Year |
Title |
Altmetric |
2021
|
Cognitive Processing Speed Is Strongly Related to Driving Skills, Financial Abilities, and Other Instrumental Activities of Daily Living in Persons with Mild Cognitive Impairment and Mild Dementia
2021
|
|
2021
|
Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis.
JAMA Neurology.
78:102-113.
2021
|
|
2020
|
Genome-wide epigenetic analyses in Japanese immigrant plantation workers with Parkinson's disease and exposure to organochlorines reveal possible involvement of glial genes and pathways involved in neurotoxicity.
BMC Neuroscience.
21.
2020
|
|
2016
|
Association of DNA methylation differences with schizophrenia in an epigenome-wide association study.
JAMA Psychiatry.
73:506-514.
2016
|
|
2016
|
Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk.
Alzheimer's and Dementia.
12:233-243.
2016
|
|
2015
|
Association of long runs of homozygosity with Alzheimer disease among African American individuals.
JAMA Neurology.
72:1313-1323.
2015
|
|
2013
|
XSpatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network.
Cell.
154.
2013
|
|
2013
|
Persistent infection with neurotropic herpes viruses and cognitive impairment.
Psychological Medicine.
43:1023-1031.
2013
|
|
2013
|
Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein e ε4, and the risk of late-onset Alzheimer disease in African Americans.
Journal of the American Medical Association.
309:1483-1492.
2013
|
|
2013
|
Principal components of heritability from neurocognitive domains differ between families with schizophrenia and control subjects.
Schizophrenia Bulletin.
39:464-471.
2013
|
|
2012
|
Evaluation of HLA polymorphisms in relation to schizophrenia risk and infectious exposure.
Schizophrenia Bulletin.
38:1149-1154.
2012
|
|
2012
|
Heritability of functioning in families with schizophrenia in relation to neurocognition.
Schizophrenia Research.
139:105-109.
2012
|
|
2012
|
Association between family risk of stroke and myocardial infarction with prevalent risk factors and coexisting diseases.
Stroke.
43:974-979.
2012
|
|
2011
|
Comparison of measures of marker informativeness for ancestry and admixture mapping.
BMC Genomics.
12.
2011
|
|
2011
|
Vascular risk factors and cognitive impairment in a stroke-free cohort.
Neurology.
77:1729-1736.
2011
|
|
2011
|
Incident cognitive impairment is elevated in the stroke belt: The REGARDS Study.
Annals of Neurology.
70:229-236.
2011
|
|
2011
|
A comprehensive genetic association study of Alzheimer disease in African Americans.
JAMA Neurology.
68:1569-1579.
2011
|
|
2010
|
Project Among African-Americans to Explore Risks for schizophrenia (paartners): Evidence for impairment and heritability of Neurocognitive functioning in families of schizophrenia patients.
American Journal of Psychiatry.
167:459-472.
2010
|
|
2009
|
Genetic risk factors for type 2 diabetes with pharmacologic intervention in African-American patients with schizophrenia or schizoaffective disorder.
Schizophrenia Research.
114:50-56.
2009
|
|
2009
|
Association of higher diastolic blood pressure levels with cognitive impairment.
Neurology.
73:589-595.
2009
|
|
2009
|
Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.
150:560-569.
2009
|
|
2009
|
Database mining for selection of SNP markers useful in admixture mapping.
BioData Mining.
2.
2009
|
|
2009
|
Linkage analysis of schizophrenia in African-American families.
Schizophrenia Research.
109:70-79.
2009
|
|
2008
|
A genomic scan for age at onset of Alzheimer's disease in 437 families from the NIMH genetic initiative.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.
147:784-792.
2008
|
|
2008
|
Kidney Function and Cognitive Impairment in US Adults: The Reasons for Geographic and Racial Differences in Stroke (REGARDS) Study.
American Journal of Kidney Diseases.
52:227-234.
2008
|
|
2008
|
Regional differences in diabetes as a possible contributor to the geographic disparity in stroke mortality: The REasons for geographic and racial differences in stroke study.
Stroke.
39:1675-1680.
2008
|
|
2008
|
Genetic association of neurotrophic tyrosine kinase receptor type 2 (NTRK2) with Alzheimer's disease.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.
147:363-369.
2008
|
|
2008
|
Hemoglobin binding to Aβ and HBG2 SNP association suggest a role in Alzheimer's disease.
Neurobiology of Aging.
29:185-193.
