Bibliography

ROSS, E, PECKHAM, C, WEST, P and BUTLER, N.R.  (1980)  Epilepsy in childhood: findings from the National Child Development Study.  British Medical Journal, 280(6209),  207-210.

ROSS, E.M, KURTZ, Z and PECKHAM, C.  (1983)  Children with Epilepsy: Implications for the School Health Service.  Public Health, 97, 75-81.

ROSS, E.M and PECKHAM, C.S.  (1983)  Seizure disorders in the National Child Development Study.  In ROSE, F.C (ed), Advances in Epilepsy. London: Pitman Medical.

ROSS, E.M and TOOKEY, P.  (1988)  Educational needs and epilepsy in childhood.  In TRIMBLE, M.R and REYNOLDS, E.H (ed), Epilepsy, behaviour and cognitive function. Chichester: John Wiley.

ROSS, E.M and WEST, P.B.  (1978)  Achievement and problems of British eleven year olds with epilepsy.  In MEINARDI, H and ROWAN, A.J (ed), Advances in Epileptology. New York: Swets & Zeitlinger.

ROSS,E M.  (1973)  Convulsive disorders in British children.  Proceedings of the Royal Society of Medicine, 66(7),  703-704.

ROSS,E M.  (1973)  Some nutritional aspects of large scale prospective studies in child development.  In HOLLINGSWORTH,D and RUSSELL,M (ed), Nutritional Problems in a Changing World. London: Applied Science Publications.

ROTHSCHILD, D, WEISSBROD, O, BARKAN, E, KURILSHIKOV, A, KOREM, T, ZEEVI, D, COSTEA, P.I, GODNEVA, A, KALKA, I.N, BAR, N, SHILO, S, LADOR, D, VICH VILA, A, ZMORA, N, PEVSNER-FISCHER, M, ISRAELI, D, KOSOWER, N, MALKA, G, CHEN WOLF, B, AVNIT-SAGI, T, LOTAN-POMPAN, M, WEINBERGER, A, HALPERN, Z, CARMI, S, FU, J, WIJMENGA, C, ZHERNAKOVA, A, ELINAV, E and SEGAL, E.  (2018)  Environment dominates over host genetics in shaping human gut microbiota.  Nature, 555, 210-215.

ROUGEAUX, E, PEARCE, A and LAW, C.  (2014)  Inequality in early adolescent health in the UK Millennium Cohort Study (2011/12): Emeline Rougeaux.  European Journal of Public Health, 24(Suppl.2),  41913.

ROUGEAUX, E., HOPE, S., LAW, C. and PEARCE, A..  (2017)  Have health inequalities changed during childhood in the New Labour generation? Findings from the UK Millennium Cohort Study.  BMJ Open, 7(1),  42746.

ROUGEAUX, E., HOPE, S., VINER, R.M., DEIGHTON, J., LAW, C. and PEARCE, A.  (2020)  Is Mental Health Competence in Childhood Associated With Health Risk Behaviors in Adolescence? Findings From the UK Millennium Cohort Study.  Journal of Adolescent Health, 67(5),  677-684.

ROUXEL, P and CHANDOLA, T.  (2024)  No Substitute for In-Person Interaction: Changing Modes of Social Contact during the Coronavirus Pandemic and Effects on the Mental Health of Adults in the UK.  Sociology, 58(2),  330-350.

ROWLANDS, T.  (2024)  Text mining and integration of genetic association information.  Doctoral thesis.University of Leicester.

ROWLINGSON, K and McKAY, S.  (2005)  Lone motherhood and socio-economic disadvantage: Insights from quantitative and qualitative evidence.  The Sociological Review, 53(1),  30-49.

ROYA, P, ALIA, A.J, KOBIYAMA, K, GHOSHEH, Y and LEY, K.  (2020)  Opportunities for an atherosclerosis vaccine: From mice to humans.  Vaccine, 38(28),  4495-4506.

ROZANSKI, S., SCHMIDT, A., JOHN, A. and GAYSINA, D.  (2021)  Childhood neglect and trajectories of affective symptoms throughout adulthood: a British birth cohort study.  Journal of Affective Disorders, 295, 416-421.

RUARK, E, MÜNZ, M, CLARKE, M, RENWICK, A, RAMSAY, E, ELLIOTT, A, SEAL, S, LUNTER, G and RAHMAN, N.  (2016)  OpEx - a validated, automated pipeline optimised for clinical exome sequence analysis.  Scientific Reports, 6, 31029.

RUARK, E, MÜNZ, M, RENWICK, A, CLARKE, M, RAMSAY, E, HANKS, S, MAHAMDALLIE, S ELLIOTT, A, SEAL, S, STRYDOM, A, GERTON, L and RAHMAN, N.  (2015)  The ICR1000 UK exome series: a resource of gene variation in an outbred population.  F1000 Research, 4, 883.

RUARK, E, SNAPE, K, HUMBURG, P, LOVEDAY, C, BAJRAMI, I, BROUGH, R, RODRIGUES, D.N, RENWICK, A, SEAL, S, RAMSAY, E, DEL VECCHIO DUARTE, S, RIVAS, A. M, WARREN-PERRY, M, ZACHARIOU, A, CAMPION-FLORA, A, HANKS, S, MURRAY, A, POUR, N.A, DOUGLAS, J, GREGORY, J, RIMMER, A, WALKER, N.M, YANG, T-P, ADLARD, J.W, BARWELL, J, BERG, J, BRADY, A.F, BREWER, C, BRICE, G, CHAPMAN, C, COOK, J, DAVIDSON, R, DONALDSON, A, DOUGLAS, F, ECCLES, D, EVANS, D.G, GREENHALGH, L, HENDERSON, A, IZATT, L, KUMAR, A, LALLOO, F, MIEDZYBRODZKA, Z, MORRISON, P.J, PATERSON, J, PORTEOUS, M, ROGERS, M.T, SHANLEY, S, WALKER, L, GORE, M, HOULSTON, R, BROWN, M.A, CAUFIELD, M.J, DELOUKAS, P, MCCARTHY, M.I, TODD, J.A, the BREAST AND OVARIAN CANCER SUSCEPTIBILITY COLLABORATION,WELLCOME TRUST CASE CONTROL CONSORTIUM, TURNBULL, C, REIS-FILHO, J.S, ASHWORTH, A, ANTONIOU, A.C, LORD, C.J, DONNELLY, P and RAHMAN, N.  (2013)  Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer.  Nature, 493(7432),  406–410.

RUCKER, J.J.H, BREEN, G, PINTO, D, PEDROSO, I, LEWIS, C.M, COHEN-WOODS, S, UHER, R, SCHOSSER, A, RIVERA, M, AITCHISON, K.J, CRADDOCK, N, OWEN, M.J, JONES, L, JONES, I, KORSZUN, A, MUGLIA, P, BARNES, M.R, PREISIG, M, MORS, O, GILL, M, MAIER, W, RICE, J, RIETSCHEL, M, HOLSBOER, F, FARMER, A.E , CRAIG, W, SCHERER, S.W and McGUFFIN, P.  (2013)  Genome-wide association analysis of copy number variation in recurrent depressive disorder.  Molecular Psychiatry, 18(2),  183-189.