نتائج البحث - "Budman, C. L."

1

دورية أكاديمية

Genome-wide association study of Tourette's syndrome

المؤلفون: Scharf, J. M., Yu, D., Mathews, C. A., Neale, B. M., Stewart, S. E., Fagerness, J. A., Evans, P., Gamazon, E., Edlund, C. K., Service, S. K., Tikhomirov, A., Osiecki, L., Illmann, C., Pluzhnikov, A., Konkashbaev, A., Davis, L. K., Han, B., Crane, J., Moorjani, P., Crenshaw, A. T., Parkin, M. A., Reus, V. I., Lowe, T. L., Rangel-Lugo, M., Chouinard, S., Dion, Y., Girard, S., Cath, D. C., Smit, J. H., King, R. A., Fernandez, T. V., Leckman, J. F., Kidd, K. K., Kidd, J. R., Pakstis, A. J., State, M. W., Herrera, L. D., Romero, R., Fournier, E., Sandor, P., Barr, C. L., Phan, N., Gross-Tsur, V., Benarroch, F., Pollak, Y., Budman, C. L., Bruun, R. D., Erenberg, G., Naarden, A. L., Lee, P. C., Weiss, N., Kremeyer, B., Berrio, G. B., Campbell, D. D., Cardona Silgado, J. C., Ochoa, W. C., Mesa Restrepo, S. C., Muller, H., Valencia Duarte, A. V., Lyon, G. J., Leppert, M., Morgan, J., Weiss, R., Grados, M. A., Anderson, K., Davarya, S., Singer, H., Walkup, J., Jankovic, J., Tischfield, J. A., Heiman, G. A., Gilbert, D. L., Hoekstra, P. J., Robertson, M. M., Kurlan, R., Liu, C., Gibbs, J. R., Singleton, A., Hardy, J., Strengman, E., Ophoff, R. A., Wagner, M., Moessner, R., Mirel, D. B., Posthuma, D., Sabatti, C., Eskin, E., Conti, D. V., Knowles, J. A., Ruiz-Linares, A., Rouleau, G. A., Purcell, S., Heutink, P., Oostra, B. A., McMahon, W. M., Freimer, N. B., Cox, N. J., Pauls, D. L.

المساهمون: Han, B.

مصطلحات موضوعية: COPY NUMBER VARIANTS, COMMON VARIANTS, SLITRK1 VAR321, SCHIZOPHRENIA, FAMILY, INDIVIDUALS, DEPENDENCE, MUTATIONS, DISORDER, POLR3B, genetics, GWAS, neurodevelopmental disorder, tics, Tourette&apos, s syndrome

العلاقة: Molecular Psychiatry, Vol.18, pp.721-728; https://hdl.handle.net/10371/191623Test; 000319451600015; 2-s2.0-84878227013; 181250

الإتاحة: https://doi.org/10.1038/mp.2012.69Test
https://hdl.handle.net/10371/191623Test

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2

دورية أكاديمية

Genetic and phenotypic overlap of specific obsessive-compulsive and attention-deficit/hyperactive subtypes with Tourette syndrome

المؤلفون: Hirschtritt, M. E., Darrow, S. M., Illmann, C., Osiecki, L., Grados, M., Sandor, P., Dion, Y., King, R. A., Pauls, D., Budman, C. L., Cath, D. C., Greenberg, E., Lyon, G. J., Yu, D., McGrath, L. M., McMahon, W. M., Lee, P. C., Delucchi, K. L., Scharf, J. M., Mathews, C. A.

المصدر: Hirschtritt , M E , Darrow , S M , Illmann , C , Osiecki , L , Grados , M , Sandor , P , Dion , Y , King , R A , Pauls , D , Budman , C L , Cath , D C , Greenberg , E , Lyon , G J , Yu , D , McGrath , L M , McMahon , W M , Lee , P C , Delucchi , K L , Scharf , J M & Mathews , C A 2018 , ' Genetic and phenotypic overlap of ....