2008
|
|
2008
|
Candidate gene discovery procedure after follow-up confirmatory analyses of candidate regions of interests for Alzheimer's disease in the NIMH sibling dataset.
Disease Markers.
24:293-309.
2008
|
|
2007
|
Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease.
Human Molecular Genetics.
16:2703-2712.
2007
|
|
2007
|
Effects of chronic stress and interleukin-10 gene polymorphisms on antibody response to tetanus vaccine in family caregivers of patients with Alzheimer's disease.
Psychosomatic Medicine.
69:551-559.
2007
|
|
2007
|
Cognitive status, stroke symptom reports, and modifiable risk factors among individuals with no diagnosis of stroke or transient ischemic attack in the REasons for Geographic and Racial Differences in Stroke (REGARDS) study.
Stroke.
38:1143-1147.
2007
|
|
2007
|
Follow-up mapping supports the evidence for linkage in the candidate region at 9q22 in the NIMH Alzheimer's disease genetics initiative cohort.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.
144:220-227.
2007
|
|
2007
|
Knowledge of and attitudes about Alzheimer disease genetics: Report of a pilot survey and two focus groups.
Public Health Genomics.
10:97-102.
2007
|
|
2007
|
Erratum to "Project among African-Americans to explore risks for schizophrenia (PAARTNERS): Recruitment and assessment methods" [Schizophrenia Research 87 (1-3) (2006) 32-44] (DOI:10.1016/j.schres.2006.06.027).
Schizophrenia Research.
90:369.
2007
|
|
2007
|
A polymorphism in SOD2 is associated with development of Alzheimer's disease.
Genes, Brain and Behavior.
6:770-776.
2007
|
|
2006
|
Further evidence of a maternal parent-of-origin effect on chromosome 10 in late-onset Alzheimer's disease.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.
141:537-540.
2006
|
|
2006
|
Genetic association between endothelial nitric oxide synthase and Alzheimer disease
2006
|
|
2006
|
Increased frequency of HLA-B44 in recurrent sinopulmonary infections (RESPI).
Clinical Immunology.
119:346-350.
2006
|
|
2006
|
African-American community attitudes and perceptions toward schizophrenia and medical research: An exploratory study.
Journal of the National Medical Association.
98:18-27.
2006
|
|
2006
|
Polymorphisms in the PON gene cluster are associated with Alzheimer disease.
Human Molecular Genetics.
15:77-85.
2006
|
|
2006
|
Project among African-Americans to explore risks for schizophrenia (PAARTNERS): Recruitment and assessment methods.
Schizophrenia Research.
87:32-44.
2006
|
|
2005
|
COGA phenotypes and linkages on chromosome 2.
BMC Genomic Data.
6.
2005
|
|
2005
|
Association studies of transforming growth factor-β1 and Alzheimer's disease.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.
139 B:38-41.
2005
|
|
2005
|
Neuregulin-1 polymorphism in late onset Alzheimer's disease families with psychoses.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.
139 B:28-32.
2005
|
|
2005
|
The reasons for geographic and racial differences in stroke study: Objectives and design.
Neuroepidemiology.
25:135-143.
2005
|
|
2005
|
Total blood lymphocyte counts in hemochromatosis probands with HFE C282Y homozygosity: Relationship to severity of iron overload and HLA-A and -B alleles and haplotypes.
BMC Hematology.
5.
2005
|
|
2005
|
HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: Frequency disparity in men and women and lack of association with severity of iron overload.
Blood Cells, Molecules and Diseases.
34:38-47.
2005
|
|
2004
|
Is cumulative frequency of mitochondrial DNA variants a biomarker for colorectal tumor progression?.
Molecular Cancer.
3.
2004
|
|
2004
|
Ancestry reported by white adults with cutaneous melanoma and control subjects in central Alabama.
BMC Cancer.
4.
2004
|
|
2004
|
Genetics and cardiovascular disease.
2004
|
|
2003
|
Genetic association of Alzheimer's disease with multiple polymorphisms in alpha-2-macroglobulin.
Human Molecular Genetics.
12:2765-2776.
2003
|
|
2003
|
"Are We There Yet?": Deciding When One Has Demonstrated Specific Genetic Causation in Complex Diseases and Quantitative Traits.
American Journal of Human Genetics.
73:711-719.
2003
|
|
2003
|
No association between marker D10S1423 and Alzheimer's disease.
Molecular Psychiatry.
8:571-573.
2003
|
|
2003
|
Depression as a risk factor for Alzheimer disease: The MIRAGE Study.
JAMA Neurology.
60:753-759.
