Tatiana Foroud

  • 40289 Citations
  • 101 h-Index
1976 …2021
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Publications 1988 2019

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2009
20 Citations (Scopus)

Bone mineral density variation in men is influenced by sex-specific and non sex-specific quantitative trait loci

Peacock, M., Koller, D. L., Lai, D., Hui, S., Foroud, T. & Econs, M., Sep 2009, In : Bone. 45, 3, p. 443-448 6 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Bone Density
Hip
Siblings
Spine
6 Citations (Scopus)

Differentially expressed genes strongly correlated with femur strength in rats

Alam, I., Sun, Q., Koller, D. L., Liu, L., Liu, Y., Edenberg, H., Li, J., Foroud, T. & Turner, C. H., Oct 2009, In : Genomics. 94, 4, p. 257-262 6 p.

Research output: Contribution to journalArticle

Femur
Quantitative Trait Loci
Genes
Hepatocyte Nuclear Factor 4
NF-kappa B
5 Citations (Scopus)

Epistasis between QTLs for bone density variation in Copenhagen x dark agouti F2 rats

Koller, D. L., Liu, L., Alam, I., Sun, Q., Econs, M., Foroud, T. & Turner, C. H., Mar 2009, In : Mammalian Genome. 20, 3, p. 180-186 7 p.

Research output: Contribution to journalArticle

Bone Density
Quantitative Trait Loci
Genome
Femur
Chromosomes, Human, Pair 15
39 Citations (Scopus)

Evidence for association between polymorphisms in the cannabinoid receptor 1 (CNR1) gene and cannabis dependence

Agrawal, A., Wetherill, L., Dick, D. M., Xuei, X., Hinrichs, A., Hesselbrock, V., Kramer, J., Nurnberger, J., Schuckit, M., Bierut, L. J., Edenberg, H. & Foroud, T., Jul 5 2009, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 150, 5, p. 736-740 5 p.

Research output: Contribution to journalArticle

Marijuana Abuse
Cannabinoid Receptors
Single Nucleotide Polymorphism
Genes
Chromosomes, Human, Pair 15
121 Citations (Scopus)

Family-based association of FKBP5 in bipolar disorder

Willour, V. L., Chen, H., Toolan, J., Belmonte, P., Cutler, D. J., Goes, F. S., Zandi, P. P., Lee, R. S., MacKinnon, D. F., Mondimore, F. M., Schweizer, B., DePaulo, J. R., Gershon, E. S., McMahon, F. J., Potash, J. B., McMahon, F., Steele, J., Pearl, J., Kassem, L., Lopez, V. & 64 others, Potash, J., MacKinnon, D., Miller, E., Toolan, J., Zandi, P., Schulze, T., Nwulia, E., Simpson, S., Nurnberger, J., Miller, M., Bowman, E., Reich, T., Goate, A., Rice, J., DePaulo, J. R., Stine, C., Gershon, E., Kazuba, D., Maxwell, E., Miller, M. J., Bowman, E. S., Rau, N. L., Moe, P. R., Samavedy, N., El-Mallakh, R., Manji, H., Glitz, D. A., Meyer, E. T., Smiley, C., Foroud, T., Flury, L., Dick, D. M., Edenberg, H., Bierut, L., McInnis, M., MacKinnon, D. F., Mondimore, F. M., Potash, J. B., Zandi, P. P., Avramopoulos, D., Payne, J., Berrettini, W., Byerley, W., Vawter, M., Coryell, W., Crowe, R., Badner, J., Liu, C., Sanders, A., Caserta, M., Dinwiddie, S., Nguyen, T., Harakal, D., Kelsoe, J., McKinney, R., Scheftner, W., Kravitz, H. M., Marta, D., Vaughn-Brown, A., Bederow, L., McMahon, F. J., Detera-Wadleigh, S., Austin, L. & Murphy, D. L., Mar 2009, In : Molecular Psychiatry. 14, 3, p. 261-268 8 p.

