Prevalence of the LRRK2 G2019S mutation in a UK community based idiopathic Parkinson’s disease cohort von Williams-Gray, C H, Goris, A, Foltynie, T, Brown, J, Maranian, M, Walton, A, Compston, D A S, Sawcer, S J, Barker, R A

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Investigation of TGFB2 as a candidate gene in multiple sclerosis and Parkinson's disease von GORIS, A, WILLIAMS-GRAY, C. H, FOLTYNIE, T, BROWN, J, MARANIAN, M, WALTON, A, COMPSTON, D. A. S, BARKER, R. A, SAWCER, S. J

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A genome screen for linkage in Australian sibling-pairs with multiple sclerosis von Ban, M, Stewart, G J, Bennetts, B H, Heard, R, Simmons, R, Maranian, M, Compston, A, Sawcer, S J

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A High-Density Screen for Linkage in Multiple Sclerosis von Sawcer, Stephen, Ban, Maria, Maranian, Mel, Yeo, Tai Wai, Compston, Alastair, Kirby, Andrew, Daly, Mark J, De Jager, Philip L, Walsh, Emily, Lander, Eric S, Rioux, John D, Hafler, David A, Ivinson, Adrian, Rimmler, Jacqueline, Gregory, Simon G, Schmidt, Silke, Pericak-Vance, Margaret A, Akesson, Eva, Hillert, Jan, Datta, Pameli, Oturai, Annette, Ryder, Lars P, Harbo, Hanne F, Spurkland, Anne, Myhr, Kjell-Morten, Laaksonen, Mikko, Booth, David, Heard, Robert, Stewart, Graeme, Lincoln, Robin, Barcellos, Lisa F, Hauser, Stephen L, Oksenberg, Jorge R, Kenealy, Shannon J, Haines, Jonathan L

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Novel Olig1‐coding variants and susceptibility to multiple sclerosis von Goris, A, Yeo, T W, Maranian, M, Walton, A, Ban, M, Gray, J, Compston, A, Sawcer, S

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Crohn’s associated NOD2 gene variants are not involved in determining susceptibility to multiple sclerosis von Sawcer, S, Maranian, M, Hensiek, A, Roxburgh, R, Gray, J, Compston, A

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Fine scale mapping of the breast cancer 16q12 locus von Udler, Miriam S., Ahmed, Shahana, Healey, Catherine S., Meyer, Kerstin, Struewing, Jeffrey, Maranian, Melanie, Kwon, Erika M., Zhang, Jinghui, Tyrer, Jonathan, Karlins, Eric, Platte, Radka, Kalmyrzaev, Bolot, Dicks, Ed, Field, Helen, Maia, Ana-Teresa, Prathalingam, Radhika, Teschendorff, Andrew, McArthur, Stewart, Doody, David R., Luben, Robert, Caldas, Carlos, Bernstein, Leslie, Kolonel, Laurence K., Henderson, Brian E., Wu, Anna H., Le Marchand, Loic, Ursin, Giske, Press, Michael F., Lindblom, Annika, Margolin, Sara, Shen, Chen-Yang, Yang, Show-Lin, Hsiung, Chia-Ni, Kang, Daehee, Yoo, Keun-Young, Noh, Dong-Young, Ahn, Sei-Hyun, Malone, Kathleen E., Haiman, Christopher A., Pharoah, Paul D., Ponder, Bruce A.J., Ostrander, Elaine A., Easton, Douglas F., Dunning, Alison M.

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A genome wide linkage disequilibrium screen in Parkinson's disease von FOLTYNIE, Thomas, HICKS, Andrew, COMPSTON, Alastair, GULCHER, Jeff, BARKER, Roger A, SAWCER, Stephen, JONASDOTTIR, Aslaug, SETAKIS, Efrosini, MARANIAN, Melanie, YEO, Taiwai, LEWIS, Simon, BRAYNE, Carol, STEFANSSON, Kari

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Evidence for a Type 1 diabetes-specific mechanism for the insulin gene-associated IDDM2 locus rather than a general influence on autoimmunity von Tait, K. F., Collins, J. E., Heward, J. M., Eaves, I., Snook, H., Franklyn, J. A., Barnett, A. H., Todd, J. A., Maranian, M., Compston, A., Sawcer, S., Gough, S. C. L.

