648 Publications (Page 21 of 26)
2005
Genetic screening for a single common LRRK2 mutation in familial Parkinson's diseaseNichols, William C⋅Nichols, William C⋅Pankratz, Nathan⋅Pankratz, Nathan⋅Hernandez, Dena⋅Hernandez, Dena⋅Paisán-Ruíz, Coro⋅Paisán-Ruíz, Coro⋅al, et⋅Jain, Shushant⋅Halter, Cheryl A⋅Michaels, Veronika E⋅Reed, Terry⋅Rudolph, Alice⋅Shults, Clifford W⋅Singleton, Andrew and Foroud, TatianaThe Lancet, vol. 365, (no. 9457), pp. 412, 2005.
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Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease.Nichols, William C⋅Pankratz, Nathan⋅Hernandez, Dena⋅Paisán-Ruíz, Coro⋅Jain, Shushant⋅Halter, Cheryl A⋅Michaels, Veronika E⋅Reed, Terry E⋅Rudolph, Alice⋅Shults, Clifford W⋅Singleton, Andrew and Foroud, Tatiana MLancet. , vol. 365, (no. 9457), pp. 410-2, 2005 Jan 29-Feb 4.
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Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease.(Research Letters)(leucine-rich repeat kinase 2Singleton, Andrew⋅Shults, Clifford⋅Pankratz, Nathan⋅Halter, Cheryl⋅Rudolph, Alice⋅Nichols, William⋅Jain, Shushant⋅Paisan-Ruiz, Coro⋅Hernandez, Dena⋅Michaels, Veronika⋅Reed, Terry⋅Singleton, Andrew⋅Shults, Clifford⋅Foroud, Tatiana⋅Pankratz, Nathan⋅Halter, Cheryl⋅Rudolph, Alice⋅Jain, Shushant⋅Paisan-Ruiz, Coro⋅Hernandez, Dena⋅Michaels, Veronika⋅Reed, Terry⋅Foroud, Tatiana and Nichols, WilliamThe Lancet, vol. 365, (no. 9457), pp. 410, 20050129.
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Genome screen for bone mineral density phenotypes in Fisher 344 and Lewis rat strainsKoller, Daniel⋅Alam, Imranul⋅Sun, Qiwei⋅Liu, Lixiang⋅Fishburn, Tonya⋅Carr, Lucinda G⋅Econs, Michael⋅Foroud, Tatiana M and Turner, Charles HMammalian Genome, vol. 16, (no. 8), pp. 578-586, 2005.
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LRRK2: Both a cause and a risk factor for Parkinson disease?Foroud, TatianaNeurology, vol. 65, (no. 5), pp. 665, 2005-Sep-13.
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No association of the GABAA receptor genes on chromosome 5 with alcoholism in the collaborative study on the genetics of alcoholism sample.Dick, Danielle M⋅Edenberg, Howard J⋅Xuei, Xiaoling⋅Goate, Alison⋅Hesselbrock, Victor M⋅Schuckit, Marc⋅Crowe, Raymond and Foroud, Tatiana MAmerican journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, vol. 132, (no. 1), pp. 24-8, 2005/Jan/5.
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No association of the GABA sub(A) receptor genes on chromosome 5 with alcoholism in the collaborative study on the genetics of alcoholism sampleDick, Danielle Marie⋅Dick, Danielle M⋅Edenberg, Howard J⋅Edenberg, Howard J⋅Xuei, Xiaoling⋅Xuei, Xiaoling⋅Goate, Alison⋅Goate, Alison⋅Hesselbrock, Victor⋅Hesselbrock, Victor⋅Schuckit, Marc⋅Schuckit, Marc⋅Crowe, Raymond⋅Crowe, Raymond⋅Foroud, Tatiana and Foroud, Tatiana MAmerican Journal of Medical Genetics B, vol. 132B, (no. 1), pp. 24-28, 2005.
