Prenatal Toxicology Screening for Substance Abuse in Research: Codes and Consequences

av Rohan, AJ, Monk, C, Marder, K, Reame, N
Publicerad 2011

Dietary intake in adults at risk for Huntington disease: Analysis of PHAROS Research Participants

av Marder, K, Zhao, H, Eberly, S, Tanner, C M., Oakes, D, Shoulson, I
Publicerad 2009

Developmental malformations in Huntington disease: neuropathologic evidence of focal neuronal migration defects in a subset of adult brains

av Hickman, R. A., Faust, P. L., Rosenblum, M. K., Marder, K., Mehler, M. F., Vonsattel, J. P.
I publikationen Acta Neuropathol (2021)

Alzheimer's disease after remote head injury: an incidence study.

av Schofield, P W, Tang, M, Marder, K, Bell, K, Dooneief, G, Chun, M, Sano, M, Stern, Y, Mayeux, R
Publicerad 1997

Association between the APOE genotype and psychopathologic symptoms in Alzheimer's disease

av Scarmeas, N., Brandt, J., Albert, M., Devanand, D.P., Marder, K., Bell, K., Ciappa, A., Tycko, B., Stern, Y.
Publicerad 2002

Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations

av Pankratz, N, Kissell, D K., Pauciulo, M W., Halter, C A., Rudolph, A, Pfeiffer, R F., Marder, K S., Foroud, T, Nichols, W C.
Publicerad 2009

Incidence of and risk factors for cognitive impairment in an early Parkinson disease clinical trial cohort

av Uc, E Y., McDermott, M P., Marder, K S., Anderson, S W., Litvan, I, Como, P G., Auinger, P, Chou, K L., Growdon, J C.
Publicerad 2009

Is There a Genetic Susceptibility Locus for Parkinson’s Disease on Chromosome 22q13?

av Wilhelmsen, K., Mirel, D., Marder, K., Bernstein, M., Naini, A., Leal, S. M., Cote, L. J., Tang, M.-X., Freyer, G., Graziano, J., Mayeux, R.
I publikationen Ann Neurol (1997)

Motor signs during the course of Alzheimer disease

av Scarmeas, N., Hadjigeorgiou, G.M., Papadimitriou, A., Dubois, B., Sarazin, M., Brandt, J., Albert, M., Marder, K., Bell, K., Honig, L.S., Wegesin, D., Stern, Y.
Publicerad 2004

Motor signs predict poor outcomes in Alzheimer disease

av Scarmeas, N., Albert, M., Brandt, J., Blacker, D., Hadjigeorgiou, G., Papadimitriou, A., Dubois, B., Sarazin, M., Wegesin, D., Marder, K., Bell, K., Honig, L., Stern, Y.
Publicerad 2005

Transcranial sonography and functional imaging in glucocerebrosidase mutation Parkinson disease

av Barrett, MJ, Hagenah, J, Dhawan, V, Peng, S, Stanley, K, Raymond, D, Deik, A, Gross, SJ, Schreiber-Agus, N, Mirelman, A, Marder, K, Ozelius, LJ, Eidelberg, D, Bressman, SB, Saunders-Pullman, R
Publicerad 2012

Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease

av Clark, L.N., Ross, B.M., Wang, Y., Mejia-Santana, H., Harris, J., Louis, E.D., Cote, L.J., Andrews, H., Fahn, S., Waters, C., Ford, B., Frucht, S., Ottman, R., Marder, K.
Publicerad 2007

Mild cognitive impairment in Parkinson disease: A multicenter pooled analysis

av Aarsland, D., Bronnick, K., Williams-Gray, C., Weintraub, D., Marder, K., Kulisevsky, J., Burn, D., Barone, P., Pagonabarraga, J., Allcock, L., Santangelo, G., Foltynie, T., Janvin, C., Larsen, J.P., Barker, R.A., Emre, M.
Publicerad 2010

