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Genetic counseling certificate program: A program evaluation of undergraduate exposure to genetic counseling.
Published in:
Journal of Genetic Counseling, 2022, v. 31, n. 4, p. 1003, doi. 10.1002/jgc4.1564
By:
- McGraw, Erin;
- Rispoli, Jessica;
- Horner, Michele B.;
- Heiman, Gary A.
Publication type:
Article
Evaluation of depression risk in LGI1 mutation carriers.
Published in:
Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1685, doi. 10.1111/j.1528-1167.2010.02677.x
By:
- Heiman, Gary A.;
- Kamberakis, Kay;
- Gill, Richard;
- Kalachikov, Sergey;
- Pedley, Timothy A.;
- Allen Hauser, W.;
- Ottman, Ruth
Publication type:
Article
Seizure remission and relapse in adults with intractable epilepsy: A cohort study.
Published in:
Epilepsia (Series 4), 2008, v. 49, n. 8, p. 1440, doi. 10.1111/j.1528-1167.2008.01601.x
By:
- Choi, Hyunmi;
- Heiman, Gary;
- Pandis, Dionysis;
- Cantero, Julio;
- Resor, Stanley R.;
- Gilliam, Frank G.;
- Hauser, W. Allen
Publication type:
Article
Polygenic and environmental determinants of tics in the Avon Longitudinal Study of Parents and Children.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2023, v. 192, n. 5/6, p. 73, doi. 10.1002/ajmg.b.32924
By:
- Abdulkadir, Mohamed;
- Tischfield, Jay A.;
- Heiman, Gary A.;
- Hoekstra, Pieter J.;
- Dietrich, Andrea
Publication type:
Article
The Tourette International Collaborative Genetics (TIC Genetics) study, finding the genes causing Tourette syndrome: objectives and methods.
Published in:
European Child & Adolescent Psychiatry, 2015, v. 24, n. 2, p. 141, doi. 10.1007/s00787-014-0543-x
By:
- Dietrich, Andrea;
- Fernandez, Thomas;
- King, Robert;
- State, Matthew;
- Tischfield, Jay;
- Hoekstra, Pieter;
- Heiman, Gary
Publication type:
Article
Control of Alzheimer's Amyloid Beta Toxicity by the High Molecular Weight Immunophilin FKBP52 and Copper Homeostasis in Drosophila.
Published in:
PLoS ONE, 2010, v. 5, n. 1, p. 1, doi. 10.1371/journal.pone.0008626
By:
- Sanokawa-Akakura, Reiko;
- Weihuan Cao;
- Allan, Kirsten;
- Patel, Khyati;
- Ganesh, Anupama;
- Heiman, Gary;
- Burke, Richard;
- Kemp, Francis W.;
- Bogden, John D.;
- Camakaris, James;
- Birge, Raymond B.;
- Konsolaki, Mary
Publication type:
Article
Exclusion of the DYT1 locus in a non-Jewish family with early-onset dystonia.
Published in:
Movement Disorders, 1994, v. 9, n. 6, p. 626, doi. 10.1002/mds.870090608
By:
- Bressman, Susan B.;
- Hunt, Ann L.;
- Heiman, Gary A.;
- Brin, Mitchell F.;
- Burke, Robert E.;
- Fahn, Stanley;
- Trugman, Joel M.;
- de Leon, Deborah;
- Kramer, Patricia L.;
- Wilhelmsen, Kirk C.;
- Nygaard, Torbjoern G.
Publication type:
Article
Rare missense neuronal cadherin gene (CDH2) variants in specific obsessive-compulsive disorder and Tourette disorder phenotypes.
