Tatiana Foroud

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

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2005
24 Citations (Scopus)

Genome screen for bone mineral density phenotypes in Fisher 344 and Lewis rat strains

Koller, D. L., Alam, I., Sun, Q., Liu, L., Fishburn, T., Carr, L. G., Econs, M., Foroud, T. & Turner, C. H., Aug 2005, In : Mammalian Genome. 16, 8, p. 578-586 9 p.

Research output: Contribution to journalArticle

Bone Density
Genome
Phenotype
Inbred Lew Rats
Spine
13 Citations (Scopus)

LRRK2: Both a cause and a risk factor for Parkinson disease?

Foroud, T., Sep 13 2005, In : Neurology. 65, 5, p. 664-665 2 p.

Research output: Contribution to journalArticle

Parkinson Disease
29 Citations (Scopus)

No association of the GABAA receptor genes on chromosome 5 with alcoholism in the collaborative study on the genetics of alcoholism sample

Dick, D. M., Edenberg, H., Xuei, X., Goate, A., Hesselbrock, V., Schuckit, M., Crowe, R. & Foroud, T., Jan 5 2005, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 132 B, 1, p. 24-28 5 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 5
GABA-A Receptors
Alcoholism
Genes
Alcohol-Related Disorders
40 Citations (Scopus)

Polymorphisms in the estrogen receptor β (ESR2) gene are associated with bone mineral density in Caucasian men and women

Ichikawa, S., Koller, D. L., Peacock, M., Johnson, M. L., Lai, D., Hui, S., Johnston, C. C., Foroud, T. & Econs, M., Nov 2005, In : Journal of Clinical Endocrinology and Metabolism. 90, 11, p. 5921-5927 7 p.

Research output: Contribution to journalArticle

Polymorphism
Estrogen Receptors
Bone Density
Minerals
Bone
58 Citations (Scopus)

Relationship of age of first drink to child behavioral problems and family psychopathology

Kuperman, S., Chan, G., Kramer, J. R., Bierut, L., Bucholz, K. K., Fox, L., Hesselbrock, V., Nurnberger, J., Reich, T., Reich, W., Schuckit, M. A., Edenberg, H., Connealfy, P. M., Foroud, T., Crowe, R., Porjesz, B., Begleiter, H., Rice, J., Goate, A., Taylor, R. & 2 others, Tischfield, J. & Almasy, L., Oct 2005, In : Alcoholism: Clinical and Experimental Research. 29, 10, p. 1869-1876 8 p.

Research output: Contribution to journalArticle

Psychopathology
Alcoholism
Alcohols
Antisocial Personality Disorder
Child Behavior
59 Citations (Scopus)

Sex-specific and non-sex-specific quantitative trait loci contribute to normal variation in bone mineral density in men

Peacock, M., Koller, D. L., Fishburn, T., Krishnan, S., Lai, D., Hui, S., Johnston, C. C., Foroud, T. & Econs, M., May 2005, In : Journal of Clinical Endocrinology and Metabolism. 90, 5, p. 3060-3066 7 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Bone Density
Minerals
Bone
Spine
32 Citations (Scopus)

Sex-specific quantitative trait loci contribute to normal variation in bone structure at the proximal femur in men

Peacock, M., Koller, D. L., Lai, D., Hui, S., Foroud, T. & Econs, M., Oct 2005, In : Bone. 37, 4, p. 467-473 7 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Femur
Bone and Bones
Chromosomes
Thigh
1 Citation (Scopus)

Standard linkage and association methods identify the mechanism of four susceptibility genes for a simulated complex disease

Pankratz, N., Edenberg, E. & Foroud, T., Dec 30 2005, In : BMC Genetics. 6, SUPPL.1, S142.

Research output: Contribution to journalArticle

Single Nucleotide Polymorphism
Chromosomes, Human, Pair 3
Genes
Chromosomes, Human, Pair 1
Phenotype
47 Citations (Scopus)

The Familial Intracranial Aneurysm (FIA) study protocol

Broderick, J. P., Sauerbeck, L. R., Foroud, T., Huston, J., Pankratz, N., Meissner, I. & Brown, R. D., Apr 26 2005, In : BMC Medical Genetics. 6, 17.