مصطلحات موضوعية: Attention-deficit/hyperactivity disorder, factors, heritability, latent classes, obsessive-compulsive disorder, Tourette syndrome, PSYCHIATRIC-DISORDERS, SYMPTOMS, ADHD, MODEL, TICS, COMPONENTS, CIRCUITS, NUMBER, COHORT, AGE

وصف الملف: application/pdf

العلاقة: https://research.rug.nl/en/publications/83fee7f6-6cc0-4c03-a4aa-f8bc5c3308bbTest

الإتاحة: https://doi.org/10.1017/S0033291717001672Test
https://hdl.handle.net/11370/83fee7f6-6cc0-4c03-a4aa-f8bc5c3308bbTest
https://research.rug.nl/en/publications/83fee7f6-6cc0-4c03-a4aa-f8bc5c3308bbTest
https://pure.rug.nl/ws/files/52684273/genetic_and_phenotypic_overlap_of_specific_obsessivecompulsive_and_attentiondeficithyperactive_subtypes_with_tourette_syndrome.pdfTest

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3

دورية أكاديمية

Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture

المؤلفون: Davis, L. K., Yu, D., Keenan, C. L., Gamazon, E. R., Konkashbaev, A. I., Derks, E. M., Neale, B. M., Yang, J., Lee, S. H., Evans, P., Barr, C. L., Bellodi, L., Benarroch, F., Berrio, G. B., Bienvenu, O. J., Bloch, M. H., Blom, R. M., Bruun, R. D., Budman, C. L., Camarena, B., Campbell, D., Cappi, C., Cardona Silgado, J. C., Cath, D. C., Cavallini, M. C., Chavira, D. A., Chouinard, S., Conti, D. V., Cook, E. H., Coric, V., Cullen, B. A., Deforce, D., Delorme, R., Dion, Y., Edlund, C. K., Egberts, K., Falkai, P., Fernandez, T. V., Gallagher, P. J., Garrido, H., Geller, D., Girard, Simon, Grabe, H. J., Grados, M. A., Greenberg, B. D., Gross-Tsur, V., Haddad, S., Heiman, G. A., Hemmings, S. M.J., Hounie, A. G., Illmann, C., Jankovic, J., Jenike, M. A., Kennedy, J. L., King, R. A., Kremeyer, B., Kurlan, R., Lanzagorta, N., Leboyer, M., Leckman, J. F., Lennertz, L., Liu, C., Lochner, C., Lowe, T. L., Macciardi, F., McCracken, J. T., McGrath, L. M., Mesa Restrepo, S. C., Moessner, R., Morgan, J., Muller, H., Murphy, D. L., Naarden, A. L., Ochoa, W. C., Ophoff, R. A., Osiecki, L., Pakstis, A. J., Pato, M. T., Pato, C. N., Piacentini, J., Pittenger, C., Pollak, Y., Rauch, S. L., Renner, T. J., Reus, V. I., Richter, M. A., Riddle, M. A., Robertson, M. M., Romero, R., Rosario, M. C., Rosenberg, D., Rouleau, G. A., Ruhrmann, S., Ruiz-Linares, A., Sampaio, A. S., Samuels, J., Sandor, P., Sheppard, B., Singer, H. S., Smit, J. H., Stein, D. J., Strengman, E., Tischfield, J. A., Valencia Duarte, A. V., Vallada, H., Van Nieuwerburgh, F., Veenstra-Vanderweele, J., Walitza, S., Wang, Y., Wendland, J. R., Westenberg, H. G.M., Shugart, Y. Y., Miguel, E. C., McMahon, W., Wagner, M., Nicolini, H., Posthuma, D., Hanna, G. L., Heutink, P., Denys, D., Arnold, P. D., Oostra, B. A., Nestadt, G., Freimer, N. B., Pauls, D. L., Wray, N. R., Stewart, S. E., Mathews, C. A., Knowles, J. A., Cox, N. J., Scharf, J. M.

