Bibliography

PRICE, A.L, WEALE, M.E, PATTERSON, N, MYERS, S.R, NEED, A.C , SHIANNA, K.V, GE, D, ROTTER, J.I, TORRES, E, TAYLOR, K.D, GOLDSTEIN, D.B and REICH, D.  (2008)  Long-Range LD Can Confound Genome Scans in Admixed Populations.  American Journal of Human Genetics, 83(1),  132-135.

PRINGLE, M.  (1970)  The behaviour and adjustment of seven year-olds in England, Scotland and Wales: some comparative results from the National Child Development Study.  Scottish Educational Studies, 2, 45202.

PRINGLE, M.K.  (1965)  The National Child Development Study (1958 cohort).  Bulletin of the British Psychological Society, July, 45078.

PRINGLE, M.K.  (1969)  Policy implications of child development studies.  Concern, 3, 40-48.

PRINGLE, M.K.  (1972)  Born illegitimate (research feedback).  Concern, 8, 41456.

PRINGLE, M.K.  (1970)  Why are the most stable pupils found in Scotland?  Education, 136(14),  318 - 328.

PRINGLE, M.K.  (1969)  Regional differences in child behaviour.  Eugenic Society Bulletin, 1(4),  .

PRINGLE, M.K.  (1967)  Follow-up of adopted children.  Journal of the Medical Women's Federation, 43(3),  146-148.

PRINGLE, M.K.  (1968)  National Child Development Study (1958 cohort).  In unknown (ed), Research Relevant to the Education of Children with Learning Handicaps.

PRINGLE, M.K.  (1968)  Planning and programming for child care.  In unknown (ed), Selected Papers on Learning Difficulties. San Rafael California: Academic Therapy Publications.

PRINGLE, M.K, BUTLER, N.R and DAVIE, R.  (1966)  11,000 Seven-year-olds: First Report of the National Child Development Study (1958 Cohort).   London: Longman in association with the National Children's Bureau.

PRINS, B.P, KUCHENBAECKER, K.B, BAO, Y, SMART, M, ZABANEH, D, FATEMIFAR, G, LUAN, J’A, WAREHAM, N.J, SCOTT, R.A, PERRY, J.R.B, LANGENBERG, C, BENZEVAL, M, KUMARI, M and ZEGGINI, E.  (2017)  Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations.  Scientific Reports, 7, 11008.

PRIYA, S and MANAVALAN, R.  (2025)  Autoencoder with salp optimisation technique for exploring SNP-SNP interactions in Alzheimer's disease.  International Journal of Intelligent Engineering Informatics, 13(1),  55-77.

PROITSI, P, LUPTON, M.K, VELAYUDHAN, L, HUNTER, G, NEWHOUSE, S, LIN, K, FOGH, I, TSOLAKI, M, DANIILIDOU, M, PRITCHARD, M, CRAIG, D, TODD, S, JOHNSTON, J.A, McGUINNESS, B, KLOSZEWSKA, I, SOININEN, H, MECOCCI, P, VELLAS, B, PASSMORE, P.A, SIMS, R, WILLIAMS, J, BRAYNEL, C, the ALZHEIMER'S DISEASE NEUROIMAGING INITIATIVE and the GERAD1 CONSORTIUM.  (2014)  Alleles that increase risk for type 2 diabetes mellitus are not associated with increased risk for Alzheimer's disease.  Neurobiology of Aging, 35(12),  2883.e3–2883.e10.

PROITSI, P, LUPTON, M.K, VELAYUDHAN, L, NEWHOUSE, S, FOGH, I, TSOLAKI, M, DANIILIDOU, M, PRITCHARD, M, KLOSZEWSKA, I, SOININEN, H, MECOCCI, P, VELLAS, B, the ALZHEIMER'S DISEASE NEUROIMAGING INITIATIVE, WILLIAMS, J, the GERAD1 CONSORTIUM, STEWART, R, SHAM, P, LOVESTONE, S and POWELL, J.F.  (2014)  Genetic Predisposition to Increased Blood Cholesterol and Triglyceride Lipid Levels and Risk of Alzheimer Disease: A Mendelian Randomization Analysis.  PLoS Medicine, 11(9),  e1001713.

PROKOPENKO, I, ZEGGINI, E, HANSON, R.L, MITCHELL, B.D, RAYNER, N.W, AKAN, P, BAIER, L, DAS, S.K, ELLIOTT, K.S, FU, M, FRAYLING, T.M GROVES, C.J, GWILLIAM, R, SCOTT, L.J, VOIGHT, B.F, HATTERSLEY, A.T, HU, C, MORRIS, A.D, NG, M, PALMER, C.N, TELLO-RUIZ, M, VAXILLAIRE, M, WANG, C.R, STEIN, L, CHAN, J, JIA, W, FROGUEL, P, ELBEIN, S.C, DELOUKAS, P, BOGARDUS C, SHULDINER, A.R, McCARTHY, M.I and the INTERNATIONAL TYPE 2 DIABETES 1Q CONSORTIUM.  (2009)  Linkage disequilibrium mapping of the replicated type 2 diabetes linkage signal on chromosome 1q.  Diabetes, 58(7),  1704-1709.

PRONZATO, C. and AASSVE, A.  (2013)  Marital breakup and children's behavioural responses.  CHILD Working Papers Series 12_2013. Torino: Centre for Household, Income, Labour and Demographic Economics.

PROSSER,H.  (1973)  Family size and children's development.  Health and Social Service Journal, 432 (supplement), 45271.

PROUKAKIS, C, DUDZIK, C.G, BRIER, T, MACKAY, D.S, COOPER, J.M , MILLHAUSER, G.L, HOULDEN, H and SCHAPIRA, A.H.  (2013)  A novel a-synuclein missense mutation in Parkinson disease.  Neurology, 80(11),  1062-1064 .

PSYCHOSIS ENDOPHENOTYPES INTERNATIONAL CONSORTIUM and the WELLCOME TRUST CASE-CONTROL CONSORTIUM.  (2014)  A Genome-wide Association Analysis of a Broad Psychosis Phenotype Identifies Three Loci for Further Investigation.  Biological Psychiatry, 75(5),  386-397.