Research output: Contribution to journalArticle

Intracranial Aneurysm
Ruptured Aneurysm
Aneurysm
Rupture
Genome
52 Citations (Scopus)

The North American Multiple System Atrophy Study Group

Gilman, S., May, S. J., Shults, C. W., Tanner, C. M., Kukull, W., Lee, V. M. Y., Masliah, E., Low, P., Sandroni, P., Trojanowski, J. Q., Ozelius, L. & Foroud, T., Dec 2005, In : Journal of Neural Transmission. 112, 12, p. 1687-1694 8 p.

Research output: Contribution to journalArticle

Multiple System Atrophy
alpha-Synuclein
Levodopa
Research Personnel
Cerebellar Diseases
28 Citations (Scopus)

Whole-genome scan for linkage to bone strength and structure in inbred Fischer 344 and Lewis rats

Alam, I., Sun, Q., Liu, L., Koller, D. L., Fishburn, T., Carr, L. G., Econs, M., Foroud, T. & Turner, C. H., Sep 2005, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 20, 9, p. 1589-1596 8 p.

Research output: Contribution to journalArticle

Inbred Lew Rats
Inbred F344 Rats
Genome
Femur
Bone and Bones
2004
67 Citations (Scopus)

A genome-wide screen for genes influencing conduct disorder

Dick, D. M., Li, T. K., Edenberg, H., Hesselbrock, V., Kramer, J., Kuperman, S., Porjesz, B., Bucholz, K., Goate, A., Nurnberger, J. & Foroud, T., 2004, In : Molecular Psychiatry. 9, 1, p. 81-86 6 p.

Research output: Contribution to journalArticle

Conduct Disorder
Genome
Genes
Alcoholism
Chromosomes, Human, Pair 2
101 Citations (Scopus)

A Genomic Scan for Habitual Smoking in Families of Alcoholics: Common and Specific Genetic Factors in Substance Dependence

Bierut, L. J., Rice, J. P., Goate, A., Hinrichs, A. L., Saccone, N. L., Foroud, T., Edenberg, H., Cloninger, C. R., Begleiter, H., Conneally, P. M., Crowe, R. R., Hesselbrock, V., Li, T. K., Nurnberger, J., Porjesz, B., Schuckit, M. A. & Reich, T., Jan 1 2004, In : American Journal of Medical Genetics. 124 A, 1, p. 19-27 9 p.

Research output: Contribution to journalArticle

Alcoholics
Substance-Related Disorders
Alcoholism
Smoking
Chromosomes, Human, Pair 2
113 Citations (Scopus)

Association of GABRG3 with Alcohol Dependence

Dick, D. M., Edenberg, H., Xuei, X., Goate, A., Kuperman, S., Schuckit, M., Crowe, R., Smith, T. L., Porjesz, B., Begleiter, H. & Foroud, T., Jan 2004, In : Alcoholism: Clinical and Experimental Research. 28, 1, p. 4-9 6 p.

Research output: Contribution to journalArticle

Alcoholism
Genes
Alcohols
GABA-A Receptors
Chromosomes
47 Citations (Scopus)

Confirmation of Linkage to Chromosome 1q for Peak Vertebral Bone Mineral Density in Premenopausal White Women

Econs, M., Koller, D. L., Hui, S., Fishburn, T., Conneally, P. M., Johnston, C. C., Peacock, M. & Foroud, T., Feb 2004, In : American Journal of Human Genetics. 74, 2, p. 223-228 6 p.

Research output: Contribution to journalArticle

Bone Density
Chromosomes
Spine
Siblings
Microsatellite Repeats
32 Citations (Scopus)

Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease

Nichols, W. C., Uniacke, S. K., Pankratz, N., Reed, T., Simon, D. K., Halter, C., Rudolph, A., Shults, C. W., Conneally, P. M., Foroud, T., Wojcieszek, J., Belden, J., Carter, J., Camicioli, R., Andrews, P., Panisset, M., Hall, J., Hubble, J., Fernandez, M., Reider, C. & 79 others, Rajput, A., Rajput, A., Shirley, T., Mendis, T., Grimes, D. A., Gray, P., Ramos, C. S., Roque, S., Pfeiffer, R., Pfeiffer, B., Elmer, L., Davis, K., Friedman, J., Fernandez, H., Lannon, M., Reich, S., Dunlop, B., Seeberger, L., O'Brien, C., Judd, D., Hauser, R., Zesiewicz, T., Delgado, H., Shults, C., Fontaine, D., Jennings, D., Marek, K., Mendick, S., Aminoff, M., DiMinno, M., Lewitt, P., DeAngelis, M., Pahwa, R., Thomas, S., Truong, D., Pathak, M., Tran, A., Rodnitzky, R., Dobson, J., Koller, W., Weiner, W., Lyons, K., Kurlan, R., Berry, D., Bertoni, J., Peterson, C., Martin, W., Tuite, P., Schacherer, R., Marder, K., Harris, J., Jankovic, J., Hunter, C., Lang, A., Kleimer-Fisman, G., Nieves, A., So, J., Factor, S., Evans, S., Manyam, B., Wulbrecht, B., Walker, F., Hunt, V., Gordon, M. F., Hamman, J., Kang, U. J., Young, J., Blindauer, K., Petit, J., Rao, J., Cook, M., Stacy, M., Williamson, K., Pullman, R. S., Boyar, K., Leehey, M., Derian, T., Gordon, P. & Werner, J., Jun 2004, In : Movement Disorders. 19, 6, p. 649-655 7 p.

Research output: Contribution to journalArticle

Parkinson Disease
Introns
Genes
DNA Restriction Enzymes
Age of Onset
17 Citations (Scopus)
Femur Neck
Alleles
Gene Frequency
Population
Genetic Markers
32 Citations (Scopus)

Genes influencing Parkinson disease onset: Replication of PARK3 and identification of novel loci

Pankratz, N., Uniacke, S. K., Halter, C. A., Rudolph, A., Shults, C. W., Conneally, P. M., Foroud, T. & Nichols, W. C., May 11 2004, In : Neurology. 62, 9, p. 1616-1618 3 p.

Research output: Contribution to journalArticle

Parkinson Disease
Chromosomes
Disease Susceptibility
Genes
Genome
31 Citations (Scopus)

Genetics of Parkinson Disease

Pankratz, N. & Foroud, T., Apr 2004, In : NeuroRx. 1, 2, p. 235-242 8 p.

Research output: Contribution to journalArticle

Inborn Genetic Diseases
Parkinson Disease
Genes
Mutation
Disease Susceptibility
35 Citations (Scopus)

Genome-Wide Scan for a Healthy Aging Phenotype Provides Support for a Locus Near D4S1564 Promoting Healthy Aging

Reed, T., Dick, D. M., Uniacke, S. K., Foroud, T. & Nichols, W. C., Mar 2004, In : Journals of Gerontology - Series A Biological Sciences and Medical Sciences. 59, 3, p. 227-232 6 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 4
Genome
Phenotype
Dizygotic Twins
Prostatic Neoplasms
17 Citations (Scopus)

Glutathione S-transferase 8-8 expression is lower in alcohol-preferring than in alcohol-nonpreferring rats

Liang, T., Habegger, K., Spence, J. P., Foroud, T., Ellison, J. A., Lumeng, L., Li, T. K. & Carr, L. G., Nov 2004, In : Alcoholism: Clinical and Experimental Research. 28, 11, p. 1622-1628 7 p.

Research output: Contribution to journalArticle

Glutathione Transferase
Rats
Alcohols
Third Ventricle
Brain
108 Citations (Scopus)

Linkage and linkage disequilibrium of evoked EEG oscillations with CHRM2 receptor gene polymorphisms: Implications for human brain dynamics and cognition

Jones, K. A., Porjesz, B., Almasy, L., Bierut, L., Goate, A., Wang, J. C., Dick, D. M., Hinrichs, A., Kwon, J., Rice, J. P., Rohrbaugh, J., Stock, H., Wu, W., Bauer, L. O., Chorlian, D. B., Crowe, R. R., Edenberg, H., Foroud, T., Hesselbrock, V., Kuperman, S. & 7 others, Nurnberger, J., O'Connor, S., Schuckit, M. A., Stimus, A. T., Tischfield, J. A., Reich, T. & Begleiter, H., Jul 2004, In : International Journal of Psychophysiology. 53, 2, p. 75-90 16 p.