مصطلحات موضوعية: Génétique

وصف الملف: application/pdf

العلاقة: https://constellation.uqac.ca/5144Test/; http://dx.doi.org/doi:10.1371/journal.pgen.1003864Test; https://constellation.uqac.ca/5144/1/Davis2013_Partitioning_the_heritability.pdfTest; Davis L. K., Yu D., Keenan C. L., Gamazon E. R., Konkashbaev A. I., Derks E. M., Neale B. M., Yang J., Lee S. H., Evans P., Barr C. L., Bellodi L., Benarroch F., Berrio G. B., Bienvenu O. J., Bloch M. H., Blom R. M., Bruun R. D., Budman C. L., Camarena B., Campbell D., Cappi C., Cardona Silgado J. C., Cath D. C., Cavallini M. C., Chavira D. A., Chouinard S., Conti D. V., Cook E. H., Coric V., Cullen B. A., Deforce D., Delorme R., Dion Y., Edlund C. K., Egberts K., Falkai P., Fernandez T. V., Gallagher P. J., Garrido H., Geller D., Girard Simon, Grabe H. J., Grados M. A., Greenberg B. D., Gross-Tsur V., Haddad S., Heiman G. A., Hemmings S. M.J., Hounie A. G., Illmann C., Jankovic J., Jenike M. A., Kennedy J. L., King R. A., Kremeyer B., Kurlan R., Lanzagorta N., Leboyer M., Leckman J. F., Lennertz L., Liu C., Lochner C., Lowe T. L., Macciardi F., McCracken J. T., McGrath L. M., Mesa Restrepo S. C., Moessner R., Morgan J., Muller H., Murphy D. L., Naarden A. L., Ochoa W. C., Ophoff R. A., Osiecki L., Pakstis A. J., Pato M. T., Pato C. N., Piacentini J., Pittenger C., Pollak Y., Rauch S. L., Renner T. J., Reus V. I., Richter M. A., Riddle M. A., Robertson M. M., Romero R., Rosario M. C., Rosenberg D., Rouleau G. A., Ruhrmann S., Ruiz-Linares A., Sampaio A. S., Samuels J., Sandor P., Sheppard B., Singer H. S., Smit J. H., Stein D. J., Strengman E., Tischfield J. A., Valencia Duarte A. V., Vallada H., Van Nieuwerburgh F., Veenstra-Vanderweele J., Walitza S., Wang Y., Wendland J. R., Westenberg H. G.M., Shugart Y. Y., Miguel E. C., McMahon W., Wagner M., Nicolini H., Posthuma D., Hanna G. L., Heutink P., Denys D., Arnold P. D., Oostra B. A., Nestadt G., Freimer N. B., Pauls D. L., Wray N. R., Stewart S. E., Mathews C. A., Knowles J. A., Cox N. J. et Scharf J. M. (2013). Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. PloS Genetics, 9, (10), e1003864.

الإتاحة: https://doi.org/10.1371/journal.pgen.1003864Test
https://constellation.uqac.ca/5144/1/Davis2013_Partitioning_the_heritability.pdfTest

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4

دورية أكاديمية

Genome-wide association study of Tourette's syndrome

المصدر: Molecular Psychiatry ; volume 18, issue 6, page 721-728 ; ISSN 1359-4184 1476-5578

مصطلحات موضوعية: Cellular and Molecular Neuroscience, Psychiatry and Mental health, Molecular Biology

الإتاحة: https://doi.org/10.1038/mp.2012.69Test
https://www.nature.com/articles/mp201269.pdfTest
https://www.nature.com/articles/mp201269Test

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5

دورية أكاديمية

Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies

المؤلفون: Yu, D., Sul, J. H., Tsetsos, F., Nawaz, M. S., Huang, A. Y., Zelaya, I., Illmann, C., Budman, C. L., Budman, C., Woods, M., +119 additional authors

المصدر: Journal Articles

مصطلحات موضوعية: Science & Technology, Life Sciences & Biomedicine, Psychiatry, COPY NUMBER VARIANTS, RISK

وصف الملف: application/pdf

العلاقة: https://academicworks.medicine.hofstra.edu/publications/5707Test; https://academicworks.medicine.hofstra.edu/context/publications/article/6708/viewcontent/AmJPsychiatry2019v176p217.pdfTest

الإتاحة: https://doi.org/10.1176/appi.ajp.2018.18070857Test
https://academicworks.medicine.hofstra.edu/publications/5707Test
https://academicworks.medicine.hofstra.edu/context/publications/article/6708/viewcontent/AmJPsychiatry2019v176p217.pdfTest

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6

دورية أكاديمية

Self injurious behaviour in Tourette syndrome: correlates with impulsivity and impulse control

المؤلفون: Mathews, C A, Waller, J, Glidden, D, Lowe, T L, Herrera, L D, Budman, C L, Erenberg, G, Naarden, A, Bruun, R D, Freimer, N B, Reus, V I

مصطلحات موضوعية: Papers

وصف الملف: text/html

العلاقة: http://jnnp.bmj.com/cgi/content/short/75/8/1149Test; http://dx.doi.org/10.1136/jnnp.2003.020693Test