Research output: Contribution to journalArticle

Bipolar Disorder
Single Nucleotide Polymorphism
Genetic Models
Glucocorticoid Receptors
Antidepressive Agents
33 Citations (Scopus)

Family-based association of YWHAH in psychotic bipolar disorder

Grover, D., Verma, R., Goes, F. S., Belmonte Mahon, P. L., Gershon, E. S., McMahon, F. J., Potash, J. B., McMahon, F. J., Steele, J., Pearl, J., Kassem, L., Lopez, V., Schulze, T., Potash, J., MacKinnon, D., Miller, E., Toolan, J., Zandi, P., Simpson, S., Nurnberger, J. & 64 others, Miller, M., Bowman, E., Reich, T., Goate, A., Rice, J., DePaulo, J. R., Simpson, S., Stine, C., Gershon, E., Kazuba, D., Maxwell, E., Nurnberger, J., Miller, M. J., Bowman, E. S., Rau, N. L., Moe, P. R., Samavedy, N., El-Mallakh, R., Manji, H., Glitz, D. A., Meyer, E. T., Smiley, C., Foroud, T., Flury, L., Dick, D. M., Edenberg, H., Rice, J., Reich, T., Goate, A., Bierut, L., McInnis, M., DePaulo, J. R., MacKinnon, D. F., Mondimore, F. M., Potash, J. B., Zandi, P. P., Avramopoulos, D., Payne, J., Berrettini, W., Byerley, W., Vawter, M., Coryell, W., Crowe, R., Gershon, E., Badner, J., McMahon, F., Liu, C., Sanders, A., Caserta, M., Dinwiddie, S., Nguyen, T., Harakal, D., Kelsoe, J., McKinney, R., Scheftner, W., Kravitz, H. M., Marta, D., Vaughn-Brown, A., Bederow, L., McMahon, F., Kassem, L., Detera-Wadleigh, S., Austin, L. & Murphy, D. L., Oct 5 2009, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 150, 7, p. 977-983 7 p.

Research output: Contribution to journalArticle

Bipolar Disorder
Psychotic Disorders
Schizophrenia
Single Nucleotide Polymorphism
Chromosome Disorders
24 Citations (Scopus)

From QTL to candidate gene: A genetic approach to alcoholism research

Spence, J. P., Liang, T., Liu, L., Johnson, P., Foroud, T., Carr, L. G. & Shekhar, A., Jun 2009, In : Current Drug Abuse Reviews. 2, 2, p. 127-134 8 p.

Research output: Contribution to journalArticle

Alcoholism
Research
Alcohol Drinking
Genes
Alcohol-Related Disorders
21 Citations (Scopus)

Genome screen in familial intracranial aneurysm.

Foroud, T., Sauerbeck, L., Brown, R., Anderson, C., Woo, D., Kleindorfer, D., Flaherty, M. L., Deka, R., Hornung, R., Meissner, I., Bailey-Wilson, J. E., Langefeld, C., Rouleau, G., Connolly, E. S., Lai, D., Koller, D. L., Huston, J. & Broderick, J. P., 2009, In : BMC Medical Genetics. 10, p. 3 1 p.

Research output: Contribution to journalArticle

Intracranial Aneurysm
Genome
Chromosomes
Smoking
Diagnostic Imaging
12 Citations (Scopus)

Genome screen to detect linkage to common susceptibility genes for intracranial and aortic aneurysms

Worrall, B. B., Foroud, T., Brown, R. D., Connolly, E. S., Hornung, R. W., Huston, J., Kleindorfer, D., Koller, D. L., Lai, D., Moomaw, C. J., Sauerbeck, L., Woo, D. & Broderick, J. P., Jan 1 2009, In : Stroke. 40, 1, p. 71-76 6 p.