Research output: Contribution to journalArticle

Linkage Disequilibrium
Cognition
Single Nucleotide Polymorphism
Electroencephalography
P300 Event-Related Potentials
57 Citations (Scopus)

Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees

Schulze, T. G., Buervenich, S., Badner, J. A., Steele, C. J. M., Detera-Wadleigh, S. D., Dick, D., Foroud, T., Cox, N. J., MacKinnon, D. F., Potash, J. B., Berrettini, W. H., Byerley, W., Coryell, W., DePaulo, J. R., Gershon, E. S., Kelsoe, J. R., McInnis, M. G., Murphy, D. L., Reich, T., Scheftner, W. & 2 others, Nurnberger, J. & McMahon, F. J., Jul 1 2004, In : Biological Psychiatry. 56, 1, p. 18-23 6 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Pedigree
Mood Disorders
Bipolar Disorder
Chromosomes
61 Citations (Scopus)

Oculomotor control in asymptomatic and recently diagnosed individuals with the genetic marker for Huntington's disease

Blekher, T. M., Yee, R. D., Kirkwood, S. C., Hake, A., Stout, J. C., Weaver, M. R. & Foroud, T., Oct 2004, In : Vision Research. 44, 23, p. 2729-2736 8 p.

Research output: Contribution to journalArticle

Saccades
Huntington Disease
Genetic Markers
Optokinetic Nystagmus
Genes
51 Citations (Scopus)

Peak bone mineral density at the hip is linked to chromosomes 14q and 15q

Peacock, M., Koller, D. L., Hui, S., Johnston, C. C., Foroud, T. & Econs, M., Jun 2004, In : Osteoporosis International. 15, 6, p. 489-496 8 p.

Research output: Contribution to journalArticle

Bone Density
Hip
Chromosomes
Siblings
African Americans
29 Citations (Scopus)

Root resorption associated with orthodontic force in IL-1B knockout mouse

Al-Qawasmi, R. A., Hartsfield, J. K., Everett, E. T., Weaver, M. R., Foroud, T. & Roberts, W. E., Dec 2004, In : Journal of Musculoskeletal Neuronal Interactions. 4, 4, p. 383-385 3 p.

Research output: Contribution to journalArticle

Orthodontic Appliances
Root Resorption
Tooth Root
Animal Disease Models
Mechanical Stress
48 Citations (Scopus)

The search for genetic risk factors associated with suicidal behavior

Hesselbrock, V., Dick, D., Hesselbrock, M., Foroud, T., Schuckit, M., Edenberg, H., Bucholz, K., Kramer, J., Reich, T., Goate, A., Bierut, L., Rice, J. P. & Nurnberger, J., May 2004, In : Alcoholism: Clinical and Experimental Research. 28, 5 SUPPL.

Research output: Contribution to journalArticle

Chromosomes
Suicide
Alcohols
Lod Score
Alcoholism
475 Citations (Scopus)

Variations in GABRA2, Encoding the α2 Subunit of the GABA A Receptor, Are Associated with Alcohol Dependence and with Brain Oscillations

Edenberg, H., Dick, D. M., Xuei, X., Tian, H., Almasy, L., Bauer, L. O., Crowe, R. R., Goate, A., Hesselbrock, V., Jones, K., Kwon, J., Li, T. K., Nurnberger, J., O'Connor, S., Reich, T., Rice, J., Schuckit, M. A., Porjesz, B., Foroud, T. & Begleiter, H., Apr 2004, In : American Journal of Human Genetics. 74, 4, p. 705-714 10 p.

Research output: Contribution to journalArticle

GABA-A Receptors
Alcoholism
Single Nucleotide Polymorphism
Brain
Genes
2003
19 Citations (Scopus)

Analyses of Quantitative Trait Loci Contributing to Alcohol Preference in HAD1/LAD1 and HAD2/LAD2 Rats

Carr, L. G., Habegger, K., Spence, J., Ritchotte, A., Liu, L., Lumeng, L., Li, T. K. & Foroud, T., Nov 2003, In : Alcoholism: Clinical and Experimental Research. 27, 11, p. 1710-1717 8 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Rats
Alcohols
Animals
Chromosomes
91 Citations (Scopus)

Association of GABAA receptors and alcohol dependence and the effects of genetic imprinting

Song, J., Koller, D. L., Foroud, T., Carr, K., Zhao, J., Rice, J., Nurnberger, J., Begleiter, H., Porjesz, B., Smith, T. L., Schuckit, M. A. & Edenberg, H., Feb 15 2003, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 117 B, 1, p. 39-45 7 p.

Research output: Contribution to journalArticle

Genomic Imprinting
GABA-A Receptors
Alcoholism
Chromosomes, Human, Pair 15
Alleles
178 Citations (Scopus)

Candidate genes for alcohol dependence: A review of genetic evidence from human studies

Dick, D. M. & Foroud, T., May 1 2003, In : Alcoholism: Clinical and Experimental Research. 27, 5, p. 868-879 12 p.

