238 Publications (Page 8 of 10)
2012
Varenicline for smoking cessation: nausea severity and variation in nicotinic receptor genes
Swan, G. EJavitz, H. SJack, L. MWessel, J.Michel, M.Hinds, D. AStokowksi, R. PMcClure, J. BMcclure, J.B.Catz, S. LRichards, J.Zbikowski, S. MDeprey, M.McAfee, T.Mcafee, T.Conti, David and Bergen, A. W
Pharmacogenomics Journal, vol. 12, (no. 4), pp. 349-358, 2012. | Journal Article
2011
Environmental and genetic contributions to indicators of oral malodor in twins
Bretz, W.A.Biesbrock, A.Corby, P.M.Corby, A.L.Bretz, W.G.Wessel, J. and Schork, N.J.
Twin Research and Human Genetics, vol. 14, pp. 568-572. | Journal Article
 
Environmental and genetic contributions to indicators of oral malodor in twins.
Bretz, Walter ABiesbrock, AaronCorby, PatriciaCorby, Andrea LBretz, Walter GWessel, Jennifer and Schork, Nicholas J
Twin research and human genetics : the official journal of the International Society for Twin Studies, vol. 14, (no. 6), pp. 568-72, 2011/Dec. | Journal Article
 
Naturally occurring variations in the human cholinesterase genes: heritability and association with cardiovascular and metabolic traits.
Valle, Anne MRadi?, Z.Radic, ZoranRadić, Z.Rana, BrindaMahboubi, VafaWessel, JenniferShih, Pei-An BRao, FangwenO’Connor, D.T.O'connor, Daniel T and Taylor, Palmer W
The Journal of pharmacology and experimental therapeutics, vol. 338, (no. 1), pp. 125-33, 2011/Jul. | Journal Article
2010
Human tyrosine hydroxylase natural allelic variation: influence on autonomic function and hypertension.
Rao, FangwenZhang, KuixingZhang, LianRana, BrindaWessel, JenniferFung, Maple MRodriguez-Flores, Juan LTaupenot, LaurentZiegler, Michael GOConnor, D.T. and O'connor, Daniel T
Cellular and molecular neurobiology, vol. 30, (no. 8), pp. 1391-4, 2010/Nov. | Journal Article
 
Presymptomatic risk assessment for chronic non-communicable diseases.
Padhukasahasram, BadriHalperin, EranWessel, JenniferThomas, Daryl JSilver, ElanaTrumbower, HeatherCargill, Michele and Stephan, Dietrich A
PloS one, vol. 5, (no. 12), pp. e14338, 2010. | Journal Article
 
Resequencing of nicotinic acetylcholine receptor genes and association of common and rare variants with the Fagerström test for nicotine dependence
Wessel, J.McDonald, S.M.Hinds, D.A.Stokowski, R.P.Javitz, H.S.Kennemer, M.Krasnow, R.Dirks, W.Hardin, J.Pitts, S.J.Michel, M.Jack, L.Ballinger, D.G.McClure, J.B.Swan, G.E. and Bergen, A.W.
Neuropsychopharmacology, vol. 35, pp. 2392-2402. | Journal Article
2009
CACNA1C gene polymorphisms, cardiovascular disease outcomes, and treatment response.
Beitelshees, AmberNavare, HrishikeshWang, DanxinGong, YanWessel, JenniferMoss, James ILangaee, Taimour YCooper-DeHoff, R.M.Cooper Dehoff, Rhonda MSadee, WolfgangPepine, Carl JSchork, Nicolas J and Johnson, Julie A
Circulation. Cardiovascular genetics, vol. 2, (no. 4), pp. 362-70, 2009/Aug. | Journal Article
 
Methods and Systems for Incorporating Multiple Environmental and Genetic Risk Factors
Halperin, EranWessel, JenniferCargill, Michele and Stephan, Dietrich A
 