Research output: Contribution to journalArticle

Aortic Aneurysm
Intracranial Aneurysm
Genome
Thoracic Aortic Aneurysm
Genes
58 Citations (Scopus)

Genomewide association study for onset age in Parkinson disease

Latourelle, J. C., Pankratz, N., Dumitriu, A., Wilk, J. B., Goldwurm, S., Pezzoli, G., Mariani, C. B., DeStefano, A. L., Halter, C., Gusella, J. F., Nichols, W. C., Myers, R. H. & Foroud, T., Sep 22 2009, In : BMC Medical Genetics. 10, p. 98 1 p., 1471.

Research output: Contribution to journalArticle

Age of Onset
Parkinson Disease
Single Nucleotide Polymorphism
Genes
Meta-Analysis
290 Citations (Scopus)

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

Pankratz, N., Wilk, J. B., Latourelle, J. C., DeStefano, A. L., Halter, C., Pugh, E. W., Doheny, K. F., Gusella, J. F., Nichols, W. C., Foroud, T. & Myers, R. H., 2009, In : Human Genetics. 124, 6, p. 593-605 13 p.

Research output: Contribution to journalArticle

Parkinson Disease
Genes
Disease Susceptibility
Chromosomes, Human, Pair 4
Single Nucleotide Polymorphism
234 Citations (Scopus)

Genome-wide association study of bipolar disorder in European American and African American individuals

Smith, E. N., Bloss, C. S., Badner, J. A., Barrett, T., Belmonte, P. L., Berrettini, W., Byerley, W., Coryell, W., Craig, D., Edenberg, H., Eskin, E., Foroud, T., Gershon, E., Greenwood, T. A., Hipolito, M., Koller, D. L., Lawson, W. B., Liu, C., Lohoff, F., McInnis, M. G. & 17 others, McMahon, F. J., Mirel, D. B., Murray, S. S., Nievergelt, C., Nurnberger, J., Nwulia, E. A., Paschall, J., Potash, J. B., Rice, J., Schulze, T. G., Scheftner, W., Panganiban, C., Zaitlen, N., Zandi, P. P., Zöllner, S., Schork, N. J. & Kelsoe, J. R., Aug 2009, In : Molecular Psychiatry. 14, 8, p. 755-763 9 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Bipolar Disorder
African Americans
Single Nucleotide Polymorphism
Intergenic DNA
15 Citations (Scopus)

Genomewide SNP screen to detect quantitative trait loci for alcohol preference in the high alcohol preferring and low alcohol preferring mice

Bice, P., Valdar, W., Zhang, L., Liu, L., Lai, D., Grahame, N., Flint, J., Li, T. K., Lumeng, L. & Foroud, T., Mar 2009, In : Alcoholism: Clinical and Experimental Research. 33, 3, p. 531-537 7 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Single Nucleotide Polymorphism
Genes
Alcohols
Chromosomes
86 Citations (Scopus)

Greater rupture risk for familial as compared to sporadic unruptured intracranial aneurysms

Broderick, J. P., Brown, R. D., Sauerbeck, L., Hornung, R., Huston, J., Woo, D., Anderson, C., Rouleau, G., Kleindorfer, D., Flaherty, M. L., Meissner, I., Foroud, T., Moomaw, E. C. J. & Connolly, E. S., Jun 1 2009, In : Stroke. 40, 6, p. 1952-1957 6 p.

Research output: Contribution to journalArticle

Intracranial Aneurysm
Rupture
Angiography
Cerebral Angiography
Ruptured Aneurysm
39 Citations (Scopus)

Multiple step pattern as a biomarker in Parkinson disease

Blekher, T., Weaver, M., Rupp, J., Nichols, W. C., Hui, S., Gray, J., Yee, R. D., Wojcieszek, J. & Foroud, T., Aug 2009, In : Parkinsonism and Related Disorders. 15, 7, p. 506-510 5 p.

Research output: Contribution to journalArticle

Parkinson Disease
Biomarkers
Saccades
Siblings
Aptitude
120 Citations (Scopus)

Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset

Nichols, W. C., Pankratz, N., Marek, D. K., Pauciulo, M. W., Elsaesser, V. E., Halter, C. A., Rudolph, A., Wojcieszek, J., Pfeiffer, R. F. & Foroud, T., Jan 27 2009, In : Neurology. 72, 4, p. 310-316 7 p.

