Bibliography

SALEH, N.M, RAJ, S.M, SMYTH, D.J, WALLACE, C, HOWSON, J.M, BELL, L, WALKER, N.M, STEVENS, H.E and TODD, J.A.  (2011)  Genetic association analyses of atopic illness and proinflammatory cytokine geneswith type 1 diabetes.  Diabetes/Metabolism Research Reviews, 27(8),  838-843.

SALEM, A.H, FARID, E, FADEL, R, ABU-HIJLEH, M, ALMAWI, W, HAN, K and BATZER, M.A.  (2009)  Distribution of four hiv type 1-resistance polymorphisms (ccr5-delta32, ccr5-m303, ccr2-64i, and sdf1-3'a) in the Bahraini population.  AIDS Research & Human Retroviruses, 25(10),  973-977.

SALMELA, E, LAPPALAINEN, T, FRANSSON, I, ANDERSEN, P.M, DAHLMAN-WRIGHT, K, FIEBIG, A, SISTONEN, P, SAVONTAUS, M.L, SCHREIBER, S, KERE, J and LAHERMO, P.  (2008)  Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe.  PLoS One, 3(10),  e3519.

SALMELA, E, LAPPALAINEN, T, LIU, J, SISTONEN, P, ANDERSEN, P.M, SCHREIBER, S, SAVONTAUS, M.L, CZENE, K, LAHERMO, P, HALL, P and KERE, J.  (2011)  Swedish population substructure revealed by genome-wide single nucleotide polymorphism data.  PLoS One, 6(2),  e16747.

SALMELA-ARO, K and SCHOON, I.  (2005)  Human Development and Well-Being.  European Psychologist, 10(4),  259-263.

SAMAD, L, TATE, A.R, DEZATEUX, C, PECKHAM, C, BUTLER, N and BEDFORD, H.  (2006)  Differences in risk factors for partial and no immunisation in the first year of life: prospective cohort study.  British Medical Journal, 332, 1312-1313.

SAMANI, N.J, ERDMANN, J, HALL, A.S, HENGSTENBERG, C, MANGINO, M, MAYER, B, DIXON, R.J, MEITINGER, T, BRAUND, P, WICHMANN, H-E, BARRETT, J.H, KÖNIG, I.R, STEVENS, S.E, SZYMCZAK, S, TREGOUET, D-A, ILES, M.M, PAHLKE, F, POLLARD, H, LIEB, W, CAMBIEN, F, FISCHER, M, OUWEHAND, W, BLANKENBERG, S, BALMFORTH, A.J, BAESSLER, A, BALL, S.G, STROM, T.M, BRÆNNE, I, GIEGER, C, DELOUKAS, P, TOBIN, M.D, ZIEGLER, A, THOMPSON, J.R, SCHUNKERT, H, WTCCC and the CARDIOGENICS CONSORTIUM.  (2007)  Genomewide Association Analysis of Coronary Artery Disease.  New England Journal of Medicine, 357(5),  443-453.

SAMEK, L., DARKO, C., KING, W., SIDHU, S.V., PARMAR, M., FOLIANO, F., MOORE, J., O'MAHONY, M., PAYNE, C., RINCON-AZNAR, A. and VASSILEV, G.  (2019)  Provision of Human Capital Evidence Review.  A Report for the Office for National Statistics. London: National Institute of Economic and Social Research.

SANDHU, M.S, WATERWORTH, D.M, DEBENHAM, S.L, WHEELER, E, PAPADAKIS, K, ZHAO, J.H, SONG, K, YUAN, X, JOHNSON, T, ASHFORD, S, INOUYE, M, LUBEN, R, SIMS, M, HADLEY, D, McARDLE, W, BARTER, P, KESANIEMI, Y.A, MAHLEY, R.W, McPHERSON, R, GRUNDY, S.M, BINGHAM, S.A, KHAW, K.T, LOOS, R.J, WAEBER, G, BARROSO, I, STRACHAN, D.P, DELOUKAS, P, VOLLENWEIDER, P, WAREHAM, N.J and MOOSER, V.  (2008)  LDL-cholesterol concentrations: a genome-wide association study.  Lancet, 371(9611),  483-491.