الإتاحة: https://doi.org/10.1136/jnnp.2003.020693Test
http://jnnp.bmj.com/cgi/content/short/75/8/1149Test

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7

دورية أكاديمية

Ecopipam, a D1 receptor antagonist, for treatment of tourette syndrome in children: A randomized, placebo-controlled crossover study

المؤلفون: Gilbert, D. L., Murphy, T. K., Jankovic, J., Budman, C. L., Black, K. J., Kurlan, R. M., Coffman, K. A., McCracken, J. T., Juncos, J., Chipkin, R. E., +1 additional author

المصدر: Journal Articles

مصطلحات موضوعية: Psychiatry

العلاقة: https://academicworks.medicine.hofstra.edu/publications/4045Test

الإتاحة: https://doi.org/10.1002/mds.27457Test
https://academicworks.medicine.hofstra.edu/publications/4045Test

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8

دورية أكاديمية

Prevalence and predictors of hair pulling disorder and excoriation disorder in Tourette syndrome

المؤلفون: Greenberg, E., Tung, E. S., Gauvin, C., Osiecki, L., Yang, K. G., Curley, E., Essa, A., Illmann, C., Budman, C. L., Scharf, J. M., +10 additional authors

المصدر: Journal Articles

وصف الملف: application/pdf

العلاقة: https://academicworks.medicine.hofstra.edu/publications/3986Test; https://academicworks.medicine.hofstra.edu/context/publications/article/4987/viewcontent/EurChildAdolescPsychiatry2018v27p569.pdfTest

الإتاحة: https://doi.org/10.1007/s00787-017-1074-zTest
https://academicworks.medicine.hofstra.edu/publications/3986Test
https://academicworks.medicine.hofstra.edu/context/publications/article/4987/viewcontent/EurChildAdolescPsychiatry2018v27p569.pdfTest

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9

دورية أكاديمية

Genetic and phenotypic overlap of specific obsessive-compulsive and attention-deficit/hyperactive subtypes with Tourette syndrome

المؤلفون: Hirschtritt, M. E., Darrow, S. M., Illmann, C., Osiecki, L., Grados, M., Sandor, P., Dion, Y., King, R. A., Pauls, D., Budman, C. L., Cath, D. C., Greenberg, E., Lyon, G. J., Yu, D., McGrath, L. M., McMahon, W. M., Lee, P. C., Delucchi, K. L., Scharf, J. M., Mathews, C. A.

المصدر: Psychological Medicine ; volume 48, issue 2, page 279-293 ; ISSN 0033-2917 1469-8978

الإتاحة: https://doi.org/10.1017/s0033291717001672Test
https://www.cambridge.org/core/services/aop-cambridge-core/content/view/S0033291717001672Test

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10

دورية أكاديمية

Cross-disorder genome-wide analyses suggest a complex genetic relationship between tourette's syndrome and OCD