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Polymorphisms in the estrogen receptor beta (ESR2) gene are associated with bone mineral density in Caucasian men and women.Ichikawa, Shoji⋅Koller, Daniel L⋅Peacock, Munro⋅Johnson, Michelle L⋅Lai, Dongbing⋅Hui, Siu L⋅Johnston, C C⋅Foroud, Tatiana M and Econs, Michael JThe Journal of clinical endocrinology and metabolism, vol. 90, (no. 11), pp. 5921-7, 2005/Nov.
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Polymorphisms in the Estrogen Receptor {szligbeta} (ESR2) Gene Are Associated with Bone Mineral Density in Caucasian Men and WomenIchikawa, Shoji⋅Koller, Daniel⋅Peacock, Munro⋅Johnson, Michelle L⋅Lai, Dongbing⋅Hui, Siu L⋅Johnston, CConrad⋅Foroud, Tatiana M and Econs, MichaelJournal of Clinical Endocrinology and Metabolism, vol. 90, (no. 11), pp. 5921-5927, 2005.
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Polymorphisms in the Estrogen Receptor β (ESR2) Gene Are Associated with Bone Mineral Density in Caucasian Men and WomenIchikawa, Shoji⋅Ichikawa, Shoji⋅Ichikawa, Shoji⋅Koller, Daniel L⋅Koller, Daniel L⋅Koller, Daniel L⋅Peacock, Munro⋅Peacock, Munro⋅Peacock, Munro⋅Johnson, Michelle L⋅Johnson, Michelle L⋅Johnson, Michelle L⋅Lai, Dongbing⋅Lai, Dongbing⋅Lai, Dongbing⋅Hui, Siu L⋅Hui, Siu L⋅Hui, Siu L⋅Johnston, C. Conrad⋅Johnston, C. Conrad⋅Johnston, C. Conrad⋅Foroud, Tatiana M⋅Foroud, Tatiana M⋅Foroud, Tatiana M⋅Econs, Michael J⋅Econs, Michael J and Econs, Michael JThe Journal of Clinical Endocrinology & Metabolism, vol. 90, (no. 11), pp. 5927, 2005-11.
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Sex-Specific and Non-Sex-Specific Quantitative Trait Loci Contribute to Normal Variation in Bone Mineral Density in MenPeacock, Munro⋅Koller, Daniel⋅Fishburn, Tonya⋅Krishnan, Subha⋅Lai, Dongbing⋅Hui, Siu L⋅Johnston, CConrad⋅Foroud, Tatiana M and Econs, MichaelJournal of Clinical Endocrinology and Metabolism, vol. 90, (no. 5), pp. 3060-3066, 2005.
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Sex-specific quantitative trait loci contribute to normal variation in bone structure at the proximal femur in menPeacock, Munro⋅Koller, Daniel⋅Lai, D.⋅Hui, Siu L⋅Foroud, Tatiana M and Econs, MichaelBone, vol. 37, (no. 4), pp. 467-473, 2005.
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Standard linkage and association methods identify the mechanism of four susceptibility genes for a simulated complex diseasePankratz, Nathan⋅Edenberg, Ellen and Foroud, TatianaBMC genetics, vol. 6 Suppl 1, (no. Suppl 1), pp. S142, 2005-Dec-30.
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The Familial Intracranial Aneurysm (FIA) study protocolBroderick, Joseph P⋅Broderick, Joseph P⋅Sauerbeck, Laura⋅Sauerbeck, Laura R⋅Foroud, Tatiana⋅Foroud, Tatiana⋅Huston, 3rd, John⋅Huston III, John⋅Pankratz, Nathan⋅Pankratz, Nathan⋅Meissner, Irene⋅Meissner, Irene⋅Brown, Jr, Robert D and Brown, Robert DBMC medical genetics, vol. 6, (no. 1), pp. 17, 2005-Apr-26.
