Cognitive performance of GBA mutation carriers with early-onset PD: The CORE-PD study von ALCALAY, R. N, CACCAPPOLO, E, LOUIS, E, COMELLA, C, COLCHER, A, JENNINGS, D, NANCE, M, BRESSMAN, S, SCOTT, W. K, TANNER, C, MICKEL, S, ANDREWS, H, MEJIA-SANTANA, H, WATERS, C, FAHN, S, COTE, L, FRUCHT, S, FORD, B, REZAK, M, NOVAK, K, FRIEDMAN, J. H, PFEIFFER, R, MARSH, L, TANG, M.-X, HINER, B, SIDEROWF, A, PAYAMI, H, MOLHO, E, FACTOR, S, OTTMAN, R, CLARK, L. N, MARDER, K, ROSADO, L, ORBE REILLY, M, RUIZ, D, ROSS, B, VERBITSKY, M, KISSELEV, S

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Diagnostic exome sequencing in children: A survey of parental understanding, experience and psychological impact von Wynn, J., Ottman, R., Duong, J., Wilson, A.L., Ahimaz, P., Martinez, J., Rabin, R., Rosen, E., Webster, R., Au, C., Cho, M.T., Egan, C., Guzman, E., Primiano, M., Shaw, J.E., Sisson, R., Klitzman, R.L., Appelbaum, P.S., Lichter‐Konecki, U., Anyane‐Yeboa, K., Iglesias, A., Chung, W.K.

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Deep learning, 3D ultrastructural analysis reveals quantitative differences in platelet and organelle packing in COVID-19/SARSCoV2 patient-derived platelets von Matharu, Sagar S, Nordmann, Cassidy S, Ottman, Kurtis R, Akkem, Rahul, Palumbo, Douglas, Cruz, Denzel R D, Campbell, Kenneth, Sievert, Gail, Sturgill, Jamie, Porterfield, James Z, Joshi, Smita, Alfar, Hammodah R, Peng, Chi, Pokrovskaya, Irina D, Kamykowski, Jeffrey A, Wood, Jeremy P, Garvy, Beth, Aronova, Maria A, Whiteheart, Sidney W, Leapman, Richard D, Storrie, Brian

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Is there a one-way street from essential tremor to Parkinson's disease? Possible biological ramifications von Louis, E. D., Ottman, R.

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Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease von CLARK, L. N, ROSS, B. M, FORD, B, FRUCHT, S, OTTMAN, R, MARDER, K, WANG, Y, MEJIA-SANTANA, H, HARRIS, J, LOUIS, E. D, COTE, L. J, ANDREWS, H, FAHN, S, WATERS, C

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Frequency of LRRK2 mutations in early-and late-onset Parkinson disease von CLARK, L. N, WANG, Y, WATERS, C, FORD, B, FRUCHT, S, OTTMAN, R, MARDER, K, KARLINS, E, SAITO, L, MEJIA-SANTANA, H, HARRIS, J, LOUIS, E. D, COTE, L. J, ANDREWS, H, FAHN, S

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LGI1 mutations in autosomal dominant partial epilepsy with auditory features von OTTMAN, R, WINAWER, M. R, KALACHIKOV, S, BARKER-CUMMINGS, C, GILLIAM, T. C, PEDLEY, T. A, HAUSER, W. A

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Accuracy of family history information on epilepsy and other seizure disorders von OTTMAN, R, BARKER-CUMMINGS, C, LEIBSON, C. L, VASOLI, V. M, HAUSER, W. A, BUCHHALTER, J. R

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Premorbid weight, body mass, and varsity athletics in ALS von SCARMEAS, N, SHIH, T, STERN, Y, OTTMAN, R, ROWLAND, L. P

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Recent Developments in Molecular Epidemiology: A Study of the Effects of Environmental Polycyclic Aromatic Hydrocarbons on Birth Outcomes in Poland von Perera, Frederica P., Whyatt, Robin M., Jedrychowski, Wieslaw, Rauh, Virginia, Manchester, David, Santella, Regina M., Ottman, Ruth

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Olfaction in Parkin heterozygotes and compound heterozygotes: The CORE-PD study von ALCALAY, R. N, SIDEROWF, A, FAHN, S, COTE, L, FRUCHT, S, FORD, B, ORBE-REILLY, M, ROSS, B, VERBITSKY, M, KISSELEV, S, COMELLA, C, COLCHER, A, OTTMAN, R, JENNINGS, D, NANCE, M, BRESSMAN, S, SCOTT, W. K, TANNER, C, MICKEL, S, REZAK, M, NOVAK, K. E, FRIEDMAN, J. H, PFEIFFER, R, CACCAPPOLO, E, MARSH, L, HINER, B, CLARK, L. N, MARDER, K, MEJIA-SANTANA, H, TANG, M.-X, ROSADO, L, LOUIS, E, RUIZ, D, WATERS, C

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Increased risk for recurrent major depression in DYT1 dystonia mutation carriers von HEIMAN, G. A, OTTMAN, R, SAUNDERS-PULLMAN, R. J, OZELIUS, L. J, RISCH, N. J, BRESSMAN, S. B

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Smoking and parkinson's disease in twins von TANNER, C. M, GOLDMAN, S. M, ASTON, D. A, OTTMAN, R, ELLENBERG, J, MAYEUX, R, LANGSTON, J. W

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Identification of epilepsy genes in human and mouse von Meisler, M H, Kearney, J, Ottman, R, Escayg, A

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Subclinical tremor in normal controls with versus without a family history of essential tremor: data from the United States and Turkey von Louis, E. D., Dogu, O., Ottman, R.

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Synergistic effects of traumatic head injury and apolipoprotein-ε4 in patients with Alzheimer's disease von MAYEUX, R, OTTMAN, R, MAESTRE, G, NGAI, C, TANG, M.-X, GINSBERG, H, CHUN, M, TYCKO, B, SHELANSKI, M

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Analysis of Genetically Complex Epilepsies von Ottman, Ruth

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Familial clustering of seizure types within the idiopathic generalized epilepsies von Winawer, M R, Marini, C, Grinton, B E, Rabinowitz, D, Berkovic, S F, Scheffer, I E, Ottman, R

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The relation between depression and parkin genotype: The CORE-PD study von Srivastava, A, Tang, M.-X, Mejia-Santana, H, Rosado, L, Louis, E.D, Caccappolo, E, Comella, C, Colcher, A, Siderowf, 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, Alcalay, R.N, Ross, B, Orbe Reilly, M, Rezak, M, Novak, K, Friedman, J.H, Pfeiffer, R.D, Marsh, L, Hiner, B, Merle, D, Ottman, R, Clark, L.N, Marder, K

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What’s at stake? Genetic information from the perspective of people with epilepsy and their family members von Shostak, Sara, Zarhin, Dana, Ottman, Ruth

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