Research output: Contribution to journalArticle

Glucosylceramidase
Disease Susceptibility
Age of Onset
Parkinson Disease
Mutation
47 Citations (Scopus)

Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations

Pankratz, N., Kissell, D. K., Pauciulo, M. W., Halter, C. A., Rudolph, A., Pfeiffer, R. F., Marder, K. S., Foroud, T. & Nichols, W. C., Jul 2009, In : Neurology. 73, 4, p. 279-286 8 p.

Research output: Contribution to journalArticle

Parkinson Disease
Virulence
Mutation
Haploinsufficiency
Age of Onset
9 Citations (Scopus)

Premenstrual mood symptoms: Study of familiality and personality correlates in mood disorder pedigrees

NIMH Genetics Initiative Bipolar Disorder Consortium, Feb 1 2009, In : Archives of Women's Mental Health. 12, 1, p. 27-34 8 p.

Research output: Contribution to journalArticle

Pedigree
Mood Disorders
Personality
Bipolar Disorder
Major Depressive Disorder
113 Citations (Scopus)

Singleton deletions throughout the genome increase risk of bipolar disorder

Zhang, D., Cheng, L., Qian, Y., Alliey-Rodriguez, N., Kelsoe, J. R., Greenwood, T., Nievergelt, C., Barrett, T. B., McKinney, R., Schork, N., Smith, E. N., Bloss, C., Nurnberger, J., Edenberg, H., Foroud, T., Sheftner, W., Lawson, W. B., Nwulia, E. A., Hipolito, M., Coryell, W. & 16 others, Rice, J., Byerley, W., McMahon, F., Schulze, T. G., Berrettini, W., Potash, J. B., Belmonte, P. L., Zandi, P. P., McInnis, M. G., Zöllner, S., Craig, D., Szelinger, S., Koller, D., Christian, S. L., Liu, C. & Gershon, E. S., Apr 2009, In : Molecular Psychiatry. 14, 4, p. 376-380 5 p.

Research output: Contribution to journalArticle

Bipolar Disorder
Genome
Single Nucleotide Polymorphism
Genomic Structural Variation
Age of Onset
19 Citations (Scopus)

Test-retest reliability of saccadic measures in subjects at risk for Huntington disease

Blekher, T., Weaver, M. R., Cai, X., Hui, S., Marshall, J., Jackson, J. G., Wojcieszek, J., Yee, R. D. & Foroud, T., Dec 2009, In : Investigative Ophthalmology and Visual Science. 50, 12, p. 5707-5711 5 p.

Research output: Contribution to journalArticle

Saccades
Huntington Disease
Reproducibility of Results
Biomarkers
Eye Movements
33 Citations (Scopus)

Variation in GIGYF2 is not associated with Parkinson disease

Nichols, W. C., Kissell, D. K., Pankratz, N., Pauciulo, M. W., Elsaesser, V. E., Clark, K. A., Halter, C. A., Rudolph, A., Wojcieszek, J., Pfeiffer, R. F. & Foroud, T., Jun 2 2009, In : Neurology. 72, 22, p. 1886-1892 7 p.

Research output: Contribution to journalArticle

Parkinson Disease
Chromosomes
Mutation
Genes
13 Citations (Scopus)

Visual scanning and cognitive performance in prediagnostic and early-stage Huntington's disease

Blekher, T., Weaver, M. R., Marshall, J., Hui, S., Jackson, J. G., Stout, J. C., Beristain, X., Wojcieszek, J., Yee, R. D. & Foroud, T., Mar 15 2009, In : Movement Disorders. 24, 4, p. 533-540 8 p.