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The North American Multiple System Atrophy Study GroupGilman, Sid⋅May, Susanne⋅Shults, Clifford W⋅Tanner, Caroline⋅Kukull, Walter A⋅Lee, Virginia M⋅Masliah, Eliezer⋅Low, Phillip A⋅Sandroni, P.⋅Trojanowski, John Q⋅Ozelius, Laurie and Foroud, Tatiana MJournal of Neural Transmission, vol. 112, (no. 12), pp. 1687-1694, Dec 2005.
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Whole-Genome Scan for Linkage to Bone Strength and Structure in Inbred Fischer 344 and Lewis RatsAlam, Imranul⋅Sun, Qi⋅Liu, L.⋅Koller, Daniel⋅Fishburn, T.⋅Carr, Lucinda G⋅Econs, Michael⋅Foroud, Tatiana M and Turner, Charles HJournal of Bone and Mineral Research, vol. 20, (no. 9), pp. 1589-1596, 2005.
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2004
A genome-wide screen for genes influencing conduct disorderDick, Danielle M⋅Li, T-K⋅Edenberg, Howard J⋅Hesselbrock, Victor M⋅Kramer, J.⋅Kuperman, Samuel⋅Porjesz, B.⋅Bucholz, Kathleen K⋅Goate, Alison⋅Nurnberger, John I⋅Nurnberger Jr., J. and Foroud, Tatiana MMolecular Psychiatry, vol. 9, (no. 1), pp. 81-86, 2004.
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A genomic scan for habitual smoking in families of alcoholics: common and specific genetic factors in substance dependence.Bierut, Laura J⋅Bierut, Laura Jean⋅Rice, John P⋅Rice, John P⋅Goate, Alison⋅Goate, Alison⋅Hinrichs, Tony⋅Hinrichs, Anthony L⋅Saccone, Nancy L⋅Saccone, Nancy L⋅Foroud, Tatiana⋅Foroud, Tatiana⋅Edenberg, Howard J⋅Edenberg, Howard J⋅Cloninger, C Robert⋅Cloninger, C. R⋅Begleiter, Henri⋅Begleiter, Henri⋅Conneally, P Michael⋅Conneally, P M⋅Crowe, Raymond R⋅Crowe, Raymond R⋅Hesselbrock, Victor M⋅Hesselbrock, Victor⋅Li, Ting-Kai⋅Li, Ting-Kai⋅Nurnberger, John I⋅Nurnberger, John I⋅Porjesz, Bernice⋅Porjesz, Bernice⋅Schuckit, Marc A⋅Schuckit, Marc A⋅Reich, Theodore and Reich, TheodoreAmerican journal of medical genetics. Part A, vol. 124A, (no. 1), pp. 19-27, January 1, 2004.
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A genomic scan for habitual smoking in families of alcoholics: Common and specific genetic factors in substance dependenceBierut, Laura J⋅Bierut, Laura Jean⋅Bierut, Laura Jean⋅Rice, JP⋅Rice, John P⋅Rice, John P⋅Goate, Alison⋅Goate, Alison⋅Goate, A.⋅Hinrichs, Tony⋅Hinrichs, Anthony L⋅Hinrichs, Anthony L⋅Saccone, Nancy L⋅Saccone, Nancy L⋅Saccone, Nancy L⋅Foroud, Tatiana⋅Foroud, Tatiana⋅Foroud, T.⋅Edenberg, Howard J⋅Edenberg, Howard J⋅Edenberg, Howard J⋅Cloninger, C. R⋅Cloninger, C. Robert⋅Cloninger, C. Robert⋅Begleiter, Henri⋅Begleiter, H.⋅Begleiter, Henri⋅Conneally, PM⋅Conneally, P. Michael⋅Conneally, P. Michael⋅Crowe, Raymond R⋅Crowe, Raymond R⋅Crowe, RR⋅Hesselbrock, Victor⋅Hesselbrock, Victor⋅Hesselbrock, Victor M⋅Li, Ting‐Kai⋅Li, Ting‐Kai⋅Li, T-K⋅Nurnberger, John I⋅Nurnberger, John I⋅Nurnberger, John I⋅Porjesz, Bernice⋅Porjesz, Bernice⋅Porjesz, B.⋅Schuckit, Marc A⋅Schuckit, Marc A⋅Schuckit, Marc A⋅Reich, Theodore⋅Reich, T. and Reich, TheodoreAmerican Journal of Medical Genetics Part A, vol. 124A, (no. 1), pp. 27, 1 January 2004.