Research output: Contribution to journalArticle

Nerve Tissue Proteins
Dopamine Plasma Membrane Transport Proteins
GABA Receptors
Membrane Transport Proteins
Alcohol Dehydrogenase
69 Citations (Scopus)

Chloride channel 7 (CLCN7) gene mutations and autosomal dominant osteopetrosis, type II

Waguespack, S. G., Koller, D. L., White, K., Fishburn, T., Carn, G., Buckwalter, K., Johnson, M., Kocisko, M., Evans, W. E., Foroud, T. & Econs, M., Aug 2003, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 18, 8, p. 1513-1518 6 p.

Research output: Contribution to journalArticle

Osteopetrosis
Chloride Channels
Mutation
Genes
Penetrance
15 Citations (Scopus)

Confirmation of alcohol preference quantitative trait loci in the replicate high alcohol drinking and low alcohol drinking rat lines

Foroud, T., Ritchotte, A., Spence, J., Liu, L., Lumeng, L., Li, T. K. & Carr, L. G., Sep 2003, In : Psychiatric Genetics. 13, 3, p. 155-161 7 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Alcohol Drinking
Alcohols
Chromosomes, Human, Pair 10
Chromosomes, Human, Pair 5
63 Citations (Scopus)

Genetic Effects for Femoral Biomechanics, Structure, and Density in C57BL/6J and C3H/HeJ Inbred Mouse Strains

Koller, D. L., Schriefer, J., Sun, Q., Shultz, K. L., Donahue, L. R., Rosen, C. J., Foroud, T., Beamer, W. G. & Turner, C. H., Oct 2003, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 18, 10, p. 1758-1765 8 p.

Research output: Contribution to journalArticle

Inbred Strains Mice
Quantitative Trait Loci
Thigh
Biomechanical Phenomena
Phenotype
127 Citations (Scopus)

Genetic predisposition to external apical root resorption

Al-Qawasmi, R. A., Hartsfield, J. K., Everett, E. T., Flury, L., Liu, L., Foroud, T., Macri, J. V. & Roberts, W. E., Mar 2003, In : American Journal of Orthodontics and Dentofacial Orthopedics. 123, 3, p. 242-252 11 p.

Research output: Contribution to journalArticle

Root Resorption
Genetic Predisposition to Disease
Interleukin-1
Incisor
Alleles
91 Citations (Scopus)

Genetic predisposition to external apical root resorption in orthodontic patients: Linkage of chromosome-18 marker

Al-Qawasmi, R. A., Hartsfield, J. K., Everett, E. T., Flury, L., Liu, L., Foroud, T., Macri, J. V. & Roberts, W. E., May 2003, In : Journal of Dental Research. 82, 5, p. 356-360 5 p.

Research output: Contribution to journalArticle

Root Resorption
Chromosomes, Human, Pair 18
Genetic Predisposition to Disease
Orthodontics
Genetic Markers
338 Citations (Scopus)

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

Segurado, R., Detera-Wadleigh, S. D., Levinson, D. F., Lewis, C. M., Gill, M., Nurnberger, J., Craddock, N., DePaulo, J. R., Baron, M., Gershon, E. S., Ekholm, J., Cichon, S., Turecki, G., Claes, S., Kelsoe, J. R., Schofield, P. R., Badenhop, R. F., Morissette, J., Coon, H., Blackwood, D. & 58 others, Mclnnes, L. A., Foroud, T., Edenberg, H., Reich, T., Rice, J. P., Goate, A., McInnis, M. G., McMahon, F. J., Badner, J. A., Goldin, L. R., Bennett, P., Willour, V. L., Zandi, P. P., Liu, J., Gilliam, C., Juo, S. H., Berrettini, W. H., Yoshikawa, T., Peltonen, L., Lönnqvist, J., Nöthen, M. M., Schumacher, J., Windemuth, C., Rietschel, M., Propping, P., Maier, W., Alda, M., Grof, P., Rouleau, G. A., Del-Favero, J., Van Broeckhoven, C., Mendlewicz, J., Adolfsson, R., Spence, M. A., Luebbert, H., Adams, L. J., Donald, J. A., Mitchell, P. B., Barden, N., Shink, E., Byerley, W., Muir, W., Visscher, P. M., Macgregor, S., Gurling, H., Kalsi, G., McQuillin, A., Escamilla, M. A., Reus, V. I., Leon, P., Freimer, N. B., Ewald, H., Kruse, T. A., Mors, O., Radhakrishna, U., Blouin, J. L., Antonarakis, S. E. & Akarsu, N., Jul 1 2003, In : American Journal of Human Genetics. 73, 1, p. 49-62 14 p.