Natural variation within the neuronal nicotinic acetylcholine receptor cluster on human chromosome 15q24: influence on heritable autonomic traits in twin pairs.
Rana, BrindaWessel, JenniferMahboubi, VafaRao, FangwenHaeller, JeannineGayen, Jiaur REskin, EleazarValle, Anne MDas, MadhusudanMahata, Sushil KTaupenot, LaurentStridsberg, MatsTalley, Todd TZiegler, Michael GSmith, Douglas WSchork, Nicholas JO’Connor, D.T.O'connor, Daniel T and Taylor, Palmer W
The Journal of pharmacology and experimental therapeutics, vol. 331, (no. 2), pp. 419-28, 2009/Nov. | Journal Article
 
Nicotine withdrawal sensitivity, linkage to chr6q26, and association of OPRM1 SNPs in the SMOking in FAMilies (SMOFAM) sample
Hardin, J.He, Y.Javitz, H.S.Wessel, J.Krasnow, R.E.Tildesley, E.Hops, H.Swan, G.E. and Bergen, A.W.
Cancer Epidemiology Biomarkers and Prevention, vol. 18, pp. 3399-3406. | Journal Article
2008
Adrenergic Polymorphism and the Human Stress Response
Rao, FangwenRao, FangwenZhang, LianZhang, LianWessel, JenniferWessel, JenniferZhang, KuixingZhang, KuixingWen, GenWen, GenKennedy, Brian PKennedy, BrianRana, BrindaRana, BrindaDas, MadhusudanDas, MadhusudanRodriguez-Flores, JuanRodriguez-Flores, Juan LSmith, Douglas WSmith, DouglasCadman, PeterCadman, Peter ESalem, RanySalem, Rany MMahata, Sushil KumarMahata, SushilSchork, Nicholas JSchork, NicholasTaupenot, LaurentTaupenot, LaurentZiegler, MichaelZiegler, MichaelO’Connor, D.T.O'Connor, Daniel and O'connor, Daniel
Annals of the New York Academy of Sciences, vol. 1148, pp. 282-296, 2008. | Journal Article
 
DNA Sequence-Based Phenotypic Association Analysis
Schork, N.J.Wessel, J. and Malo, N.
2008
 
Evidence for a heritable unidimensional symptom factor underlying obsessionality
Mathews, Carol AMathew, Carol A.Greenwood, TiffanyWessel, JenniferAzzam, AminGarrido, HelenaChavira, DeniseChandavarkar, UmaBagnarello, MonicaStein, Murray and Schork, Nicholas J
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, vol. 147B, (no. 6), pp. 676-685, 2008. | Journal Article
 
Evidence for a heritable unidimensional symptom factor underlying obsessionality.
Mathew, Carol A.Mathews, Carol AGreenwood, TiffanyGreenwood, TiffanyWessel, JenniferWessel, JenniferAzzam, AminAzzam, AminGarrido, HelenaGarrido, HelenaChavira, DeniseChavira, Denise A.Chandavarkar, UmaChandavarkar, UmaBagnarello, MonicaBagnarello, MonicaStein, MurrayStein, MurraySchork, Nicholas J and Schork, Nicholas J.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, vol. 147B, (no. 6), pp. 676-85, 2008/Sep/5. | Journal Article
 
Inheritance of occlusal topography: a twin study.
Su, C-YCorby, PatriciaElliot, M AStuden-Pavlovich, D ARanalli, Dennis NRosa, BWessel, JSchork, N JHart, Thomas C and Bretz, Walter A
European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry, vol. 9, (no. 1), pp. 19-24, 2008/Mar. | Journal Article
 
Inheritance of occlusal topography: a twin study.
Su, C.Y.Corby, P.M.Elliot, M.A.Studen-Pavlovich, D.A.Ranalli, D.N.Rosa, B.Wessel, J.Schork, N.J.Hart, T.C. and Bretz, W.A.
(pp. 19-24)
 
Investigating naturally occurring variations in the Acetylcholinesterase gene of a human population
Valle, Anne MarieRadic, ZoranHo, Kwok-YiuMahboubi, VafaWessel, JenniferRao, FangwenRana, Brinda KO'Connor, Daniel TO’Connor, Daniel T and Taylor, Palmer
The FASEB Journal, vol. 22, pp. 1134--2. FASEB. | Conference Proceeding
 