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Association of GABRG3 With Alcohol DependenceDick, Danielle M⋅Dick, Danielle M⋅Edenberg, Howard J⋅Edenberg, Howard J⋅Xuei, Xiaoling⋅Xuei, Xiaoling⋅Goate, Alison⋅Goate, Alison⋅Kuperman, Sam⋅Kuperman, Sam⋅Schuckit, Marc A⋅Schuckit, Marc⋅Crowe, Raymond⋅Crowe, Raymond⋅Smith, Tom L⋅Smith, Tom L⋅Porjesz, Bernice⋅Porjesz, Bernice⋅Begleiter, Henri⋅Begleiter, Henri⋅Foroud, Tatiana and Foroud, TatianaAlcoholism: Clinical and Experimental Research, vol. 28, (no. 1), pp. 9, January 2004.
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Confirmation of Linkage to Chromosome 1q for Peak Vertebral Bone Mineral Density in Premenopausal White WomenEcons, Michael⋅Koller, Daniel⋅Hui, Siu L⋅Fishburn, T.⋅Conneally, P. M⋅Johnston, CC J⋅Peacock, Munro and Foroud, Tatiana MAmerican Journal of Human Genetics, vol. 74, (no. 2), pp. 223-228, 2004.
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Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease.Nichols, W.C.⋅Nichols, William C⋅Nichols, W.C.⋅Uniacke, Sean K⋅Uniacke, S.K.⋅Uniacke, S.K.⋅Pankratz, N.⋅Pankratz, N.⋅Pankratz, Nathan⋅Reed, T.⋅Reed, Terry E⋅Reed, T.⋅Simon, D.K.⋅Simon, D.K.⋅Simon, David K⋅Halter, C.⋅Halter, C.⋅Halter, Cheryl⋅Rudolph, A.⋅Rudolph, Alice⋅Rudolph, A.⋅Shults, C.W.⋅Shults, Clifford W⋅Shults, C.W.⋅Conneally, P.M.⋅Conneally, P. M⋅Conneally, P.M.⋅Foroud, Tatiana M⋅Foroud, T.⋅Foroud, T.⋅Wojcieszek, J.⋅Wojcieszek, J.⋅Belden, J.⋅Belden, J.⋅Carter, J.⋅Carter, J.⋅Camicioli, R.⋅Camicioli, R.⋅Andrews, P.⋅Andrews, P.⋅Panisset, M.⋅Panisset, M.⋅Hall, J.⋅Hall, J.⋅Hubble, J.⋅Hubble, J.⋅Fernandez, M.⋅Fernandez, M.⋅Reider, C.⋅Reider, C.⋅Rajput, A.⋅Rajput, A.⋅Rajput, A.⋅Rajput, A.⋅Shirley, T.⋅Shirley, T.⋅Mendis, T.⋅Mendis, T.⋅Grimes, D.A.⋅Grimes, D.A.⋅Gray, P.⋅Gray, P.⋅Ramos, C.S.⋅Ramos, C.S.⋅Roque, S.⋅Roque, S.⋅Pfeiffer, R.⋅Pfeiffer, R.⋅Pfeiffer, B.⋅Pfeiffer, B.⋅Elmer, L.⋅Elmer, L.⋅Davis, K.⋅Davis, K.⋅Friedman, J.⋅Friedman, J.⋅Fernandez, H.⋅Fernandez, H.⋅Lannon, M.⋅Lannon, M.⋅Reich, S.⋅Reich, S.⋅Dunlop, B.⋅Dunlop, B.⋅Seeberger, L.⋅Seeberger, L.⋅O’Brien, C.⋅O’Brien, C.⋅Judd, D.⋅Judd, D.⋅Hauser, R.⋅Hauser, R.⋅Zesiewicz, T.⋅Zesiewicz, T.⋅Delgado, H.