People

Dr John Dean

Dr John Dean
Dr John Dean
Dr John Dean

MA, MBChB, FRCP, FRCPE

Emeritus Reader

About
Email Address
j.dean@abdn.ac.uk
Telephone Number
+44 (0)1224 552501
Office Address

Clinical Genetics,

Ashgrove House,

Forestehill,

Aberdeen

School/Department
School of Medicine, Medical Sciences and Nutrition

British Society for Genetic Medicine

The BSGM has recently published a report on the Retention of Genetic Family Records, accessible below:

BSGM Report on the Retention of Genetic Family Records

External Memberships

Secretary of the British Society for Genetic Medicine

Latest Publications

  • Renin-Angiotensin System inhibitors (RASi) are not nephrotoxic - they protect the kidneys and the heart

    Murray, J. S., Kalra, P. R., Anderson, L. J., Selby, N. M., Sawhney, S., McKane, W. S., Ostermann, M., Kohle, N. V., McWilliam, S. J., Nagalingam, K., Bickerton, S., Lewington, A. J., Hinchliffe, W. T., Smith, S. J., Wise, M., Hancock, A., Kingdon, E., Cockwell, P., James, M. T., Blakeman, T., Dean, J. D., Morlidge, C., Tomlinson, L. A., Green, D.
    Clinical Medicine, vol. 26, no. 3, 100577
    Contributions to Journals: Articles

  • Actionable genetic variants in 4,198 Scottish participants from the Orkney and Shetland founder populations and implementation of return of results

    Kerr, S. M., Klaric, L., Muckian, M. D., Johnston, K., Drake, C., Halachev, M., Cowan, E., Snadden, L., Dean, J., Zheng, S. L., Thami, P. K., Ware, J. S., Tzoneva, G., Shuldiner, A. R., Miedzybrodzka, Z., Wilson, J. F.
    American Journal of Human Genetics, vol. 112, no. 4, pp. 793-807
    Contributions to Journals: Articles

  • An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort

    Kerr, S. M., Klaric, L., Halachev, M., Hayward, C., Boutin, T. S., Meynert, A. M., Semple, C. A., Tuiskula, A. M., Swan, H., Santoyo-Lopez, J., Vitart, V., Haley, C., Dean, J., Miedzybrodzka, Z., Aitman, T. J., Wilson, J. F.
    Scientific Reports, vol. 9, 10964
    Contributions to Journals: Articles

  • Parents’ views of genetic testing and treatment of familial hypercholesterolemia in children: a qualitative study

    Keenan, K. F., Finnie, R. M., Simpson, W. G., McKee, L., Dean, J., Miedzybrodzka, Z.
    Journal of Community Genetics, vol. 10, no. 1, pp. 129-141
    Contributions to Journals: Articles

  • CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018)

    Blok, L. S., Rousseau, J., Twist, J., Ehresmann, S., Takaku, M., Venselaar, H., Rodan, L. H., Nowak, C. B., Douglas, J., Swoboda, K. J., Steeves, M. A., Sahai, I., Stumpel, C. T. R. M., Stegmann, A. P. A., Wheeler, P., Willing, M., Fiala, E., Kochhar, A., Gibson, W. T., Cohen, A. S. A., Agbahovbe, R., Innes, A. M., Au, P. Y. B., Rankin, J., Anderson, I. J., Skinner, S. A., Louie, R. J., Warren, H. E., Afenjar, A., Keren, B., Nava, C., Buratti, J., Isapof, A., Rodriguez, D., Lewandowski, R., Propst, J., van Essen, T., Choi, M., Lee, S., Chae, J. H., Price, S., Schnur, R. E., Douglas, G., Wentzensen, I. M., Zweier, C., Reis, A., D'Alessandro, M., Dean, J., Miedzybrodzka, Z., Ross, A., DDD Study
    Nature Communications, vol. 9, 4619
    Contributions to Journals: Articles

View My Publications

Research

Research Overview

Inherited cardiac conditions, epilepsy and learning disability, genomic medicine

Publications

Page 1 of 2 Results 1 to 10 of 15

  • Renin-Angiotensin System inhibitors (RASi) are not nephrotoxic - they protect the kidneys and the heart

    Murray, J. S., Kalra, P. R., Anderson, L. J., Selby, N. M., Sawhney, S., McKane, W. S., Ostermann, M., Kohle, N. V., McWilliam, S. J., Nagalingam, K., Bickerton, S., Lewington, A. J., Hinchliffe, W. T., Smith, S. J., Wise, M., Hancock, A., Kingdon, E., Cockwell, P., James, M. T., Blakeman, T., Dean, J. D., Morlidge, C., Tomlinson, L. A., Green, D.
    Clinical Medicine, vol. 26, no. 3, 100577
    Contributions to Journals: Articles