Alpha galactosidase A activity in Parkinson’s disease

av Alcalay, RN, Wolf, P, Levy, OA, Kang, UJ, Waters, C, Fahn, S, Ford, B, Kuo, SH, Vanegas, N, Shah, H, Liong, C, Narayan, S, Pauciulo, MW, Nichols, WC, Gan-Or, Z, Rouleau, GA, Chung, WK, Oliva, P, Keutzer, J, Marder, K, Zhang, XK
I publikationen Neurobiol Dis (2018)

Association of DRD2 and DRD3 Polymorphisms with Parkinson’s Disease in a Multiethnic Consortium

av McGuire, V., Van Den Eeden, S.K., Tanner, C.M., Kamel, F., Umbach, D M., Marder, K., Mayeux, R., Ritz, B., Ross, G. W., Petrovitch, H., Topol, B., Popat, R. A., Costello, S., Manthripragada, A. D., Southwick, A., Myers, R.M., Nelson, L. M.
Publicerad 2011

Coffee, ADORA2A, and CYP1A2: the caffeine connection in Parkinson’s disease

av Popat, R.A., Van Den Eeden, S.K., Tanner, C.M., Kamel, F., Umbach, D. M., Marder, K., Mayeux, R., Ritz, B., Ross, G. Webster, Petrovitch, H., Topol, B., McGuire, V., Costello, Sadie, Manthripragada, Angelika.D., Southwick, A., Myers, R.M., Nelson, L. M.
Publicerad 2011

Updated research nosology for HIV-associated neurocognitive disorders

av Antinori, A., Arendt, G., Becker, J.T., Brew, B.J., Byrd, D.A., Cherner, M., Clifford, D.B., Cinque, P., Epstein, L.G., Goodkin, K., Gisslen, M., Grant, I., Heaton, R.K., Joseph, J., Marder, K., Marra, C.M., McArthur, J.C., Nunn, M., Price, R.W., Pulliam, L., Robertson, K.R., Sacktor, N., Valcour, V., Wojna, V.E.
I publikationen Neurology (2007)

Motor phenotype of LRRK2 G2019S carriers in Early Onset Parkinson Disease

av Alcalay, RN, Mejia-Santana, H, Tang, M-X, Rosado, L, Verbitsky, M, Kisselev, S, Ross, B, Louis, ED, Comella, C, Colcher, A, Jennings, D, Nance, M, Bressman, S, Scott, WK, Tanner, C, Mickel, S, Andrews, H, Waters, C, Fahn, S, Cote, L, Frucht, S, Ford, B, Rezak, M, Novak, K, Friedman, JH, Pfeiffer, R, Marsh, L, Hiner, B, Siderowf, A, Caccappolo, E, Ottman, R, Clark, LN, Marder, K
Publicerad 2009

Frequency of known mutations in early onset PD; implication for genetic counseling: the CORE-PD study

av Alcalay, RN, Caccappolo, E, Mejia-Santana, H, Tang, M-X, Rosado, L, Ross, B, Verbitsky, M, Kisselev, S, Louis, ED, Comella, C, Colcher, A, Jennings, D, Nance, M, Bressman, S, Scott, WK, Tanner, C, Mickel, S, Andrews, H, Waters, C, Fahn, S, Cote, L, Frucht, S, Ford, B, Rezak, M, Novak, K, Friedman, JH, Pfeiffer, R, Marsh, L, Hiner, B, Siderowf, A, Ottman, R, Marder, K, Clark, LN
Publicerad 2010

The relation between depression and parkin genotype:the CORE-PD Study

av Srivastava, A, Tang, M-X, Mejia-Santana, H, Rosado, L, Louis, ED, Caccappolo, E, Comella, C, Colcher, A, Siderowf, A, Jennings, D, Nance, M, Bressman, S, Scott, WK, Tanner, C, Mickel, S, Andrews, H, Waters, C, Fahn, S, Cote, L, Frucht, S, Ford, B, Alcalay, RN, Ross, B, Rezak, M, Novak, K, Friedman, JH, Pfeiffer, R, Marsh, L, Hiner, B, Merle, D, Ottman, R, Clark, LN, Marder, K
Publicerad 2011