Research output: Contribution to journalArticle

Bipolar Disorder
Meta-Analysis
Schizophrenia
Chromosomes
Genome
36 Citations (Scopus)

Genome scan of a second wave of NIMH genetics initiative bipolar pedigrees: Chromosomes 2, 11, 13, 14, and X

Zandi, P. P., Willour, V. L., Huo, Y., Chellis, J., Potash, J. B., MacKinnon, D. F., Simpson, S. G., McMahon, F. J., Gershon, E., Reich, T., Foroud, T., Nurnberger, J., DePaulo, J. R. & McInnis, M. G., May 15 2003, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 119 B, 1, p. 69-76 8 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 2
Pedigree
Bipolar Disorder
25 Citations (Scopus)

Genome scan of the fifty-six bipolar pedigrees from the NIMH genetics initiative replication sample: Chromosomes 4, 7, 9, 18, 19, 20, and 21

Willour, V. L., Zandi, P. P., Huo, Y., Diggs, T. L., Chellis, J. L., MacKinnon, D. F., Simpson, S. G., McMahon, F. J., Potash, J. B., Gershon, E. S., Reich, T., Foroud, T., Nurnberger, J., DePaulo, J. R. & McInnis, M. G., Aug 15 2003, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 121 B, 1, p. 21-27 7 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 7
Pedigree
Genome
172 Citations (Scopus)

Genomewide linkage analyses of bipolar disorder: A new sample of 250 pedigrees from the national institute of mental health genetics initiative

Dick, D. M., Foroud, T., Flury, L., Bowman, E. S., Miller, M. J., Rau, N. L., Moe, P. R., Samavedy, N., El-Mallakh, R., Manji, H., Glitz, D. A., Meyer, E. T., Smiley, C., Hahn, R., Widmark, C., McKinney, R., Sutton, L., Ballas, C., Grice, D., Berrettini, W. & 12 others, Byerley, W., Coryell, W., DePaulo, R., MacKinnon, D. F., Gershon, E. S., Kelsoe, J. R., McMahon, F. J., McInnis, M., Murphy, D. L., Reich, T., Scheftner, W. & Nurnberger, J., Jul 1 2003, In : American Journal of Human Genetics. 73, 1, p. 107-114 8 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Pedigree
Bipolar Disorder
Chromosomes
Chromosomes, Human, Pair 10
111 Citations (Scopus)

Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families

Pankratz, N., Nichols, W. C., Uniacke, S. K., Halter, C., Murrell, J., Rudolph, A., Shults, C. W., Conneally, P. M., Foroud, T., Truong, D., Pathak, M., Tran, A., Rodnitzky, R., Dobson, J., Koller, W., Weiner, W., Lyons, K., Kurlan, R., Berry, D., Bertoni, J. & 71 others, Peterson, C., Martin, W., Wieler, M., Tuite, P., Schacherer, R., Marder, K., Harris, J., Jankovic, J., Hunter, C., Lang, A., Kleimer-Fisman, G., Nieves, A., So, J., Factor, S., Evans, S., Manyam, B., Wulbrecht, B., Walker, F., Hunt, V., Gordon, M. F., Hamman, J., Kang, U. J., Young, J., Blindauer, K., Petit, J., Rao, J., Cook, M., Stacy, M., Williamson, K., Pullman, R. S., Boyar, K., Leehey, M., Derian, T., Gordon, P., Werner, J., Racette, B., Good, L., Simon, D., Scollins, L., Schwieterman, D., Dewey, R., Meacham, M., Sutton, J., Hutchinson, B., Jog, M., Horn, C., Sethi, K., Carpenter, J., Atchison, P., Rolli, S., Sudarsky, L., Corwin, C., Velickovic, M., Phipps, S., Simuni, T., Kaczmarek, A., Hermanowicz, N., Niswonger, S., Feigin, A., Shannon, B., Calabrese, V., Roberge, P., Homes, H., Shulman, L., Dustin, K., Ajax, T., Mannetter, J., Podskalny, G. D., Giffin, L., Uitti, R. & Turk, M. F., Oct 15 2003, In : Human Molecular Genetics. 12, 20, p. 2599-2608 10 p.

