27 Publications (Page 1 of 2)
2006
Genetic Medicine
Conneally, P. M
JAMA, vol. 295, (no. 15), pp. 1841-1842, Apr 19, 2006. | Journal Article
 
Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia.
Pankratz, N.⋅Pankratz, N.⋅Pankratz, Nathan⋅Byder, Lisa⋅Byder, L.⋅Byder, L.⋅Halter, Cheryl⋅Halter, C.⋅Halter, C.⋅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.⋅Nichols, W.C.⋅Nichols, William C⋅Nichols, W.C.⋅Lyons, K.⋅Lyons, K.⋅Marder, K.⋅Marder, K.⋅Marshall, F.⋅Marshall, F.⋅Oakes, D.⋅Oakes, D.⋅Rudolph, A.⋅Rudolph, A.⋅Shinaman, A.⋅Shinaman, A.⋅Siemers, E.⋅Siemers, E.⋅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.⋅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.⋅De Angelis, M.⋅De Angelis, 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.⋅Wieler, M.⋅Wieler, M.⋅Tuite, P.⋅Tuite, P.⋅Schacherer, R.⋅Schacherer, R.⋅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. and Boyar, K.
Movement disorders : official journal of the Movement Disorder Society, vol. 21, (no. 1), pp. 45-9, 2006/Jan. | Journal Article
2005
Contribution of the LRP5 Gene to Normal Variation in Peak BMD in Women
Koller, Daniel⋅Ichikawa, Shoji⋅Johnson, ML⋅Lai, D.⋅Xuei, Xiaoling⋅Edenberg, Howard J⋅Conneally, P. M⋅Hui, Siu L⋅Johnston, CC⋅Peacock, Munro⋅Foroud, Tatiana M and Econs, Michael
Journal of Bone and Mineral Research, vol. 20, (no. 1), pp. 75-80, 2005. | Journal Article
2004
Confirmation of Linkage to Chromosome 1q for Peak Vertebral Bone Mineral Density in Premenopausal White Women
Econs, Michael⋅Koller, Daniel⋅Hui, Siu L⋅Fishburn, T.⋅Conneally, P. M⋅Johnston, CC J⋅Peacock, Munro and Foroud, Tatiana M
American Journal of Human Genetics, vol. 74, (no. 2), pp. 223-228, 2004. | Journal Article
 
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. | Journal Article
 
Genes influencing Parkinson disease onset: replication of PARK3 and identification of novel loci.
Pankratz, Nathan⋅Uniacke, S K⋅Halter, C A⋅Rudolph, Alice⋅Shults, Clifford W⋅Conneally, P. M⋅Foroud, T and Nichols, W C
Neurology, vol. 62, (no. 9), pp. 1616-8, 2004/May/11. | Journal Article
2003
Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families
Pankratz, N.⋅Pankratz, N.⋅Pankratz, Nathan⋅Nichols, W.C.⋅Nichols, William C⋅Nichols, W.C.⋅Uniacke, Sean K⋅Uniacke, S.K.⋅Uniacke, S.K.⋅Halter, Cheryl⋅Halter, C.⋅Halter, C.⋅Murrell, Jill R⋅Murrell, J.⋅Murrell, J.⋅Rudolph, A.⋅Rudolph, A.⋅Rudolph, Alice⋅Shults, Clifford W⋅Shults, C.W.⋅Shults, C.W.⋅Conneally, P. M⋅Conneally, P.M.⋅Conneally, P.M.⋅Foroud, Tatiana M⋅Foroud, T.⋅Foroud, T.⋅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.⋅Wieler, M.⋅Wieler, M.⋅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.⋅Werner, J.⋅Racette, B.⋅Racette, B.⋅Good, L.⋅Good, L.⋅Simon, D.⋅Simon, D.⋅Scollins, L.⋅Scollins, L.⋅Schwieterman, D.⋅Schwieterman, D.⋅Dewey, R.⋅Dewey, R.⋅Meacham, M.⋅Meacham, M.⋅Sutton, J.⋅Sutton, J.⋅Hutchinson, B.⋅Hutchinson, B.⋅Jog, M.⋅Jog, M.⋅Horn, C.⋅Horn, C.⋅Sethi, K.⋅Sethi, K.⋅Carpenter, J.⋅Carpenter, J.⋅Atchison, P.⋅Atchison, P.⋅Rolli, S.⋅Rolli, S.⋅Sudarsky, L.⋅Sudarsky, L.⋅Corwin, C.⋅Corwin, C.⋅Velickovic, M.⋅Velickovic, M.⋅Phipps, S.⋅Phipps, S.⋅Simuni, T.⋅Simuni, T.⋅Kaczmarek, A.⋅Kaczmarek, A.⋅Hermanowicz, N.⋅Hermanowicz, N.⋅Niswonger, S.⋅Niswonger, S.⋅Feigin, A.⋅Feigin, A.⋅Shannon, B.⋅Shannon, B.⋅Calabrese, V.⋅Calabrese, V.⋅Roberge, P.⋅Roberge, P.⋅Homes, H.⋅Homes, H.⋅Shulman, L.⋅Shulman, L.⋅Dustin, K.⋅Dustin, K.⋅Ajax, T.⋅Ajax, T.⋅Mannetter, J.⋅Mannetter, J.⋅Podskalny, G.D.⋅Podskalny, G.D.⋅Giffin, L.⋅Giffin, L.⋅Uitti, R.⋅Uitti, R.⋅Turk, M.F. and Turk, M.F.
Human Molecular Genetics, vol. 12, (no. 20), pp. 2599-608, Oct 16, 2003. | Journal Article
 
Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease.
Foroud, Tatiana⋅Foroud, Tatiana M⋅Uniacke, S K⋅Uniacke, SK⋅Liu, L⋅Liu, L⋅Pankratz, Nathan⋅Pankratz, N⋅Rudolph, Alice⋅Rudolph, A⋅Halter, C⋅Halter, C⋅Shults, C⋅Shults, C⋅Marder, K⋅Marder, K⋅Conneally, PM⋅Conneally, P. M⋅Nichols, WC⋅Nichols, W C and others
Neurology, vol. 60, (no. 5), pp. 796-801, 2003/Mar/11. | Journal Article
 
Linkage of structure at the proximal femur to chromosomes 3, 7, 8, and 19.
Koller, Daniel⋅White, Kenneth E⋅Liu, G⋅Hui, Siu L⋅Conneally, P. M⋅Johnston, C C⋅Econs, Michael J⋅Foroud, Tatiana M and Peacock, Munro
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, vol. 18, (no. 6), pp. 1057-65, 2003/Jun. | Journal Article
 
The complexity of complex diseases.
Conneally, P. M
American journal of human genetics. , vol. 72, (no. 2), pp. 229-32, 2003/Feb. | Journal Article
2002
Evaluation of psychological symptoms among presymptomatic HD gene carriers as measured by selected MMPI scales.
Close Kirkwood, Sandra⋅Close Kirkwood, Sandra⋅Siemers, Eric⋅Siemers, Eric⋅Viken, Richard J⋅Viken, Richard J⋅Hodes, M E⋅Hodes, M.E⋅Conneally, P.Michael⋅Conneally, P. M⋅Christian, Joe C⋅Christian, Joe C⋅Foroud, Tatiana and Foroud, Tatiana
Journal of psychiatric research, vol. 36, (no. 6), pp. 377-82, 2002 Nov-Dec. | Journal Article
 
Linkage disequilibrium between the beta frequency of the human EEG and a GABAA receptor gene locus.
Porjesz, Bernice⋅Almasy, Laura⋅Edenberg, Howard J⋅Wang, Kongming⋅Chorlian, David B⋅Foroud, Tatiana M⋅Goate, Alison⋅Rice, John P⋅O'connor, Sean J⋅Rohrbaugh, John W⋅Kuperman, Samuel⋅Bauer, Lance O⋅Crowe, Raymond R⋅Schuckit, Marc A⋅Hesselbrock, Victor M⋅Conneally, P. M⋅Tischfield, Jay A⋅Li, Ting Kai⋅Reich, Theodore and Begleiter, Henri
Proceedings of the National Academy of Sciences of the United States of America, vol. 99, (no. 6), pp. 3729-33, 2002/Mar/19. | Journal Article
 
Linkage stratification and mutation analysis at the Parkin locus identifies mutation positive Parkinson's disease families.
Nichols, William C⋅Pankratz, Nathan⋅Uniacke, S K⋅Pauciulo, M W⋅Halter, C⋅Rudolph, Alice⋅Conneally, P. M and Foroud, Tatiana M
Journal of medical genetics, vol. 39, (no. 7), pp. 489-92, 2002/Jul. | Journal Article
 
Longitudinal Personality Changes Among Presymptomatic Huntington Disease Gene Carriers
Kirkwood, SC⋅Siemers, E.⋅Viken, Richard J⋅Modes, ME⋅Conneally, P. M⋅Christian, Joe C and Foroud, Tatiana M
Cognitive and Behavioral Neurology, vol. 15, (no. 3), pp. 192-197, 2002. | Journal Article
 
Sibling pair linkage and association studies between peak bone mineral density and the gene locus for the osteoclast-specific subunit (OC116) of the vacuolar proton pump on chromosome 11p12-13.
Carn, Gwenaelle⋅Koller, Daniel⋅Peacock, Munro⋅Hui, Siu L⋅Evans, Wayne E⋅Conneally, P. M⋅Johnston, C C⋅Foroud, Tatiana M and Econs, Michael J
The Journal of clinical endocrinology and metabolism, vol. 87, (no. 8), pp. 3819-24, 2002/Aug. | Journal Article
2001
Genome Screen for Quantitative Trait Loci Underlying Normal Variation in Femoral Structure
Koller, Daniel⋅Liu, Guangda⋅Econs, Michael⋅Hui, Siu L⋅Morin, Phillip A⋅Joslyn, G.⋅Rodriguez, LA⋅Conneally, P. M⋅Christian, Joe C⋅Johnston, CC J⋅Foroud, Tatiana M and Peacock, Munro
Journal of Bone and Mineral Research, vol. 16, (no. 6), pp. 985-991, 2001. | Journal Article
2000
Confirmation of subtle motor changes among presymptomatic carriers of the Huntington disease gene.
Kirkwood, S C⋅Siemers, E⋅Bond, C⋅Conneally, P. M⋅Christian, Joe C and Foroud, Tatiana M
Archives of neurology, vol. 57, (no. 7), pp. 1040-4, 2000/Jul. | Journal Article
 
Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis.
Koller, Daniel⋅Econs, Michael J⋅Morin, Phillip A⋅Christian, Joe C⋅Hui, Siu L⋅Parry, P⋅Curran, M E⋅Rodriguez, L A⋅Conneally, P. M⋅Joslyn, G⋅Peacock, Munro⋅Johnston, C C and Foroud, Tatiana M
The Journal of clinical endocrinology and metabolism, vol. 85, (no. 9), pp. 3116-20, 2000/Sep. | Journal Article
1999
Description of the Genetic Analysis Workshop 11 Collaborative Study on the Genetics of Alcoholism.
Begleiter, Henri⋅Reich, Theodore⋅Nurnberger, John I⋅Nurnberger Jr., J.⋅Li, T K⋅Conneally, P. M⋅Edenberg, Howard J⋅Crowe, R⋅Kuperman, Samuel⋅Schuckit, Marc A⋅Bloom, Floyd E⋅Hesselbrock, Victor M⋅Porjesz, B⋅Cloninger, C R⋅Rice, J and Goate, A
Genetic epidemiology, vol. 17 Suppl 1, pp. S25-30, 1999. | Journal Article
 
Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers.
Kirkwood, S.C.⋅Kirkwood, S C⋅Siemers, E.⋅Siemers, E⋅Stout, J.C.⋅Stout, Julie C⋅Hodes, M.E.⋅Hodes, M E⋅Conneally, P.M.⋅Conneally, P. M⋅Christian, Joe C⋅Christian, J.C.⋅Foroud, T. and Foroud, Tatiana M
Archives of Neurology, vol. 56, (no. 5), pp. 563-8, 1999/May. | Journal Article
 
Sibling Pair Linkage and Association Studies between Bone Mineral Density and the Insulin-Like Growth Factor I Gene Locus
Takacs, I.⋅Koller, Daniel⋅Peacock, Munro⋅Christian, Joe C⋅Hui, Siu L⋅Conneally, P. M⋅Johnston, CC J⋅Foroud, Tatiana M and Econs, Michael
Journal of Clinical Endocrinology and Metabolism, vol. 84, (no. 12), pp. 4467-4471, 1999. | Journal Article
1998
Linkage of a QTL contributing to normal variation in bone mineral density to chromosome 11q12-13.
Koller, Daniel⋅Rodriguez, L A⋅Christian, Joe C⋅Slemenda, Charles W⋅Econs, Michael J⋅Hui, Siu L⋅Morin, Phillip A⋅Conneally, P. M⋅Joslyn, G⋅Curran, M E⋅Peacock, Munro⋅Johnston, C C and Foroud, Tatiana M
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, vol. 13, (no. 12), pp. 1903-8, 1998/Dec. | Journal Article
 
Quantitative trait loci analysis of human event-related brain potentials: P3 voltage.
Begleiter, Henri⋅Porjesz, B⋅Reich, Theodore⋅Edenberg, Howard J⋅Goate, Alison⋅Blangero, J⋅Almasy, L⋅Foroud, Tatiana M⋅Van Eerdewegh, P⋅Polich, John⋅Rohrbaugh, John W⋅Kuperman, Samuel⋅Bauer, Lance O⋅O’Connor, S.J.⋅O'connor, Sean J⋅Chorlian, D B⋅Li, T K⋅Conneally, P. M⋅Hesselbrock, Victor M⋅Rice, John P⋅Schuckit, Marc A⋅Cloninger, R⋅Nurnberger Jr., J.⋅Nurnberger, John I⋅Crowe, R and Bloom, Floyd E
Electroencephalography and Clinical Neurophysiology, vol. 108, (no. 3), pp. 244-50, 1998/Apr. | Journal Article
1997
Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32.
Nichols, William C⋅Koller, Daniel⋅Slovis, Bonnie S⋅Foroud, Tatiana M⋅Terry, V H⋅Arnold, N D⋅Siemieniak, D R⋅Wheeler, L⋅Phillips, John A⋅Newman, John H⋅Conneally, P. M⋅Ginsburg, David and Loyd, James E
Nature genetics, vol. 15, (no. 3), pp. 277-80, 1997/Mar. | Journal Article
 
The presence of genetic anticipation suggests that the molecular basis of familial primary pulmonary hypertension may be trinucleotide repeat expansion.
Loyd, James E⋅Slovis, Bonnie S⋅Phillips, John A⋅Butler, Merlin G⋅Foroud, Tatiana M⋅Conneally, P. M and Newman, John H
Chest, vol. 111, (no. 6 Suppl), pp. 82S-83S, 1997/Jun. | Journal Article