Published in:
European Journal of Human Genetics, 2013, v. 21, n. 8, p. 850, doi. 10.1038/ejhg.2012.245
By:
- Moya, Pablo R;
- Dodman, Nicholas H;
- Timpano, Kiara R;
- Rubenstein, Liza M;
- Rana, Zaker;
- Fried, Ruby L;
- Reichardt, Louis F;
- Heiman, Gary A;
- Tischfield, Jay A;
- King, Robert A;
- Galdzicka, Marzena;
- Ginns, Edward I;
- Wendland, Jens R
Publication type:
Article
Evidence for Genetic Linkage Between a Polymorphism in the Adenosine 2A Receptor and Panic Disorder.
Published in:
Neuropsychopharmacology, 2004, v. 29, n. 3, p. 558, doi. 10.1038/sj.npp.1300311
By:
- Hamilton, Steven P.;
- Slager, Susan L.;
- de Leon, Ada Baisre;
- Heiman, Gary A.;
- Klein, Donald F.;
- Hodge, Susan E.;
- Weissman, Myrna M.;
- Fyer, Abby J.;
- Knowles, James A.
Publication type:
Article
Clinical and EEG factors associated with antiseizure medication resistance in idiopathic generalized epilepsy.
Published in:
Epilepsia (Series 4), 2022, v. 63, n. 1, p. 150, doi. 10.1111/epi.17104
By:
- Kamitaki, Brad K.;
- Janmohamed, Mubeen;
- Kandula, Padmaja;
- Elder, Christopher;
- Mani, Ram;
- Wong, Stephen;
- Perucca, Piero;
- O'Brien, Terence J.;
- Lin, Haiqun;
- Heiman, Gary A.;
- Choi, Hyunmi
Publication type:
Article
Mood disorders in familial epilepsy: A test of shared etiology.
Published in:
Epilepsia (Series 4), 2018, v. 59, n. 2, p. 431, doi. 10.1111/epi.13985
By:
- Insel, Beverly J.;
- Ottman, Ruth;
- Heiman, Gary A.
Publication type:
Article
In response: Drug-resistant epilepsy in adults: outcome trajectories after failure of two medications.
Published in:
Epilepsia (Series 4), 2016, v. 57, n. 9, p. 1526, doi. 10.1111/epi.13487
By:
- Choi, Hyunmi;
- Hayat, Matthew J.;
- Zhang, Ruiqi;
- Hirsch, Lawrence J.;
- Bazil, Carl;
- Mendiratta, Anil;
- Kato, Kenneth;
- Javed, Asif;
- Legge, Alexander W.;
- Buchsbaum, Richard;
- Resor, Stanley;
- Heiman, Gary
Publication type:
Article
Drug-resistant epilepsy in adults: Outcome trajectories after failure of two medications.
Published in:
Epilepsia (Series 4), 2016, v. 57, n. 7, p. 1152, doi. 10.1111/epi.13406
By:
- Choi, Hyunmi;
- Hayat, Matthew J.;
- Zhang, Ruiqi;
- Hirsch, Lawrence J.;
- Bazil, Carl W.;
- Mendiratta, Anil;
- Kato, Kenneth;
- Javed, Asif;
- Legge, Alexander W.;
- Buchsbaum, Richard;
- Resor, Stanley;
- Heiman, Gary A.
Publication type:
Article
Empiric Recurrence Risk Estimates for Chronic Tic Disorders: Implications for Genetic Counseling.
Published in:
Frontiers in Neurology, 2020, p. N.PAG, doi. 10.3389/fneur.2020.00770
By:
- Heiman, Gary A.;
- Rispoli, Jessica;
- Seymour, Christine;
- Leckman, James F.;
- King, Robert A.;
- Fernandez, Thomas V.
Publication type:
Article
Functional evaluations of Genes Disrupted in Patients with Tourette's Disorder.
Published in:
Frontiers in Psychiatry, 2016, p. 1, doi. 10.3389/fpsyt.2016.00011
By:
- Nawei Sun;
- Tischfield, Jay A.;
- King, Robert A.;
- Heiman, Gary A.;
- Tsetsos, Fotis;
- Georgitsi, Marianthi
Publication type:
Article
Rate of manifesting carriers and other unexpected findings on carrier screening.