Investigating naturally occurring variations in the Acetylcholinesterase gene of a human population
Valle, Anne MarieRadic, ZoranHo, Kwok-YiuMahboubi, VafaWessel, JenniferRao, FangwenRana, Brinda KO’Connor, Daniel T and Taylor, Palmer
(pp. 1134–2). FASEB
 
Methods and Systems for Genomic Analysis Using Ancestral Data
Stephan, Dietrich AWessel, JenniferCargill, Michele and Halperin, Eran
2007
Accommodating pathway information in expression quantitative trait locus analysis
Wessel, J.Zapala, MA and Schork, Nicholas J
Genomics, vol. 90, (no. 1), pp. 132-142, 2007. | Journal Article
 
An ancestral variant of Secretogranin II confers regulation by PHOX2 transcription factors and association with hypertension
Wen, GenWessel, JenniferZhou, WeidongEhret, Georg BRao, FangwenStridsberg, MatsMahata, Sushil KumarGent, Peter MDas, MadhusudanCooper, Richard SChakravarti, AravindaZhou, HuilinSchork, Nicholas JO'connor, DanielO’Connor, D.T. and Hamilton, Bruce A
Human Molecular Genetics, vol. 16, (no. 14), pp. 1752-1764, 2007. | Journal Article
 
C-reactive protein, an 'intermediate phenotype' for inflammation: human twin studies reveal heritability, association with blood pressure and the metabolic syndrome, and the influence of common polymorphism at catecholaminergic/beta-adrenergic pathway loci.
Wessel, JenniferMoratorio, GuillermoRao, FangwenMahata, ManjulaZhang, LianGreene, WilliamRana, BrindaKennedy, Brian PKhandrika, SrikrishnaHuang, PaulineLillie, Elizabeth OShih, Pei-An BSmith, Douglas WWen, GenHamilton, Bruce AZiegler, Michael GWitztum, Joseph LSchork, Nicholas JSchmid Schoenbein, Geert WSchmid-Schönbein, Geert W and O'connor, Daniel T
Journal of hypertension, vol. 25, (no. 2), pp. 329-43, 2007/Feb. | Journal Article
 
C-reactive protein, an 'intermediate phenotype' for inflammation: Human twin studies reveal heritability, association with blood pressure and the metabolic syndrome, and the influence of common polymorphism at catecholaminergic/β-adrenergic pathway loci
Wessel, JenniferWessel, J.Moratorio, GuillermoMoratorio, G.Rao, F.Rao, FangwenMahata, ManjulaMahata, M.Zhang, L.Zhang, LianGreene, W.Greene, WilliamRana, BrindaRana, B.K.Kennedy, B.P.Kennedy, BrianKhandrika, S.Khandrika, SrikrishnaHuang, P.Huang, PaulineLillie, E.O.Lillie, ElizabethShih, P.-A.B.Shih, Pei-AnSmith, D.W.Smith, DouglasWen, G.Wen, GenHamilton, BruceHamilton, B.A.Ziegler, M.G.Ziegler, MichaelWitztum, J.L.Witztum, JosephSchork, NicholasSchork, N.J.Schmid-Schönbein, G.W.Schmid-Schönbein, GeertO’Connor, D.T.OʼConnor, Daniel and O'Connor, D.T.
Journal of Hypertension, vol. 25, pp. 329-343. | Journal Article
 
Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk.
Zhang, LianRao, FangwenZhang, KuixingKhandrika, SrikrishnaDas, MadhusudanVaingankar, Sucheta MBao, XupingRana, BrindaSmith, Douglas WWessel, JenniferSalem, Rany MRodriguez-Flores, Juan LMahata, Sushil KSchork, Nicholas JZiegler, Michael GO'connor, Daniel T and O’Connor, D.T.
The Journal of clinical investigation, vol. 117, (no. 9), pp. 2658-71, 2007/Sep. | Journal Article