Research output: Contribution to journalArticle

Huntington Disease
Eye Movements
Genes
2008
65 Citations (Scopus)

Analyses of the national institute on aging late-onset Alzheimer's disease family study: Implication of additional loci

Lee, J. H., Cheng, R., Graff-Radford, N., Foroud, T. & Mayeux, R., Nov 2008, In : Archives of Neurology. 65, 11, p. 1518-1526 9 p.

Research output: Contribution to journalArticle

National Institute on Aging (U.S.)
Alzheimer Disease
Genetic Loci
Onset
Alzheimer's Disease
4 Citations (Scopus)

A novel non-parametric regression reveals linkage on chromosome 4 for the number of externalizing symptoms in sib-pairs

Ghosh, S., Bierut, L. J., Porjesz, B., Edenberg, H., Dick, D., Goate, A., Hesselbrock, V., Nurnberger, J., Foroud, T., Kramer, J., Rice, J. & Begleiter, H., Oct 5 2008, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 147, 7, p. 1301-1305 5 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 4
Alcoholism
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 1
Multigene Family
55 Citations (Scopus)

A regulatory variation in OPRK1, the gene encoding the κ-opioid receptor, is associated with alcohol dependence

Edenberg, H., Wang, J., Tian, H., Pochareddy, S., Xuei, X., Wetherill, L., Goate, A., Hinrichs, T., Kuperman, S., Nurnberger, J., Schuckit, M., Tischfield, J. A. & Foroud, T., Jun 15 2008, In : Human Molecular Genetics. 17, 12, p. 1783-1789 7 p.

Research output: Contribution to journalArticle

Opioid Receptors
Alcoholism
Genes
Transcription Initiation Site
DNA Sequence Analysis
34 Citations (Scopus)

Association analysis of genes encoding the nociceptin receptor (OPRL1) and its endogenous ligand (PNOC) with alcohol or illicit drug dependence

Xuei, X., Flury-Wetherill, L., Almasy, L., Bierut, L., Tischfield, J., Schuckit, M., Nurnberger, J., Foroud, T. & Edenberg, H., Mar 2008, In : Addiction Biology. 13, 1, p. 80-87 8 p.

Research output: Contribution to journalArticle

Street Drugs
Substance-Related Disorders
Single Nucleotide Polymorphism
Alcohols
Ligands
69 Citations (Scopus)

Association of NFKB1, which encodes a subunit of the transcription factor NF-κB, with alcohol dependence

Edenberg, H., Xuei, X., Wetherill, L. F., Bierut, L., Bucholz, K., Dick, D. M., Hesselbrock, V., Kuperman, S., Porjesz, B., Schuckit, M. A., Tischfield, J. A., Almasy, L. A., Nurnberger, J. & Foroud, T., Apr 1 2008, In : Human Molecular Genetics. 17, 7, p. 963-970 8 p.

Research output: Contribution to journalArticle

Alcoholism
Transcription Factors
Single Nucleotide Polymorphism
Genes
Alcoholics
10 Citations (Scopus)

Association studies of ALOX5 and bone mineral density in healthy adults

Foroud, T., Ichikawa, S., Koller, D., Lai, D., Curry, L., Xuei, X., Edenberg, H., Hui, S., Peacock, M. & Econs, M., May 2008, In : Osteoporosis International. 19, 5, p. 637-643 7 p.

Research output: Contribution to journalArticle

Bone Density
Single Nucleotide Polymorphism
Siblings
Arachidonate 5-Lipoxygenase
Femur Neck
36 Citations (Scopus)

A Systematic Single Nucleotide Polymorphism Screen to Fine-Map Alcohol Dependence Genes on Chromosome 7 Identifies Association With a Novel Susceptibility Gene ACN9

Dick, D. M., Aliev, F., Wang, J. C., Saccone, S., Hinrichs, A., Bertelsen, S., Budde, J., Saccone, N., Foroud, T., Nurnberger, J., Xuei, X., Conneally, P. M., Schuckit, M., Almasy, L., Crowe, R., Kuperman, S., Kramer, J., Tischfield, J. A., Hesselbrock, V., Edenberg, H. & 4 others, Porjesz, B., Rice, J. P., Bierut, L. & Goate, A., Jun 1 2008, In : Biological Psychiatry. 63, 11, p. 1047-1053 7 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 7
Alcoholism
Single Nucleotide Polymorphism
Genes
HapMap Project
25 Citations (Scopus)