  • Actionable genetic variants in 4,198 Scottish participants from the Orkney and Shetland founder populations and implementation of return of results

    Kerr, S. M., Klaric, L., Muckian, M. D., Johnston, K., Drake, C., Halachev, M., Cowan, E., Snadden, L., Dean, J., Zheng, S. L., Thami, P. K., Ware, J. S., Tzoneva, G., Shuldiner, A. R., Miedzybrodzka, Z., Wilson, J. F.
    American Journal of Human Genetics, vol. 112, no. 4, pp. 793-807
    Contributions to Journals: Articles

  • An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort

    Kerr, S. M., Klaric, L., Halachev, M., Hayward, C., Boutin, T. S., Meynert, A. M., Semple, C. A., Tuiskula, A. M., Swan, H., Santoyo-Lopez, J., Vitart, V., Haley, C., Dean, J., Miedzybrodzka, Z., Aitman, T. J., Wilson, J. F.
    Scientific Reports, vol. 9, 10964
    Contributions to Journals: Articles

  • Parents’ views of genetic testing and treatment of familial hypercholesterolemia in children: a qualitative study

    Keenan, K. F., Finnie, R. M., Simpson, W. G., McKee, L., Dean, J., Miedzybrodzka, Z.
    Journal of Community Genetics, vol. 10, no. 1, pp. 129-141
    Contributions to Journals: Articles

  • CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018)

    Blok, L. S., Rousseau, J., Twist, J., Ehresmann, S., Takaku, M., Venselaar, H., Rodan, L. H., Nowak, C. B., Douglas, J., Swoboda, K. J., Steeves, M. A., Sahai, I., Stumpel, C. T. R. M., Stegmann, A. P. A., Wheeler, P., Willing, M., Fiala, E., Kochhar, A., Gibson, W. T., Cohen, A. S. A., Agbahovbe, R., Innes, A. M., Au, P. Y. B., Rankin, J., Anderson, I. J., Skinner, S. A., Louie, R. J., Warren, H. E., Afenjar, A., Keren, B., Nava, C., Buratti, J., Isapof, A., Rodriguez, D., Lewandowski, R., Propst, J., van Essen, T., Choi, M., Lee, S., Chae, J. H., Price, S., Schnur, R. E., Douglas, G., Wentzensen, I. M., Zweier, C., Reis, A., D'Alessandro, M., Dean, J., Miedzybrodzka, Z., Ross, A., DDD Study
    Nature Communications, vol. 9, 4619
    Contributions to Journals: Articles

  • Phenotype-driven molecular autopsy for sudden cardiac death

    Cann, F., Corbett, M., O'Sullivan, D., Tennant, S., Hailey, H., Grieve, J. H. K., Broadhurst, P., Rankin, R., Dean, J. C. S.
    Clinical Genetics, vol. 91, no. 1, pp. 22-29
    Contributions to Journals: Articles

  • Structural and electrical cardiac abnormalities are prevalent in asymptomatic adults with myotonic dystrophy

    Choudhary, P., Nandakumar, R., Greig, H., Broadhurst, P., Dean, J., Puranik, R., Celermajer, D. S., Hillis, G. S.
    Heart, vol. 102, no. 18, pp. 1472-1478
    Contributions to Journals: Articles

  • A New, Atypical Case of Cobalamin F Disorder Diagnosed by Whole Exome Sequencing

    Constantinou, P., Lochhead, P., D'Allesandro, M., Samant, S., Deciphering Developmental Disorders Study, Dean, J., Hauptfleisch, C.
    Molecular Syndromology, vol. 6, pp. 254-258
    Contributions to Journals: Articles

  • A high frequency of the MTHFR 677C > T polymorphism in Scottish women with epilepsy: Possible role in pathogenesis

    Dean, J., Robertson, Z., Reid, V., Wang, Q., Hailey, H., Moore, S., Rasalam, A. D., Turnpenny, P., Lloyd, D., Shaw, D., Little, J.
    Seizure, vol. 17, no. 3, pp. 269-275
    Contributions to Journals: Articles

  • Marfan syndrome: clinical diagnosis and management

    Dean, J. C.
    EJHG : European journal of human genetics : the official journal of the European Society of Human Genetics. , vol. 15, no. 7, pp. 724-733
    Contributions to Journals: Articles
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