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A whole genome screen for linkage disequilibrium in multiple sclerosis confirms disease associations with regions previously linked to susceptibility von SAWCER, Stephen, MARANIAN, Mel, DEANS, Jackie, GOODFELLOW, Peter N, WALKER, Neil, CLAYTON, David, COMPSTON, Alastair, SETAKIS, Efrosini, CURWEN, Val, AKESSON, Eva, HENSIEK, Anke, CORADDU, Francesca, ROXBURGH, Richard, SAWCER, David, GRAY, Julia

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Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping von Sawcer, Stephen J, Maranian, Mel, Singlehurst, Sara, Yeo, TaiWai, Compston, Alastair, Daly, Mark J, De Jager, Philip L, Gabriel, Stacey, Hafler, David A, Ivinson, Adrian J, Lander, Eric S, Rioux, John D, Walsh, Emily, Gregory, Simon G, Schmidt, Silke, Pericak-Vance, Margaret A, Barcellos, Lisa, Hauser, Stephen L, Oksenberg, Jorge R, Kenealy, Shannon J, Haines, Jonathan L

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CD24 Ala/Val polymorphism and multiple sclerosis von Goris, An, Maranian, Melanie, Walton, Amie, Yeo, Tai Wai, Ban, Maria, Gray, Julia, Dubois, Bénédicte, Compston, Alastair, Sawcer, Stephen

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No evidence of a significant role for CTLA-4 in multiple sclerosis von Roxburgh, Richard H., Sawcer, Stephen, Maranian, Mel, Seaman, Shaun, Hensiek, Anke, Yeo, Taiwai, Deans, Jackie, Compston, Alastair

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Cytochrome P450 2D6 variants and their association with breast cancer survival von Abraham, JE, Maranian, M, Driver, K, Greenberg, D, Shah, MN, Earl, HM, Dunning, AM, Pharoah, PP, Caldas, C

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Feasibility and Construct Validity of PROMIS and “Legacy” Instruments in an Academic Scleroderma Clinic von Khanna, Dinesh, MD, MS, Maranian, Paul, MS, Rothrock, Nan, PhD, Cella, David, PhD, Gershon, Richard, PhD, Khanna, Puja P., MD, MPH, Spiegel, Brennan, MD, MSHS, Furst, Daniel E., MD, Clements, Phil J., MD, Bechtel, Amber, Hays, Ron D., PhD

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Four single nucleotide polymorphisms from the vitamin D receptor gene in UK multiple sclerosis von Yeo, Tai Wai, Maranian, Mel, Singlehurst, Sara, Gray, Julia, Compston, Alastair, Sawcer, Stephen

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SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosis von Fenoglio, Chiara, Galimberti, Daniela, Ban, Maria, Maranian, Mel, Scalabrini, Diego, Venturelli, Eliana, Piccio, Laura, De Riz, Milena, Yeo, Tai Wai, Goris, An, Gray, Julia, Bresolin, Nereo, Scarpini, Elio, Compston, Alastair, Sawcer, Stephen

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Novel Olig 1-coding variants and susceptibility to multiple sclerosis von Goris, A, Yeo, T W, Maranian, M, Walton, A, Ban, M, Gray, J, Compston, A, Sawcer, S

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Investigation of TGFB2 as a candidate gene in multiple sclerosis and Parkinson's disease von Goris, A, Williams-Gray, C.H, Foltynie, T, Brown, J, Maranian, M, Walton, A, Compston, D.A.S, Barker, R.A, Sawcer, S.J

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No alterations in α-synuclein gene dosage observed in sporadic Parkinson's disease von Williams-Gray, Caroline H., Goris, An, Foltynie, Thomas, Brown, Joanne, Maranian, Melanie, Walton, Amie, Compston, D. Alastair, Sawcer, Stephen J., Barker, Roger A.

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