Automated diagnosis of fetal alcohol syndrome using 3D facial image analysis

Fang, S., McLaughlin, J., Fang, J., Huang, J., Autti-Rämö, I., Fagerlund, Å., Jacobson, S. W., Robinson, L. K., Hoyme, H. E., Mattson, S. N., Riley, E., Zhou, F., Ward, R., Moore, E. S. & Foroud, T., Aug 2008, In : Orthodontics and Craniofacial Research. 11, 3, p. 162-171 10 p.

Research output: Contribution to journalArticle

Fetal Alcohol Spectrum Disorders
Lasers
Alcohols
Computer Graphics
Finland
5 Citations (Scopus)

CLCN7 polymorphisms and bone mineral density in healthy premenopausal white women and in white men

Chu, K., Koller, D. L., Ichikawa, S., Snyder, R., Curry, L., Lai, D., Austin, A., Xuei, X., Edenberg, H., Hui, S., Foroud, T., Peacock, M. & Econs, M., Dec 2008, In : Bone. 43, 6, p. 995-998 4 p.

Research output: Contribution to journalArticle

Chloride Channels
Bone Density
Genes
Femur Neck
Osteopetrosis
26 Citations (Scopus)

Clinical correlates of depressive symptoms in familial Parkinson's disease

Pankratz, N., Marder, K. S., Halter, C. A., Rudolph, A., Shults, C. W., Nichols, W. C. & Foroud, T., Nov 15 2008, In : Movement Disorders. 23, 15, p. 2216-2223 8 p.

Research output: Contribution to journalArticle

Parkinson Disease
Depression
Geriatrics
Activities of Daily Living
Logistic Models
28 Citations (Scopus)

Detection of dental fluorosis-associated quantitative trait loci on mouse chromosomes 2 and 11

Everett, E. T., Yan, D., Weaver, M., Liu, L., Foroud, T. & Martinez Mier, E., Dec 2008, In : Cells Tissues Organs. 189, 1-4, p. 212-218 7 p.

Research output: Contribution to journalArticle

Dental Fluorosis
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 2
Quantitative Trait Loci
Dental Enamel
9 Citations (Scopus)
Genome
Osteoporotic Fractures
Quantitative Trait Loci
Chromosomes, Human, Pair 20
Chromosomes, Human, Pair 15
42 Citations (Scopus)

Evidence of association between brain-derived neurotrophic factor gene and bipolar disorder

Liu, L., Foroud, T., Xuei, X., Berrettini, W., Byerley, W., Coryell, W., El-Mallakh, R., Gershon, E. S., Kelsoe, J. R., Lawson, W. B., MacKinnon, D. F., McInnis, M., McMahon, F. J., Murphy, D. L., Rice, J., Scheftner, W., Zandi, P. R., Lohoff, F. W., Niculescu, A., Meyer, E. T. & 2 others, Edenberg, H. & Nurnberger, J., Dec 2008, In : Psychiatric Genetics. 18, 6, p. 267-274 8 p.

Research output: Contribution to journalArticle

Brain-Derived Neurotrophic Factor
Bipolar Disorder
Single Nucleotide Polymorphism
Genes
Mood Disorders
10 Citations (Scopus)

Genetic loci affecting bone structure and strength in inbred COP and DA rats

Sun, Q., Alam, I., Liu, L., Koller, D. L., Carr, L. G., Econs, M., Foroud, T. & Turner, C. H., Mar 2008, In : Bone. 42, 3, p. 547-553 7 p.

