Getting ethics into practice: Clinicians need to be able to analyse and justify their day to day value judgments

od Parker, Michael J
Wydane 2004

Getting ethics into practice: Author's reply

od Parker, Michael J
Wydane 2004

Moral and scientific boundaries: research ethics on the Thai–Burma border

od Parker, Michael J
Wydane 2012

SARS-CoV-2 challenge studies: ethics and risk minimisation

od Bull, Susan, Jamrozik, Euzebiusz, Binik, Ariella, Parker, Michael J
Wydane w J Med Ethics (2021)

Ethics of instantaneous contact tracing using mobile phone apps in the control of the COVID-19 pandemic

od Parker, Michael J, Fraser, Christophe, Abeler-Dörner, Lucie, Bonsall, David
Wydane w J Med Ethics (2020)

PSD93 Regulates Synaptic Stability at Neuronal Cholinergic Synapses

od Parker, Michael J., Zhao, Shengli, Bredt, David S., Sanes, Joshua R., Feng, Guoping
Wydane w J Neurosci (2004)

Tigroid pattern of cerebral white matter involvement in chromosome 6p25 deletion syndrome with concomitant 5p15 duplication

od Balasubramanian, Meena, Smith, Kath, Williams, Steve, Griffiths, Paul D., Parker, Michael J., Mordekar, Santosh R.
Wydane w J Pediatr Genet (2012)

Heterogeneity of Nicotinic Receptor Class and Subunit mRNA Expression among Individual Parasympathetic Neurons from Rat Intracardiac Ganglia

od Poth, Kevin, Nutter, Thomas J., Cuevas, Javier, Parker, Michael J., Adams, David J., Luetje, Charles W.
Wydane w J Neurosci (1997)

Dominant Mutations in KAT6A Cause Intellectual Disability with Recognizable Syndromic Features

od Tham, Emma, Lindstrand, Anna, Santani, Avni, Malmgren, Helena, Nesbitt, Addie, Dubbs, Holly A., Zackai, Elaine H., Parker, Michael J., Millan, Francisca, Rosenbaum, Kenneth, Wilson, Golder N., Nordgren, Ann
Wydane w Am J Hum Genet (2015)

Mutations specific to the Rac-GEF domain of TRIO cause intellectual disability and microcephaly

od Pengelly, Reuben J, Greville-Heygate, Stephanie, Schmidt, Susanne, Seaby, Eleanor G, Jabalameli, M Reza, Mehta, Sarju G, Parker, Michael J, Goudie, David, Fagotto-Kaufmann, Christine, Mercer, Catherine, Debant, Anne, Ennis, Sarah, Baralle, Diana
Wydane w J Med Genet (2016)

Ethical Issues in Genetics and Infectious Diseases Research: An Interdisciplinary Expert Review

od Walker, Alexis, Bonham, Vence L., Boyce, Angie, Clayton, Ellen Wright, Garcia, Debra, Johnson, Stephanie, Laeyendecker, Oliver, Lewis, Michelle, Margolick, Joseph B., Mathews, Debra, Parker, Michael J., Spicer, Paul, Thio, Chloe L., Geller, Gail, Kahn, Jeffrey
Wydane w Ethics Med Public Health (2021)

Two families with sibling recurrence of the 17q21.31 microdeletion syndrome due to low-grade mosaicism

od Koolen, David A, Dupont, Juliette, de Leeuw, Nicole, Vissers, Lisenka ELM, van den Heuvel, Simone PA, Bradbury, Alyson, Steer, James, de Brouwer, Arjan PM, ten Kate, Leo P, Nillesen, Willy M, de Vries, Bert BA, Parker, Michael J
Wydane 2012

De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability

od Grozeva, Detelina, Carss, Keren, Spasic-Boskovic, Olivera, Parker, Michael J., Archer, Hayley, Firth, Helen V., Park, Soo-Mi, Canham, Natalie, Holder, Susan E., Wilson, Meredith, Hackett, Anna, Field, Michael, Floyd, James A.B., Hurles, Matthew, Raymond, F. Lucy
Wydane 2014