Research output: Contribution to journalArticle

Parkinson Disease
Genome
Genes
Chromosomes, Human, Pair 2
Siblings
67 Citations (Scopus)

Genome-wide scan and conditional analysis in bipolar disorder: Evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees

McInnis, M. G., Dick, D. M., Willour, V. L., Avramopoulos, D., MacKinnon, D. F., Simpson, S. G., Potash, J. B., Edenberg, H., Bowman, E. S., McMahon, F. J., Smiley, C., Chellis, J. L., Huo, Y., Diggs, T., Meyer, E. T., Miller, M., Matteini, A. T., Rau, N. L., DePaulo, J. R., Gershon, E. S. & 8 others, Badner, J. A., Rice, J. P., Goate, A. M., Detera-Wadleigh, S. D., Nurnberger, J., Reich, T., Zandi, P. P. & Foroud, T., Dec 1 2003, In : Biological Psychiatry. 54, 11, p. 1265-1273 9 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Pedigree
Bipolar Disorder
Genome
Genes
173 Citations (Scopus)

Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease

Foroud, T., Uniacke, S. K., Liu, L., Pankratz, N., Rudolph, A., Halter, C., Shults, C., Marder, K., Conneally, P. M., Nichols, W. C., Golbe, L., Koller, W., Lyons, K., Marshall, F., Oakes, D., Shinaman, A., Siemers, E., Wojcieszek, J., Belden, J., Carter, J. & 79 others, Camicioli, R., Andrews, P., Fernandez, M., Hubble, J., Reider, C., Rajput, A., Rajput, A., Shirley, T., Panisset, M., Hall, J., Mendis, T., Grimes, D. A., Gray, P., Serrano Ramos, C., Roque, S., Reich, S., Dunlop, B., Hauser, R., Sanchez-Ramos, J., Zesiewicz, T., Delgado, H., Friedman, J., Fernandez, H., Lannon, M., Seeberger, L., O'Brien, C., Judd, D., Elmer, L., Davis, K., Fontaine, D., Pfeiffer, R., Pfeiffer, B., Aminoff, M., DiMinno, M., Truong, D., Pathak, M., Tran, A., Rodnitzky, R., Dobson, J., Pahwa, R., Thomas, S., Jennings, D., Marek, K., Mendick, S., Harris, J., Weiner, W., Kurlan, R., Berry, D., Lewitt, P., DeAngelis, M., Tuite, P., Schacherer, R., Martin, W., Wieler, M., Manyam, B., Simpson, P., Bertoni, J., Peterson, C., Gordon, M. F., Hamann, J., Jankovic, J., Hunter, C., Factor, S., Evans, S., Nieves, A., So, J., Stacy, M., Williamson, K., Walker, F., Hunt, V., Kang, U. J., Uy, S., Bindauer, K., Petit, J., Simon, D., Scollins, L., Pullman, R. S., Boyer, K. & Gordon, P., Mar 11 2003, In : Neurology. 60, 5, p. 796-801 6 p.

Research output: Contribution to journalArticle

Parkinson Disease
Mutation
Genes
Age of Onset
Alleles
4 Citations (Scopus)

Identification of genes for complex disease using longitudinal phenotypes.

Pankratz, N., Mukhopadhyay, N., Huang, S., Foroud, T. & Kirkwood, S. C., 2003, In : BMC Genetics. 4 Suppl 1, S58.

Research output: Contribution to journalArticle

Phenotype
Genes
Information Dissemination
Genome
Education
2 Citations (Scopus)

Interpretation of Genetic Linkage Findings (multiple letters)

Liu, Y., Xu, F., Recker, R. R., Deng, H. W., Koller, D. L., White, K., Liu, G., Hui, S., Conneally, P. M., Johnston, C. C., Econs, M., Foroud, T. & Peacock, M., Nov 2003, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 18, 11, p. 2077-2080 4 p.