⋅Delgado, H.⋅Shults, C.⋅Shults, C.⋅Fontaine, D.⋅Fontaine, D.⋅Jennings, D.⋅Jennings, D.⋅Marek, K.⋅Marek, K.⋅Mendick, S.⋅Mendick, S.⋅Aminoff, M.⋅Aminoff, M.⋅DiMinno, M.⋅DiMinno, M.⋅Lewitt, P.⋅Lewitt, P.⋅DeAngelis, M.⋅DeAngelis, M.⋅Pahwa, R.⋅Pahwa, R.⋅Thomas, S.⋅Thomas, S.⋅Truong, D.⋅Truong, D.⋅Pathak, M.⋅Pathak, M.⋅Tran, A.⋅Tran, A.⋅Rodnitzky, R.⋅Rodnitzky, R.⋅Dobson, J.⋅Dobson, J.⋅Koller, W.⋅Koller, W.⋅Weiner, W.⋅Weiner, W.⋅Lyons, K.⋅Lyons, K.⋅Kurlan, R.⋅Kurlan, R.⋅Berry, D.⋅Berry, D.⋅Bertoni, J.⋅Bertoni, J.⋅Peterson, C.⋅Peterson, C.⋅Martin, W.⋅Martin, W.⋅Tuite, P.⋅Tuite, P.⋅Schacherer, R.⋅Schacherer, R.⋅Marder, K.⋅Marder, K.⋅Harris, J.⋅Harris, J.⋅Jankovic, J.⋅Jankovic, J.⋅Hunter, C.⋅Hunter, C.⋅Lang, A.⋅Lang, A.⋅Kleimer-Fisman, G.⋅Kleimer-Fisman, G.⋅Nieves, A.⋅Nieves, A.⋅So, J.⋅So, J.⋅Factor, S.⋅Factor, S.⋅Evans, S.⋅Evans, S.⋅Manyam, B.⋅Manyam, B.⋅Wulbrecht, B.⋅Wulbrecht, B.⋅Walker, F.⋅Walker, F.⋅Hunt, V.⋅Hunt, V.⋅Gordon, M.F.⋅Gordon, M.F.⋅Hamman, J.⋅Hamman, J.⋅Kang, U.J.⋅Kang, U.J.⋅Young, J.⋅Young, J.⋅Blindauer, K.⋅Blindauer, K.⋅Petit, J.⋅Petit, J.⋅Rao, J.⋅Rao, J.⋅Cook, M.⋅Cook, M.⋅Stacy, M.⋅Stacy, M.⋅Williamson, K.⋅Williamson, K.⋅Pullman, R.S.⋅Pullman, R.S.⋅Boyar, K.⋅Boyar, K.⋅Leehey, M.⋅Leehey, M.⋅Derian, T.⋅Derian, T.⋅Gordon, P.⋅Gordon, P.⋅Werner, J. and Werner, J.Movement disorders : official journal of the Movement Disorder Society. , vol. 19, (no. 6), pp. 649-55, 2004/Jun.
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False positive rates in association studies as a function of degree of stratification.Koller, Daniel⋅Peacock, Munro⋅Lai, Dongbing⋅Foroud, Tatiana M and Econs, Michael JJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. , vol. 19, (no. 8), pp. 1291-5, 2004/Aug.
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Genetics of Parkinson diseasePankratz, Nathan and Foroud, TatianaNeurotherapeutics, vol. 1, (no. 2), pp. 242, 20040400.
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Genetics of Parkinson diseasePankratz, Nathan and Foroud, TatianaNeuroRx : the journal of the American Society for Experimental NeuroTherapeutics, vol. 1, (no. 2), pp. 242, 2004-Apr.
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