Research output: Contribution to journalArticle

Genetic Loci
Lumbar Vertebrae
Femur
Bone and Bones
Genome
39 Citations (Scopus)

Genome screen to detect linkage to intracranial aneurysm susceptibility genes: The familial intracranial aneurysm (FIA) study

Foroud, T., Sauerbeck, L., Brown, R., Anderson, C., Woo, D., Kleindorfer, D., Flaherty, M. L., Deka, R., Hornung, R., Meissner, I., Bailey-Wilson, J. E., Rouleau, G., Connolly, E. S., Lai, D., Koller, D. L., Huston, J. & Broderick, J. P., May 1 2008, In : Stroke. 39, 5, p. 1434-1440 7 p.

Research output: Contribution to journalArticle

Intracranial Aneurysm
Genome
Smoking
Chromosomes, Human, Pair 4
Genes
11 Citations (Scopus)

Genome-wide parametric linkage analyses of 644 bipolar pedigrees suggest susceptibility loci at chromosomes 16 and 20

Ross, J., Berrettini, W., Coryell, W., Gershon, E. S., Badner, J. A., Kelsoe, J. R., McInnis, M. G., McMahon, F. J., Murphy, D. L., Nurnberger, J., Foroud, T., Rice, J. P., Scheftner, W. B., Zandi, P., Edenberg, H. & Byerley, W., Aug 2008, In : Psychiatric Genetics. 18, 4, p. 191-198 8 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 20
Chromosomes, Human, Pair 16
Pedigree
Genome
Bipolar Disorder
10 Citations (Scopus)

Genomic expression analysis of rat chromosome 4 for skeletal traits at femoral neck

Alam, I., Sun, Q., Liu, L., Koller, D. L., Liu, Y., Edenberg, H., Econs, M., Foroud, T. & Turner, C. H., Oct 2008, In : Physiological Genomics. 35, 2, p. 191-196 6 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 4
Femur Neck
Quantitative Trait Loci
Inbred F344 Rats
Hip Fractures
4 Citations (Scopus)

Identification of a linkage disequilibrium block in chromosome 1q associated with BMD in premenopausal white women

Ichikawa, S., Koller, D. L., Curry, L. R., Lai, D., Xuei, X., Pugh, E. W., Tsai, Y. Y., Doheny, K. F., Edenberg, H., Hui, S., Foroud, T., Peacock, M. & Econs, M., Oct 2008, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 23, 10, p. 1680-1688 9 p.

Research output: Contribution to journalArticle

Linkage Disequilibrium
Chromosomes
Single Nucleotide Polymorphism
Genes
Spine
14 Citations (Scopus)

Inheritance of susceptibility to root resorption associated with orthodontic force in mice

Abass, S. K., Hartsfield, J. K., Al-Qawasmi, R. A., Everett, E. T., Foroud, T. & Roberts, W. E., Dec 2008, In : American Journal of Orthodontics and Dentofacial Orthopedics. 134, 6, p. 742-750 9 p.

Research output: Contribution to journalArticle

Root Resorption
Orthodontics
Multifactorial Inheritance
Inheritance Patterns
Genetic Heterogeneity
51 Citations (Scopus)

Linkage scan for quantitative traits identifies new regions of interest for substance dependence in the Collaborative Study on the Genetics of Alcoholism (COGA) sample

Agrawal, A., Hinrichs, A. L., Dunn, G., Bertelsen, S., Dick, D. M., Saccone, S. F., Saccone, N. L., Grucza, R. A., Wang, J. C., Cloninger, C. R., Edenberg, H., Foroud, T., Hesselbrock, V., Kramer, J., Bucholz, K. K., Kuperman, S., Nurnberger, J., Porjesz, B., Schuckit, M. A., Goate, A. M. & 1 others, Bierut, L. J., Jan 11 2008, In : Drug and Alcohol Dependence. 93, 1-2, p. 12-20 9 p.