Published in:
Prenatal Diagnosis, 2023, v. 43, n. 1, p. 117, doi. 10.1002/pd.6289
By:
- Clevenger, Sydney K.;
- Brandt, Justin S.;
- Khan, Shama P.;
- Shingala, Pranali;
- Carrick, Jillian;
- Aluwalia, Ruchi;
- Heiman, Gary A.;
- Ashkinadze, Elena
Publication type:
Article
Reproductive male partner testing when the female is identified to be a genetic disease carrier.
Published in:
Prenatal Diagnosis, 2021, v. 41, n. 1, p. 21, doi. 10.1002/pd.5824
By:
- Simone, Laurie;
- Khan, Shama;
- Ciarlariello, Molly;
- Lin, Julia;
- Trackman, Sarah;
- Heiman, Gary A.;
- Ashkinadze, Elena
Publication type:
Article
Relative risk for genetic associations: the case-parent triad as a variant of case-cohort design.
Published in:
2002
By:
- Ahsan, Habibul;
- Hodge, Susan E;
- Heiman, Gary A;
- Begg, Melissa D;
- Susser, Ezra S
Publication type:
journal article
Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31.
Published in:
1999
By:
- Nygaard, Torbjoern G.;
- Raymond, Deborah;
- Chen, Caiping;
- Nishino, Ichizo;
- Greene, Paul E.;
- Jennings, Danna;
- Heiman, Gary A.;
- Klein, Christine;
- Saunders-Pullman, Rachel J.;
- Kramer, Patricia;
- Ozelius, Laurie J.;
- Bressman, Susan B.;
- Nygaard, T G;
- Raymond, D;
- Chen, C;
- Nishino, I;
- Greene, P E;
- Jennings, D;
- Heiman, G A;
- Klein, C
Publication type:
journal article
Long-term treatment response and fluorodopa positron emission tomographic scanning of parkinsonism in a family with dopa-responsive dystonia.
Published in:
1992
By:
- Nygaard, Torbjoern G.;
- Takahashi, Hirohide;
- Heiman, Gary A.;
- Snow, Barry J.;
- Fahn, Stanley;
- Calne, Donald B.;
- Nygaard, T G;
- Takahashi, H;
- Heiman, G A;
- Snow, B J;
- Fahn, S;
- Calne, D B
Publication type:
journal article
Centralizing the non‐central chi‐square: a new method to correct for population stratification in genetic case‐control association studies.
Published in:
Genetic Epidemiology, 2006, v. 30, n. 4, p. 277, doi. 10.1002/gepi.20143
By:
- Prakash Gorroochurn;
- Gary A. Heiman;
- Susan E. Hodge;
- David A. Greenberg
Publication type:
Article
New simple tests for age-at-onset anticipation: Application to panic disorder.
Published in:
Genetic Epidemiology, 2005, v. 28, n. 3, p. 256, doi. 10.1002/gepi.20057
By:
- W.Y. Tsai;
- Gary A. Heiman;
- Susan E. Hodge
Publication type:
Article
GDNF gene is associated with tourette syndrome in a family study.
Published in:
Movement Disorders, 2015, v. 30, n. 8, p. 1115, doi. 10.1002/mds.26279
By:
- Huertas-Fernández, Ismael;
- Gómez-Garre, Pilar;
- Madruga-Garrido, Marcos;
- Bernal-Bernal, Inmaculada;
- Bonilla-Toribio, Marta;
- Martín-Rodríguez, Juan Francisco;
- Cáceres-Redondo, María Teresa;
- Vargas-González, Laura;
- Carrillo, Fátima;
- Pascual, Alberto;
- Tischfield, Jay A.;
- King, Robert A.;
- Heiman, Gary A.;
- Mir, Pablo
Publication type:
Article
Common and rare alleles of the serotonin transporter gene, SLC6A4, associated with Tourette's disorder.
