Gene-environment interaction and public health.

Por Ottman, R
Publicado em 1995

Higher risk of seizures in offspring of mothers than of fathers with epilepsy.

Por Ottman, R, Annegers, J F, Hauser, W A, Kurland, L T
Publicado em 1988

Segregation analysis of cryptogenic epilepsy and an empirical test of the validity of the results.

Por Ottman, R, Hauser, W A, Barker-Cummings, C, Lee, J H, Risch, N
Publicado em 1997

Genetic influences on myoclonic and absence seizures

Por Winawer, M.R., Rabinowitz, D., Pedley, T.A., Hauser, W.A., Ottman, R.
Publicado em 2003

Classification of partial seizure symptoms in genetic studies of the epilepsies

Por Choi, H., Winawer, M.R., Kalachikov, S., Pedley, T.A., Hauser, W.A., Ottman, R.
Publicado em 2006

Accuracy of family history information on epilepsy and other seizure disorders

Por Ottman, R., Barker-Cummings, C., Leibson, C.L., Vasoli, V.M., Hauser, W.A., Buchhalter, J.R.
Publicado em 2011

LGI1 mutations in autosomal dominant partial epilepsy with auditory features

Por Ottman, R., Winawer, M.R., Kalachikov, S., Barker-Cummings, C., Gilliam, T.C., Pedley, T.A., Hauser, W.A.
Publicado em 2004

Reliability of seizure classification using a semistructured interview

Por Ottman, R., Lee, J.H., Hauser, W.A., Hong, S., Hesdorffer, D., Schupf, N., Pedley, T.A., Scheuer, M.L.
Publicado em 1993

Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+

Por Poduri, A, Wang, Y, Gordon, D, Barral-Rodriguez, S, Barker-Cummings, C, Ulgen, A, Chitsazzadeh, V, Hill, R S., Risch, N, Hauser, W A., Pedley, T A., Walsh, C A., Ottman, R
Publicado em 2009

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

Por 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.
Publicado em 2007

Relationship between ambient air pollution and DNA damage in Polish mothers and newborns.

Por Whyatt, R M, Santella, R M, Jedrychowski, W, Garte, S J, Bell, D A, Ottman, R, Gladek-Yarborough, A, Cosma, G, Young, T L, Cooper, T B, Randall, M C, Manchester, D K, Perera, F P
Publicado em 1998

Altered language processing in autosomal dominant partial epilepsy with auditory features

Por Ottman, R, Rosenberger, L, Bagic, A, Kamberakis, K, Ritzl, E K., Wohlschlager, A M., Shamim, S, Sato, S, Liew, C, Gaillard, W D., Wiggs, E, Berl, M M., Reeves-Tyer, P, Baker, E H., Butman, J A., Theodore, W H.
Publicado em 2008

Motor phenotype of LRRK2 G2019S carriers in Early Onset Parkinson Disease

Por 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
Publicado em 2009

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

Por 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
Publicado em 2010

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

Por 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
Publicado em 2011

Predictors of Parkin Mutations in Early Onset Parkinson disease: the CORE-PD Study

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

Olfaction in Parkin heterozygotes and compound heterozygotes: The CORE-PD study

Por Alcalay, R.N., Siderowf, A., Ottman, R., Caccappolo, E., Mejia-Santana, H., Tang, M.-X., Rosado, L., Louis, E., Ruiz, D., Waters, C., Fahn, S., Cote, L., Frucht, S., Ford, B., Orbe-Reilly, M., Ross, B., Verbitsky, M., Kisselev, S., Comella, C., Colcher, A., Jennings, D., Nance, M., Bressman, S., Scott, W.K., Tanner, C., Mickel, S., Rezak, M., Novak, K.E., Friedman, J.H., Pfeiffer, R., Marsh, L., Hiner, B., Clark, L.N., Marder, K.
Publicado em 2011

Cognitive and motor function in long duration PARKIN PD

Por Alcalay, RN, Caccappolo, E, Mejia-Santana, H, Tang, M–X, Rosado, L, Orbe Reilly, M, Ruiz, D, Louis, ED, Comella, C, Nance, M, Bressman, S, Scott, WK, Tanner, C, Mickel, S, Waters, C, Fahn, S, Cote, L, Frucht, S, Ford, B, Rezak, M, Novak, K, Friedman, JH, Pfeiffer, R, Marsh, L, Hiner, B, Payami, H, Molho, E, Factor, SA, Nutt, J, Serrano, C, Arroyo, M, Ottman, R, Pauciulo, M, Nichols, W, Clark, LN, Marder, K
Publicado em 2014

Cognitive performance of GBA mutation carriers with early-onset PD: The CORE-PD study

Por Alcalay, R.N., Caccappolo, E., Mejia-Santana, H., Tang, M.-X., Rosado, L., Orbe Reilly, M., Ruiz, D., Ross, B., Verbitsky, M., Kisselev, S., Louis, E., Comella, C., Colcher, A., Jennings, D., Nance, M., Bressman, S., Scott, W.K., Tanner, C., Mickel, S., Andrews, H., Waters, C., Fahn, S., Cote, L., Frucht, S., Ford, B., Rezak, M., Novak, K., Friedman, J.H., Pfeiffer, R., Marsh, L., Hiner, B., Siderowf, A., Payami, H., Molho, E., Factor, S., Ottman, R., Clark, L.N., Marder, K.
Publicado em 2012