Research output: Contribution to journalArticle

Lod Score
Genetic Linkage
Chromosome Mapping
Quantitative Trait Loci
Reproducibility of Results
32 Citations (Scopus)

Linkage mapping of Beta 2 EEG waves via non-parametric regression

Ghosh, S., Begleiter, H., Porjesz, B., Chorlian, D. B., Edenberg, H., Foroud, T., Goate, A. & Reich, T., Apr 1 2003, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 118 B, 1, p. 66-71 6 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 4
Chromosome Mapping
Chromosomes, Human, Pair 15
Electroencephalography
Chromosomes, Human, Pair 1
39 Citations (Scopus)

Linkage of Structure at the Proximal Femur to Chromosomes 3, 7, 8, and 19

Koller, D. L., White, K., Liu, G., Hui, S., Conneally, P. M., Johnston, C. C., Econs, M., Foroud, T. & Peacock, M., Jun 1 2003, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 18, 6, p. 1057-1065 9 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 3
Chromosomes, Human, Pair 7
Thigh
Femur
Chromosomes, Human, Pair 19
33 Citations (Scopus)

Prenatal alcohol exposure: Advancing knowledge through international collaborations

Riley, E. P., Guerri, C., Calhoun, F., Charness, M. E., Foroud, T., Li, T. K., Mattson, S. N., May, P. A. & Warren, K. R., Jan 1 2003, In : Alcoholism: Clinical and Experimental Research. 27, 1, p. 118-135 18 p.

Research output: Contribution to journalArticle

Fetal Alcohol Spectrum Disorders
Alcohols
Population
Chile
Russia
27 Citations (Scopus)

Reliability of reported age at onset of Parkinson's disease

Reider, C. R., Halter, C. A., Castelluccio, P. F., Oakes, D., Nichols, W. C., Foroud, T., Wolff, A., Dewey, R., Jones, M., Hermanowicz, N., Feigin, A., Shannon, B., Calabresse, V., Roberge, P., Sutton, J., Hutchinson, B., Ajax, T., Mannetter, J., Podakalny, G. D., Giffin, L. & 6 others, Suchowersky, O., Klimek, M. L., Uitti, R., Foster Turk, M., Shulman, L. & Dustin, K., Mar 1 2003, In : Movement Disorders. 18, 3, p. 275-279 5 p.

Research output: Contribution to journalArticle

Age of Onset
Parkinson Disease
Medical Records
History
Observation
121 Citations (Scopus)

Significant linkage of Parkinson disease to chromosome 2q36-37

Pankratz, N., Nichols, W. C., Uniacke, S. K., Halter, C., Rudolph, A., Shults, C., Conneally, P. M., Foroud, T., Golbe, L., Koller, W., Lyons, K., Marder, K., Marshall, F., Oakes, D., Shinaman, A., Siemers, E., Wojcieszek, J., Belden, J., Carter, J., Camicioli, R. & 79 others, Andrews, P., Fernandez, M., Hubble, J., Reider, C., Rajput, A., Rajput, A., Shirley, T., Panisset, M., Hall, J., Mendis, T., Grimes, D. A., Gray, P., Ramos, C. S., Roque, S., Reich, S., Dunlop, B., Hauser, R., Sanchez-Ramos, J., Zesiewicz, T., Delgado, H., Friedman, J., Fernandez, H., Lannon, M., Seeberger, L., O'Brien, C., Judd, D., Elmer, L., Davis, K., Fontaine, D., Pfeiffer, R., Pfeiffer, B., Aminoff, M., DiMinno, M., Truong, D., Pathak, M., Tran, A., Rodnitzky, R., Dobson, J., Pahwa, R., Thomas, S., Jennings, D., Marek, K., Mendick, S., Harris, J., Weiner, W., Kurlan, R., Berry, D., Lewitt, P., DeAngelis, M., Tuite, P., Schacherer, R., Martin, W., Wieler, M., Manyam, B., Simpson, P., Bertoni, J., Peterson, C., Gordon, M. F., Hamann, J., Jankovic, J., Hunter, C., Factor, S., Evans, S., Nieves, A., So, J., Stacy, M., Williamson, K., Walker, F., Hunt, V., Kang, U. J., Uy, S., Blindauer, K., Petit, J., Simon, D., Scollins, L., Pullman, R. S., Boyar, K., Gordon, P. & Werner, J., Apr 1 2003, In : American Journal of Human Genetics. 72, 4, p. 1053-1057 5 p.

Research output: Contribution to journalArticle

Parkinson Disease
Chromosomes
Pedigree
Disease Susceptibility
Neurodegenerative Diseases