De novo, heterozygous, loss‐of‐function mutations in SYNGAP1 cause a syndromic form of intellectual disability

od Parker, Michael J., Fryer, Alan E., Shears, Deborah J., Lachlan, Katherine L., McKee, Shane A., Magee, Alex C., Mohammed, Shehla, Vasudevan, Pradeep C., Park, Soo‐Mi, Benoit, Valérie, Lederer, Damien, Maystadt, Isabelle, study, DDD, FitzPatrick, David R.
Wydane w Am J Med Genet A (2015)

PROCalcitonin-based algorithm for antibiotic use in Acute Pancreatitis (PROCAP): study protocol for a randomised controlled trial

od Siriwardena, Ajith K., Jegatheeswaran, Santhalingam, Mason, James M., Baltatzis, Minas, Chan, Anthony, Sheen, Aali J., O’Reilly, Derek, Jamdar, Saurabh, Deshpande, Rahul, de Liguori Carino, Nicola, Satyadas, Thomas, Qamruddin, Ahmed, Hayden, Katharine, Parker, Michael J., Butler, John, Rajai, Azita, McIntyre, Ben
Wydane w Trials (2019)

Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1133 families with developmental disorders

od Wright, Caroline F., McRae, Jeremy F., Clayton, Stephen, Gallone, Giuseppe, Aitken, Stuart, FitzGerald, Tomas W., Jones, Philip, Prigmore, Elena, Rajan, Diana, Lord, Jenny, Sifrim, Alejandro, Kelsell, Rosemary, Parker, Michael J., Barrett, Jeffrey C., Hurles, Matthew E., FitzPatrick, David R., Firth, Helen V.
Wydane w Genet Med (2018)

Mutations in LRP5 or FZD4 Underlie the Common Familial Exudative Vitreoretinopathy Locus on Chromosome 11q

od Toomes, Carmel, Bottomley, Helen M., Jackson, Richard M., Towns, Katherine V., Scott, Sheila, Mackey, David A., Craig, Jamie E., Jiang, Li, Yang, Zhenglin, Trembath, Richard, Woodruff, Geoffrey, Gregory-Evans, Cheryl Y., Gregory-Evans, Kevin, Parker, Michael J., Black, Graeme C. M., Downey, Louise M., Zhang, Kang, Inglehearn, Chris F.
Wydane 2004

Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders

od Faundes, Víctor, Newman, William G., Bernardini, Laura, Canham, Natalie, Clayton-Smith, Jill, Dallapiccola, Bruno, Davies, Sally J., Demos, Michelle K., Goldman, Amy, Gill, Harinder, Horton, Rachel, Kerr, Bronwyn, Kumar, Dhavendra, Lehman, Anna, McKee, Shane, Morton, Jenny, Parker, Michael J., Rankin, Julia, Robertson, Lisa, Temple, I. Karen, Banka, Siddharth
Wydane w Am J Hum Genet (2018)

Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data

od Aitken, Stuart, Firth, Helen V., McRae, Jeremy, Halachev, Mihail, Kini, Usha, Parker, Michael J., Lees, Melissa M., Lachlan, Katherine, Sarkar, Ajoy, Joss, Shelagh, Splitt, Miranda, McKee, Shane, Németh, Andrea H., Scott, Richard H., Wright, Caroline F., Marsh, Joseph A., Hurles, Matthew E., FitzPatrick, David R.
Wydane w Am J Hum Genet (2019)

Structural analysis of pathogenic mutations in the DYRK1A gene in patients with developmental disorders

od Evers, Jochem M.G., Laskowski, Roman A., Bertolli, Marta, Clayton-Smith, Jill, Deshpande, Charu, Eason, Jacqueline, Elmslie, Frances, Flinter, Frances, Gardiner, Carol, Hurst, Jane A., Kingston, Helen, Kini, Usha, Lampe, Anne K., Lim, Derek, Male, Alison, Naik, Swati, Parker, Michael J., Price, Sue, Robert, Leema, Sarkar, Ajoy, Straub, Volker, Woods, Geoff, Thornton, Janet M., Wright, Caroline F.
Wydane w Hum Mol Genet (2017)