2003
|
|
2003
|
Erratum to "The role of TNF and its receptors in Alzheimer's disease": [Neurobiology of Aging 22 (2001) 873-883].
Neurobiology of Aging.
24:519-520.
2003
|
|
2003
|
Results of a high-resolution genome screen of 437 Alzheimer's Disease families.
Human Molecular Genetics.
12:23-32.
2003
|
|
2002
|
Risk of dementia among white and African American relatives of patients with Alzheimer disease.
Journal of the American Medical Association.
287:329-336.
2002
|
|
2002
|
Association between apolipoprotein E genotype and Alzheimer disease in African American subjects.
JAMA Neurology.
59:594-600.
2002
|
|
2001
|
The role of TNF and its receptors in Alzheimer's disease.
Neurobiology of Aging.
22:873-883.
2001
|
|
2001
|
Investigation of association of 13 polymorphisms in eight genes in southeastern African American Alzheimer disease patients as compared to age-matched controls.
American Journal of Medical Genetics Part A.
105:332-342.
2001
|
|
2001
|
No evidence for genetic association or linkage of the cathepsin D (CTSD) exon 2 polymorphism and Alzheimer disease.
Annals of Neurology.
49:114-116.
2001
|
|
2001
|
Prevalence of polycystic ovary syndrome (PCOS) in first-degree relatives of patients with PCOS.
Fertility and Sterility.
75:53-58.
2001
|
|
2001
|
HFE mutations in African-American women with non-insulin-dependent diabetes mellitus
2001
|
|
2001
|
Prevalence and risk factors of microalbuminuria in a cohort of African-American women with gestational diabetes.
Diabetes reviews (Alexandria, Va.).
24:1764-1769.
2001
|
|
2000
|
Evidence for genetic linkage Alzheimer's disease to chromosome 10q.
Science.
290:2302-2303.
2000
|
|
2000
|
Association of a haplotype for tumor necrosis factor in siblings with late-onset Alzheimer disease: The NIMH Alzheimer disease genetics initiative.
American Journal of Medical Genetics Part A.
96:823-830.
2000
|
|
2000
|
Genomic structure, expression pattern, and chromosomal localization of the human calsenilin gene: No association between an exonic polymorphism and Alzheimer's disease.
Neuroscience Letters.
294:135-138.
2000
|
|
2000
|
Head injury and the risk of AD in the MIRAGE study.
Neurology.
54:1316-1323.
2000
|
|
2000
|
High prevalence of complement component C6 deficiency among African- Americans in the South-eastern USA.
Clinical and Experimental Immunology.
119:305-310.
2000
|
|
1999
|
Associations of MHC genes with levels of caries-inducing organisms and caries severity in African-American women.
Human Immunology.
60:984-989.
1999
|
|
1998
|
Polymorphic tetranucleotide repeat site within intron 7 of the β-amyloid precursor protein gene and its lack of association with Alzheimer's disease.
Human Genetics.
103:86-89.
1998
|
|
1998
|
Alpha-2 macroglobulin is genetically associated with Alzheimer disease.
Nature Genetics.
19:357-360.
1998
|
|
1998
|
Gene polymorphisms for PAI-1 are associated with the angiographic Extent of coronary artery disease.
Journal of Thrombosis and Thrombolysis.
5:143-150.
1998
|
|
1998
|
Susceptibility locus for IgA deficiency and common variable immunodeficiency in the HLA-DR3, -B8, -A1 haplotypes.
Molecular Medicine.
4:72-86.
1998
|
|
1997
|
Instability of the FMR2 trinucleotide repeat region associated with expanded FMR1 alleles.
American Journal of Medical Genetics Part A.
73:447-455.
1997
|
|
1997
|
Rapid determination of clonality by detection of two closely-linked X chromosome exonic polymorphisms using allele-specific PCR.
Journal of Clinical Investigation.
99:1984-1990.
1997
|
|
1997
|
ApoE-4 and age at onset of Alzheimer's disease: The NIMH genetics initiative.
Neurology.
48:139-147.
1997
|
|
1997
|
Development and validation of a structured telephone interview for dementia assessment (STIDA): The NIMH genetics initiative.
Journal of Geriatric Psychiatry and Neurology.
10:161-167.
1997
|
|
1996
|
Genetic epidemiologic methods to screen for matrilineal inheritance in mitochondrial disorders.
Genetic Epidemiology.
13:605-614.
1996
|
|
1995
|
SSCP analysis and sequencing of the human prion protein gene (PRNP) detects two different 24 bp deletions in an atypical Alzheimer's disease family.