SANDHU, M.S, WEEDON, M.N, FAWCETT, K.A, WASSON, J, DEBENHAM, S.L, DALY, A, LANGO, H, FRAYLING, T.M, NEUMANN, R.J, SHERVA, R, BLECH, I, PHAROAH, P.D, PALMER, C.N.A, KIMBER, C, TAVENDALE, R, MORRIS, A.D, McCARTHY, M.I, WALKER, M, HITMAN, G, GLASER, B, PERMUTT, M.A, HATTERSLEY, A.T, WAREHAM, N.J and BARROSO, I.  (2007)  Common variants in WFS1 confer risk of type 2 diabetes.  Nature Genetics, 39(8),  951-953.

SANDILANDS, J.  (1976)  Portrait of a generation - how sweet is 16?  Observer Colour Magazine,12 September 1976. pp14-23.

SANGKET, U, MAHASIRIMONGKOL, S, TANDAYYA, P, SANGKHATHAT, S, CHANTRATITA, W, LIU, Q and YASUI, Y.  (2017)  Parallelization of Logic Regression Analysis on SNP-SNP Interactions of a Crohn’s Disease Dataset Model.  Sains Malaysiana, 46(9),  1449-1455.

SANJAK, J.S, LONG, A.D and THORNTON, K.R.  (2016)  Efficient Software for Multi-marker, Region-Based Analysis of GWAS Data.  G3: Genes | Genomes | Genetics, 6 (4),  1023-1030.

SANNA, S, JACKSON, A.U, NAGARAJA, R, WILLER, C.J, CHEN, W.M, BONNYCASTLE, L.L, SHEN, H, TIMPSON, N, LETTRE, G, USALA, G, CHINES, P.S, STRINGHAM, H.M, SCOTT, L.J, DEI, M, LAI, S, ALBAI, G, CRISPONI, L, NAITZA, S, DOHENY, K.F, PUGH, E.W, BEN-SHLOMO, Y, EBRAHIM, S, LAWLOR, D.A, BERGMAN, R.N, WATANABE, R.M, UDA, M, TUOMILEHTO, J, CORESH, J, HIRSCHHORN, J.N, SHULDINER, A.R, SCHLESSINGER, D, COLLINS, F.S, DAVEY SMITH, G, BOERWINKLE, E, CAO, A, BOEHNKE, M, ABECASIS, G.R and MOHLKE, K.L.  (2008)  Common variants in the GDF5-UQCC region are associated with variation in human height.  Nature Genetics, 40(2),  198-203.

SANNER, C. and JENSEN, T. M.  (2021)  Toward more accurate measures of family structure: Accounting for sibling complexity.  Journal of Family Theory & Review, 13(1),  110-127.

SANNERUD, J.  (2023)  Sex and the X: Developing Sex-Specific Pedigree Inference and Evaluating X Chromosome Identity by Descent.  Doctoral Thesis.Cornell University.

SANSON, M, HOSKING, F.J, SHETE, S, ZELENIKA D, DOBBINS SE, MA Y, ENCISO-MORA V, IDBAIH A, DELATTRE JY, HOANG-XUAN K, MARIE Y, BOISSELIER B, CARPENTIER C, WANG XW, DI STEFANO AL, LABUSSIÈRE M, GOUSIAS K, SCHRAMM J, BOLAND A, LECHNER D, GUT I, ARMSTRONG G, LIU Y, YU R, LAU C, DI BERNARDO MC, ROBERTSON LB, MUIR K, HEPWORTH S, SWERDLOW A, SCHOEMAKER MJ, WICHMANN HE, MÜLLER M, SCHREIBER S, FRANKE A, MOEBUS S, EISELE L, FÖRSTI A, HEMMINKI K, LATHROP M, BONDY, M, HOULSTON, R.S and SIMON M.  (2011)  Chromosome 7p11.2 (EGFR) variation influences glioma risk.  Human Molecular Genetics, 20(14),  2897-2904.

SANTORSOLA, M and LESCAI, F.  (2023)  The promise of explainable deep learning for omics data analysis: Adding new discovery tools to AI.  New Biotechnology, 77(45255),  45231.

SASSLER, S, ADDO, F.R, PERELLI-HARRIS, B, LAPPEGåRD and HOHERZ, S.  (2023)  Partnered, Cohabiting, or Married: Childbearing and Mothers' Mid-Life Health in the US, UK, and Norway.  In BLAIR, S.L and ZHANG, Y (ed), Cohabitation and the Evolving Nature of Intimate and Family Relationships, Volume 24. Leeds: Emerald Publishing.

SAUNDERS, P.  (1997)  Social Mobility in Britain: An Empirical Evaluation of Two Competing Explanations.  Sociology, 31(2),  261-288.