Published in:
Movement Disorders, 2013, v. 28, n. 9, p. 1263, doi. 10.1002/mds.25460
By:
- Moya, Pablo R.;
- Wendland, Jens R.;
- Rubenstein, Liza M.;
- Timpano, Kiara R.;
- Heiman, Gary A.;
- Tischfield, Jay A.;
- King, Robert A.;
- Andrews, Anne M.;
- Ramamoorthy, Samanda;
- McMahon, Francis J.;
- Murphy, Dennis L.
Publication type:
Article
Mood and cognition in leucine-rich repeat kinase 2 G2019S Parkinson's disease.
Published in:
Movement Disorders, 2011, v. 26, n. 10, p. 1875, doi. 10.1002/mds.23746
By:
- Shanker, Vicki;
- Groves, Mark;
- Heiman, Gary;
- Palmese, Christina;
- Saunders-Pullman, Rachel;
- Ozelius, Laurie;
- Raymond, Deborah;
- Bressman, Susan
Publication type:
Article
Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with ε-sarcoglycan mutations.
Published in:
Movement Disorders, 2008, v. 23, n. 4, p. 588, doi. 10.1002/mds.21785
By:
- Raymond, Deborah;
- Saunders-Pullman, Rachel;
- de Carvalho Aguiar, Patricia;
- Schule, Birgitt;
- Kock, Norman;
- Friedman, Jennifer;
- Harris, Juliette;
- Ford, Blair;
- Frucht, Steven;
- Heiman, Gary A.;
- Jennings, Danna;
- Doheny, Dana;
- Brin, Mitchell F.;
- de Leon Brin, Deborah;
- Multhaupt-Buell, Trisha;
- Lang, Anthony E.;
- Kurlan, Roger;
- Klein, Christine;
- Ozelius, Laurie;
- Bressman, Susan
Publication type:
Article
An Analytic Solution to the Computation of Power and Sample Size for Genetic Association Studies under a Pleiotropic Mode of Inheritance.
Published in:
Human Heredity, 2017, v. 81, n. 4, p. 194, doi. 10.1159/000457135
By:
- Gordon, Derek;
- Londono, Douglas;
- Patel, Payal;
- Kim, Wonkuk;
- Finch, Stephen J.;
- Heiman, Gary A.
Publication type:
Article
An Improved Delta-Centralization Method for Population Stratification.
Published in:
Human Heredity, 2011, v. 71, n. 3, p. 180, doi. 10.1159/000327728
By:
- Gorroochurn, Prakash;
- Hodge, Susan E.;
- Heiman, Gary A.;
- Greenberg, David A.
Publication type:
Article
Comments on ‘Delta-Centralization Fails to Control for Population Stratification in Genetic Association Studies’.
Published in:
Human Heredity, 2010, v. 69, n. 4, p. 295, doi. 10.1159/000298766
By:
- Gorroochurn, Prakash;
- Hodge, Susan E.;
- Heiman, Gary A.;
- Greenberg, David A.
Publication type:
Article
Comments on: Review and Evaluation of Methods Correcting for Population Stratification with a Focus on Underlying Statistical Principles.
Published in:
Human Heredity, 2009, v. 67, n. 2, p. 145, doi. 10.1159/000179562
By:
- Gorroochurn, Prakash;
- Hodge, Susan E.;
- Heiman, Gary A.;
- Greenberg, David A.
Publication type:
Article
A Unified Approach for Quantifying, Testing and Correcting Population Stratification in Case-Control Association Studies.
Published in:
Human Heredity, 2007, v. 64, n. 3, p. 149, doi. 10.1159/000102988
By:
- Gorroochurn, Prakash;
- Hodge, Susan E.;
- Heiman, Gary A.;
- Greenberg, David A.
Publication type:
Article

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