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Issue Date
Title
Author(s)
2016
TBC1D24 genotype-phenotype correlation
Balestrini, S.
;
Milh, M.
;
Castiglioni, C.
;
Lüthy, K.
;
Finelli, M.
;
Verstreken, P.
;
Cardon, A.
;
Stražišar, B.
;
Holder, J.
;
Lesca, G.
;
Mancardi, M.
;
Poulat, A.
;
Repetto, G.
;
Banka, S.
;
Bilo, L.
;
Birkeland, L.
;
Bosch, F.
;
Brockmann, K.
;
Cross, J.
;
Doummar, D.
;
et al.
2015
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers
Onengut-Gumuscu, S.
;
Chen, W.-M.
;
Burren, O.
;
Cooper, N.J.
;
Quinlan, A.R.
;
Mychaleckyj, J.C.
;
Farber, E.
;
Bonnie, J.K.
;
Szpak, M.
;
Schofield, E.
;
Achuthan, P.
;
Guo, H.
;
Fortune, M.D.
;
Stevens, H.
;
Walker, N.M.
;
Ward, L.D.
;
Kundaje, A.
;
Kellis, M.
;
Daly, M.J.
;
Barrett, J.C.
;
et al.
2017
NAD deficiency, congenital malformations, and niacin supplementation
Shi, H.
;
Enriquez, A.
;
Rapadas, M.
;
Martin, E.
;
Wang, R.
;
Moreau, J.
;
Lim, C.
;
Szot, J.
;
Ip, E.
;
Hughes, J.
;
Sugimoto, K.
;
Humphreys, D.
;
McInerney-Leo, A.
;
Leo, P.
;
Maghzal, G.
;
Halliday, J.
;
Smith, J.
;
Colley, A.
;
Mark, P.
;
Collins, F.
;
et al.
2017
Dominant protection from HLA-linked autoimmunity by antigen-specific regulatory T cells
Ooi, J.
;
Petersen, J.
;
Tan, Y.
;
Huynh, M.
;
Willett, Z.
;
Ramarathinam, S.
;
Eggenhuizen, P.
;
Loh, K.
;
Watson, K.
;
Gan, P.
;
Alikhan, M.
;
Dudek, N.
;
Handel, A.
;
Hudson, B.
;
Fugger, L.
;
Power, D.
;
Holt, S.
;
Coates, P.
;
Gregersen, J.
;
Purcell, A.
;
et al.
2017
Electrophysiological, cognitive and clinical profiles of at-risk mental state: the longitudinal minds in transition (MinT) study
Atkinson, R.J.
;
Fulham, W.R.
;
Michie, P.T.
;
Ward, P.B.
;
Todd, J.
;
Stain, H.
;
Langdon, R.
;
Thienel, R.
;
Paulik, G.
;
Cooper, G.
;
Anthes, L.
;
Bowen, D.
;
Case, V.
;
Clark, S.
;
Collins-Langworthy, J.
;
Curtis, J.
;
Ehlkes, T.
;
Haddow, T.
;
Lawrence, C.
;
Logan, S.
;
et al.
;
Hashimoto, K.
2017
Epiregulin and EGFR interactions are involved in pain processing
Martin, L.J.
;
Smith, S.B.
;
Khoutorsky, A.
;
Magnussen, C.A.
;
Samoshkin, A.
;
Sorge, R.E.
;
Cho, C.
;
Yosefpour, N.
;
Sivaselvachandran, S.
;
Tohyama, S.
;
Cole, T.
;
Khuong, T.M.
;
Mir, E.
;
Gibson, D.G.
;
Wieskopf, J.S.
;
Sotocinal, S.G.
;
Austin, J.S.
;
Meloto, C.B.
;
Gitt, J.H.
;
Gkogkas, C.
;
et al.
2017
Antenatal suppression of il-1 protects against inflammation-induced fetal injury and improves neonatal and developmental outcomes in mice
Nadeau-Vallée, M.
;
Chin, P.
;
Belarbi, L.
;
Brien, M.
;
Pundir, S.
;
Berryer, M.
;
Beaudry-Richard, A.
;
Madaan, A.
;
Sharkey, D.
;
Lupien-Meilleur, A.
;
Hou, X.
;
Quiniou, C.
;
Beaulac, A.
;
Boufaied, I.
;
Boudreault, A.
;
Carbonaro, A.
;
Doan, N.
;
Joyal, J.
;
Lubell, W.
;
Olson, D.
;
et al.
2017
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
Geisheker, M.
;
Heymann, G.
;
Wang, T.
;
Coe, B.
;
Turner, T.
;
Stessman, H.
;
Hoekzema, K.
;
Kvarnung, M.
;
Shaw, M.
;
Friend, K.
;
Liebelt, J.
;
Barnett, C.
;
Thompson, E.
;
Haan, E.
;
Guo, H.
;
Anderlid, B.
;
Nordgren, A.
;
Lindstrand, A.
;
Vandeweyer, G.
;
Alberti, A.
;
et al.
2014
Inactivating mutations in NPC1L1 and protection from coronary heart disease
Stitziel, N.O.
;
Won, H.H.
;
Morrison, A.C.
;
Peloso, G.M.
;
Do, R.
;
Lange, L.A.
;
Fontanillas, P.
;
Gupta, N.
;
Duga, S.
;
Goel, A.
;
Farrall, M.
;
Saleheen, D.
;
Ferrario, P.
;
König, I.
;
Asselta, R.
;
Merlini, P.A.
;
Marziliano, N.
;
Notarangelo, M.F.
;
Schick, U.
;
Auer, P.
;
et al.
2014
Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing
Buchanan, D.
;
Tan, Y.
;
Walsh, M.
;
Clendenning, M.
;
Metcalf, A.
;
Ferguson, K.
;
Arnold, S.
;
Thompson, B.
;
Lose, F.
;
Parsons, M.
;
Walters, R.
;
Pearson, S.
;
Cummings, M.
;
Oehler, M.
;
Blomfield, P.
;
Quinn, M.
;
Kirk, J.
;
Stewart, C.
;
Obermair, A.
;
Young, J.
;
et al.
Discover
Author
11
Bloemenkamp, K.
10
Porath, M.
6
Gecz, J.
6
Kwee, A.
6
Papatsonis, D.
5
Choi, D.
5
Li, S.
5
Opmeer, B.
5
van Pampus, M.
5
Vos, T.
.
next >
Subject
158
Humans
122
Male
84
Adult
65
Middle Aged
51
Aged
38
Polymorphism, Single Nucleotide
32
Young Adult
30
Adolescent
27
Genetic Predisposition to Disease
27
Mutation
.
next >
Date issued
17
2017
17
2016
33
2015
13
2014
25
2013
18
2012
18
2011
18
2010