Catharine Freyer, MBA | The UCSF Division of Neurology at ZSFG

Division Administrator

M_Neurology

[email protected]

Publications

Return of individual results in epilepsy genomic research: A view from the field.

Epilepsia

Ottman R, Freyer C, Mefford HC, Poduri A, Lowenstein DH

Phenotypic analysis of 303 multiplex families with common epilepsies.

Brain : a journal of neurology

Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability.

Human genetics

Bramswig NC, Lüdecke HJ, Hamdan FF, Altmüller J, Beleggia F, Elcioglu NH, Freyer C, Gerkes EH, Demirkol YK, Knupp KG, Kuechler A, Li Y, Lowenstein DH, Michaud JL, Park K, Stegmann APA, Veenstra-Knol HE, Wieland T, Wollnik B, Engels H, Strom TM, Kleefstra T, Wieczorek D

Ultra-rare genetic variation in common epilepsies: a case-control sequencing study.

The Lancet. Neurology

Surpassing the Target: How a Recruitment Campaign Transformed the Participant Accrual Trajectory in the Epilepsy Phenome/Genome Project.

Clinical and translational science

McGovern K, Karn CF, Fox K

The epilepsy phenome/genome project.

Clinical trials (London, England)

Abou-Khalil B, Alldredge B, Bautista J, Berkovic S, Bluvstein J, Boro A, Cascino G, Consalvo D, Cristofaro S, Crumrine P, Devinsky O, Dlugos D, Epstein M, Fahlstrom R, Fiol M, Fountain N, Fox K, French J, Freyer Karn C, Friedman D, Geller E, Glauser T, Glynn S, Haas K, Haut S, Hayward J, Helmers S, Joshi S, Kanner A, Kirsch H, Knowlton R, Kossoff E, Kuperman R, Kuzniecky R, Lowenstein D, McGuire S, Motika P, Nesbitt G, Novotny E, Ottman R, Paolicchi J, Parent J, Park K, Poduri A, Risch N, Sadleir L, Scheffer I, Shellhaas R, Sherr E, Shih JJ, Shinnar S, Singh R, Sirven J, Smith M, Sullivan J, Thio LL, Venkat A, Vining E, von Allmen G, Weisenberg J, Widdess-Walsh P, Winawer M