Research output: Contribution to journalArticle

alcoholism
Alcoholism
Substance-Related Disorders
drug dependence
alcohol
7 Citations (Scopus)

Linkage screen for BMD phenotypes in male and female COP and DA rat strains

Koller, D. L., Liu, L., Alam, I., Sun, Q., Econs, M., Foroud, T. & Turner, C. H., Sep 2008, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 23, 9, p. 1382-1388 7 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Phenotype
Chromosomes, Human, Pair 1
Femur
Inbred Strains Animals
83 Citations (Scopus)

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease

Haugarvoll, K., Rademakers, R., Kachergus, J. M., Nuytemans, K., Ross, O. A., Gibson, J. M., Tan, E. K., Gaig, C., Tolosa, E., Goldwurm, S., Guidi, M., Riboldazzi, G., Brown, L., Walter, U., Benecke, R., Berg, D., Gasser, T., Theuns, J., Pals, P., Cras, P. & 14 others, De Deyn, P. P., Engelborghs, S., Pickut, B., Uitti, R. J., Foroud, T., Nichols, W. C., Hagenah, J., Klein, C., Samii, A., Zabetian, C. P., Bonifati, V., Van Broeckhoven, C., Farrer, M. J. & Wszolek, Z. K., Apr 2008, In : Neurology. 70, 16 PART 2, p. 1456-1460 5 p.

Research output: Contribution to journalArticle

Parkinsonian Disorders
Parkinson Disease
Age of Onset
Leucine
Mutation
58 Citations (Scopus)

Neuropeptide Y receptor genes are associated with alcohol dependence, alcohol withdrawal phenotypes, and cocaine dependence

Wetherill, L., Schuckit, M. A., Hesselbrock, V., Xuei, X., Liang, T., Dick, D. M., Kramer, J., Nurnberger, J., Tischfield, J. A., Porjesz, B., Edenberg, H. & Foroud, T., Dec 2008, In : Alcoholism: Clinical and Experimental Research. 32, 12, p. 2031-2040 10 p.

Research output: Contribution to journalArticle

Neuropeptide Y Receptors
Cocaine-Related Disorders
Cocaine
Alcoholism
Genes

Reply from the Authors

Nichols, W. C., Elsaesser, V. E., Pankratz, N., Pauciulo, M. W., Marek, D. K., Halter, C. A., Rudolph, A. & Foroud, T., Jun 10 2008, In : Neurology. 70, 24, p. 2348-2349 2 p.

Research output: Contribution to journalArticle

Response

Brown, R. D., Huston, J., Hornung, R., Foroud, T., Kallmes, D. F., Kleindorfer, D., Meissner, I., Woo, D., Sauerbeck, L. & Broderick, J., Jun 2008, In : Journal of Neurosurgery. 108, 6, p. 1131 1 p.

Research output: Contribution to journalArticle

54 Citations (Scopus)

Screening for brain aneurysm in the Familial Intracranial Aneurysm study: Frequency and predictors of lesion detection

Brown, R. D., Huston, J., Hornung, R., Foroud, T., Kallmes, D. F., Kleindorfer, D., Meissner, I., Woo, D., Sauerbeck, L. & Broderick, J., Jun 2008, In : Journal of Neurosurgery. 108, 6, p. 1132-1138 7 p.

Research output: Contribution to journalArticle

Intracranial Aneurysm
Aneurysm
Magnetic Resonance Angiography
Smoking
Odds Ratio
9 Citations (Scopus)
Genetic Loci
Quantitative Trait Loci
Femur Neck
Bone and Bones
Chromosomes, Human, Pair 1
43 Citations (Scopus)

Ten-year rate of longitudinal change in neurocognitive and motor function in prediagnosis Huntington disease

Solomon, A. C., Stout, J. C., Weaver, M., Queller, S., Tomusk, A., Whitlock, K. B., Hui, S., Marshall, J., Jackson, J. G., Siemens, E. R., Beristain, X., Wojcieszek, J. & Foroud, T., Oct 15 2008, In : Movement Disorders. 23, 13, p. 1830-1836 7 p.

Research output: Contribution to journalArticle

Huntington Disease
Age of Onset
Longitudinal Studies