المؤلفون: Yu D., Mathews C. A., Scharf J. M., Neale B. M., Davis L. K., Gamazon E. R., Derks E. M., Evans P., Edlund C. K., Crane J., Fagerness J. A., Osiecki L., Gallagher P., Gerber G., Haddad S., Illmann C., McGrath L. M., Mayerfeld C., Arepalli S., Barlassina C., Barr C. L., Bellodi L., Benarroch F., Berrio G. B., Bienvenu O. J., Black D., Bloch M. H., Brentani H., Bruun R. D., Budman C. L., Camarena B., Campbell D. D., Cappi C., Cardona Silgado J. C., Cavallini M. C., Chavira D. A., Chouinard S., Cook E. H., Cookson M. R., Coric V., Cullen B., Cusi D., Delorme R., Denys D., Dion Y., Eapen V., Egberts K., Falkai P., Fernandez T., Fournier E., Garrido H., Geller D., Gilbert D., Girard S. L., Grabe H. J., Grados M. A., Greenberg B. D., Gross-Tsur V., Grunblatt E., Hardy J., Heiman G. A., Hemmings S. M. J., Herrera L. D., Hezel D. M., Hoekstra P. J., Jankovic J., Kennedy J. L., King R. A., Konkashbaev A. I., Kremeyer B., Kurlan R., Lanzagorta N., Leboyer M., Leckman J. F., Lennertz L., Liu C., Lochner C., Lowe T. L., Lupoli S., Macciardi F., Maier W., Manunta P., Marconi M., McCracken J. T., Mesa Restrepo S. C., Moessner R., Moorjani P., Morgan J., Muller H., Murphy D. L., Naarden A. L., Ochoa W. C., Ophoff R. A., Pakstis A. J., Pato M. T., Pato C. N., Piacentini J., Pittenger C., Pollak Y., Rauch S. L., Renner T., Reus V. I., Richter M. A., Riddle M. A., Robertson M. M., Romero R., Rosario M. C., Rosenberg D., Ruhrmann S., Sabatti C., Salvi E., Sampaio A. S., Samuels J., Sandor P., Service S. K., Sheppard B., Singer H. S., Smit J. H., Stein D. J., Strengman E., Tischfield J. A., Turiel M., Valencia Duarte A. V., Vallada H., Veenstra-VanderWeele J., Walitza S., Walkup J., Wang Y., Weale M., Weiss R., Wendland J. R., Westenberg H. G. M., Yao Y., Hounie A. G., Miguel E. C., Nicolini H., Wagner M., Ruiz-Linares A., Cath D. C., McMahon W., Posthuma D., Oostra B. A., Nestadt G., Rouleau G. A., Purcell S., Jenike M. A., Heutink P., Hanna G. L., Conti D. V., Arnold P. D., Freimer N., Stewart S. E., Knowles J. A., Cox N. J., Pauls D. L.

المساهمون: Yu, D., Mathews, C. A., Scharf, J. M., Neale, B. M., Davis, L. K., Gamazon, E. R., Derks, E. M., Evans, P., Edlund, C. K., Crane, J., Fagerness, J. A., Osiecki, L., Gallagher, P., Gerber, G., Haddad, S., Illmann, C., Mcgrath, L. M., Mayerfeld, C., Arepalli, S., Barlassina, C., Barr, C. L., Bellodi, L., Benarroch, F., Berrio, G. B., Bienvenu, O. J., Black, D., Bloch, M. H., Brentani, H., Bruun, R. D., Budman, C. L., Camarena, B., Campbell, D. D., Cappi, C., Cardona Silgado, J. C., Cavallini, M. C., Chavira, D. A., Chouinard, S., Cook, E. H., Cookson, M. R., Coric, V., Cullen, B., Cusi, D., Delorme, R., Denys, D., Dion, Y., Eapen, V., Egberts, K., Falkai, P., Fernandez, T., Fournier, E., Garrido, H., Geller, D., Gilbert, D., Girard, S. L., Grabe, H. J., Grados, M. A., Greenberg, B. D., Gross-Tsur, V., Grunblatt, E., Hardy, J., Heiman, G. A., Hemmings, S. M. J., Herrera, L. D., Hezel, D. M., Hoekstra, P. J., Jankovic, J., Kennedy, J. L., King, R. A., Konkashbaev, A. I., Kremeyer, B., Kurlan, R., Lanzagorta, N., Leboyer, M., Leckman, J. F., Lennertz, L., Liu, C., Lochner, C., Lowe, T. L., Lupoli, S., Macciardi, F., Maier, W., Manunta, P., Marconi, M., Mccracken, J. T., Mesa Restrepo, S. C., Moessner, R., Moorjani, P., Morgan, J., Muller, H., Murphy, D. L., Naarden, A. L., Ochoa, W. C., Ophoff, R. A., Pakstis, A. J., Pato, M. T., Pato, C. N., Piacentini, J., Pittenger, C., Pollak, Y., Rauch, S. L.

مصطلحات موضوعية: Adult, Comorbidity, Female, Genome-Wide Association Study, Humans, Male, Obsessive-Compulsive Disorder, Polymorphism, Single Nucleotide, Psychiatric Status Rating Scales, Severity of Illness Index, Tourette Syndrome

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000347146000013; volume:172; issue:1; firstpage:82; lastpage:93; numberofpages:12; journal:THE AMERICAN JOURNAL OF PSYCHIATRY; http://hdl.handle.net/20.500.11768/110012Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84920191001

الإتاحة: https://doi.org/20.500.11768/110012Test
https://doi.org/10.1176/appi.ajp.2014.13101306Test
https://hdl.handle.net/20.500.11768/110012Test

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