clayton‐Smith, I. Christopher Lloyd, John Grigg, Patrick Tam, Alpha S. Yap, Thomas Becker, Graeme Black, Elena V. Semina, Robyn V. Jamieson

    Cyhoeddwyd 2015
    Cael y testun llawn Cael y testun llawn
    Artigo
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  14. 14
    Revealing hidden genetic diagnoses in the ocular anterior segment disorders

    Revealing hidden genetic diagnoses in the ocular anterior segment disorders gan Alan Ma, Saira Yousoof, John Grigg, Maree Flaherty, André E. Minoche, Mark J. Cowley, Benjamin M. Nash, Gladys Ho, Thet Gayagay, Tiffany Lai, Elizabeth Farnsworth, Emma L. Hackett, Katrina Fisk, Karen Wong, Katherine Holman, Gemma Jenkins, Anson Cheng, Frank Martin, Tanya Karaconji, James E. Elder, Annabelle Enriquez, Meredith Wilson, David J. Amor, Chloe Stutterd, Benjamin Kamien, John W. Nelson, Marcel E. Dinger, Bruce Bennetts, Robyn V. Jamieson

    Cyhoeddwyd 2020
    Cael y testun llawn Cael y testun llawn
    Artigo
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  15. 15
    Gene selection for the Australian Reproductive Genetic Carrier Screening Project (“Mackenzie’s Mission”)

    Gene selection for the Australian Reproductive Genetic Carrier Screening Project (“Mackenzie’s Mission”) gan Edwin P. Kirk, Royston Ong, Kirsten Boggs, Tristan Hardy, Sarah Righetti, Ben Kamien, Tony Roscioli, David J. Amor, Madhura Bakshi, Clara W. T. Chung, Alison Colley, Robyn V. Jamieson, Jan Liebelt, Alan Ma, Nicholas Pachter, Sulekha Rajagopalan, Anja Ravine, Meredith Wilson, Jade Caruana, Rachael Casella, Mark R. Davis, Samantha Edwards, Alison D. Archibald, Julie McGaughran, Ainsley J. Newson, Nigel G. Laing, Martin B. Delatycki

    Cyhoeddwyd 2020
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    Artigo
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  16. 16
    Detection of Chromosomal Breakpoints in Patients with Developmental Delay and Speech Disorders

    Detection of Chromosomal Breakpoints in Patients with Developmental Delay and Speech Disorders gan Kagistia Hana Utami, Axel M. Hillmer, Irène Aksoy, Elaine Guo Yan Chew, Audrey S.M. Teo, Zhenshui Zhang, Charlie W. H. Lee, Pauline J. Chen, Chan Chee Seng, Pramila Ariyaratne, Sigrid Rouam, Lim Seong Soo, Saira Yousoof, Ivan Prokudin, Gregory B. Peters, Felicity Collins, Meredith Wilson, Alyson Kakakios, Georges Haddad, Arnaud Menuet, Olivier Perche, S K Tay, Wing‐Kin Sung, Xiaoan Ruan, Yijun Ruan, Edison T. Liu, Sylvain Briault, Robyn V. Jamieson, Sonia Dávila, Valère Cacheux

    Cyhoeddwyd 2014
    Cael y testun llawn Cael y testun llawn
    Artigo
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  17. 17
    ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder

    ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder gan Lewis Williams, Asif Javed, Amin Sabri, Denise J. Morgan, Chad Huff, John Grigg, Xiu Ting Heng, Alexis Jiaying Khng, Iris H.I.M. Hollink, Margaux A. Morrison, Leah A. Owen, Katherine Anderson, Krista Kinard, Rebecca Greenlees, Danica Novacic, Sen Hou, Wadih M. Zein, George M. Rodgers, Albert T. Vitale, Neena B. Haider, Axel M. Hillmer, Pauline C. Ng, Shankaracharya, Anson Cheng, Linda Zheng, Mark C. Gillies, Marjon van Slegtenhorst, P. Martin van Hagen, Tom Missotten, Gary L. Farley, Michael Polo, J. Jeffrey Malatack, Julie Curtin, Frank Martin, Susan Arbuckle, Stephen I. Alexander, Megan Chircop, Sonia Dávila, Kathleen B. Digre, Robyn V. Jamieson, Margaret M. DeAngelis

    Cyhoeddwyd 2019
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    Artigo
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  18. 18
    Retinal Dystrophies Associated With Peripherin-2: Genetic Spectrum and Novel Clinical Observations in 241 Patients

    Retinal Dystrophies Associated With Peripherin-2: Genetic Spectrum and Novel Clinical Observations in 241 Patients gan Rachael C. Heath Jeffery, Jennifer A Thompson, Johnny Lo, Enid S. Chelva, Sean Armstrong, Jose S. Pulido, Rebecca Procopio, Andrea L. Vincent, Lorenzo Bianco, Maurízio Battaglia Parodi, Lucia Ziccardi, Giulio Antonelli, Lucilla Barbano, João P. Marques, Sara Geada, Ana L. Carvalho, Wei C. Tang, Choi M. Chan, Camiel J.F. Boon, Jonathan Hensman, Ta‐Ching Chen, Chien-Yu Lin, Pei-Lung Chen, Ajoy Vincent, Anupreet Tumber, Elise Heon, John Grigg, Robyn V. Jamieson, Elisa E. Cornish, Benjamin M. Nash, Shyamanga Borooah, Lauren N. Ayton, Alexis Ceecee Britten-Jones, Thomas L. Edwards, Jonathan B. Ruddle, Abhishek Sharma, Rowan GB Porter, Tina M. Lamey, Terri L. McLaren, Samuel McLenachan, Danial Roshandel, Fred K. Chen

    Cyhoeddwyd 2024
    Cael y testun llawn Cael y testun llawn
    Artigo
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  19. 19
    Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance

    Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance gan Max A. Tischfield, Hagit Baris, Chen Wu, Guenther Rudolph, Lionel Van Maldergem, Wei He, Wai‐Man Chan, Caroline Andrews, Joseph L. Demer, Richard L. Robertson, David A. Mackey, Jonathan B. Ruddle, Thomas D. Bird, Irène Gottlob, Christina Pieh, Elias I. Traboulsi, Scott L. Pomeroy, David G. Hunter, Janet S. Soul, Anna Newlin, Louise J. Sabol, Edward J. Doherty, Clara E. de Uzcátegui, Nicolas Uzcategui, Mary Louise Z. Collins, Emin Cumhur Şener, Bettina Wabbels, Heide Hellebrand, Thomas Meitinger, Teresa de Berardinis, Adriano Magli, Costantino Schiavi, Marco Pastore-Trossello, Feray Koc, Agnes Wong, Alex V. Levin, Michael T. Geraghty, Maria Descartes, Maree Flaherty, Robyn V. Jamieson, Hans Ulrik Møller, I. Meuthen, David F. Callen, Janet Kerwin, Susan Lindsay, Alfons Meindl, Mohan L. Gupta, David Pellman, Elizabeth C. Engle

    Cyhoeddwyd 2010
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    Artigo
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