American Journal of Medical Genetics Part A.
60:12-18.
1995
|
|
1994
|
Genes within the major histocompatibility complex predict NIDDM in African-American women in Alabama.
Diabetes reviews (Alexandria, Va.).
17:1491-1494.
1994
|
|
1994
|
Glucokinase gene in gestational diabetes mellitus: population association study and molecular scanning.
Diabetologia.
37:104-110.
1994
|
|
1994
|
HLA in ankylosing spondylitis: Is HLA-B27 the only MHC gene involved in disease pathogenesis?.
Seminars in Arthritis and Rheumatism.
23:295-309.
1994
|
|
1994
|
Plasma homocyst(e)ine, folate, and vitamin B-12 concentrations and risk for early-onset coronary artery disease.
American Journal of Clinical Nutrition.
59:940-948.
1994
|
|
1993
|
Association of HLA phenotypes with hypertension in African Americans and Caucasoid Americans with type II diabetes, a population at risk for renal disease.
Transplantation Proceedings.
25:2400-2403.
1993
|
|
1993
|
Comparison of HLA phenotypes among African Americans from Alabama, Maryland, and North Carolina.
Transplantation Proceedings.
25:2404-2407.
1993
|
|
1992
|
Major histocompatibility complex class III genes and susceptibility to immunoglobulin a deficiency and common variable immunodeficiency.
Journal of Clinical Investigation.
89:1914-1922.
1992
|
|
1992
|
Sexual differences in lipoprotein composition in a family with dyslipidemic hypertension with premature atheroschlerosis: Deficiency of high-density lipoprotein-L and high-density lipoprotein-M "apolipoprotein-I alone" particle
1992
|
|
1991
|
Autoantibodies in Black Women with Class A1 or Class GB Diabetes Mellitus.
American Journal of Perinatology.
8:103-105.
1991
|
|
1991
|
Gestational diabetes mellitus among African‐American women
1991
|
|
1991
|
Histocompatibility Antigen Subtypes in Black Women with Class A1 or Class GB Diabetes Mellitus.
American Journal of Perinatology.
8:106-109.
1991
|
|
1991
|
The relationship between maternal serum zinc levels during pregnancy and birthweight.
Early Human Development.
25:75-85.
1991
|
|
1990
|
A positive association between maternal serum zinc concentration and birth weight.
American Journal of Clinical Nutrition.
51:678-684.
1990
|
|
1990
|
Risk factors for gestational diabetes in black population.
Diabetes reviews (Alexandria, Va.).
13:1196-1201.
1990
|
|
1990
|
The effect of genetic risk information and health risk assessment on compliance with preventive behaviors.
American Journal of Health Education.
21:26-33.
1990
|
|
1989
|
The effect of risk assessment in conjunction with health promotion education on compliance with preventive behaviors..
Journal of Allied Health.
18:271-280.
1989
|
|
1988
|
Allelic Variants for Complement Factors C3, C4, and B in Acute Necrotizing Ulcerative Gingivitis
1988
|
|
1988
|
Association of HLA-linked factor B with gestational diabetes mellitus in black women.
American Journal of Obstetrics and Gynecology.
159:805-806.
1988
|
|
1987
|
Enhanced in vitro IgM rheumatoid factor synthesis in seropositive rheumatoid arthritis families
1987
|
|
1987
|
Risk factor surveys of the adult populations of the state of Alabama and Jefferson County..
The Alabama journal of medical sciences.
24:143-149.
1987
|
|
1986
|
Host Factors in Juvenile Periodontitis
1986
|
|
1985
|
Familial studies in human brucellosis.
HLA.
26:77-79.
1985
|
|
1985
|
Genetic predisposition to acute lymphocytic leukemia in American blacks. A pediatric oncology group study.
Cancer.
55:2880-2882.
1985
|
|
1984
|
The complement component C4 in black Americans with Type 1 (insulin-dependent) diabetes mellitus.
Diabetologia.
26:166-168.
1984
|
|
1984
|
Association of factor B with ischemic heart disease (IHD)..
Progress in clinical and biological research.
147:479-480.
1984
|
|
1984
|
Search for biological/genetic markers in a long-term epidemiological and morbid risk study of affective disorders.
Journal of Psychiatric Research.
18:425-445.
1984
|
|
1984
|
Segregation and linkage analyses of von Hippel Lindau disease among 220 descendants from one kindred.
American Journal of Human Genetics.
36:131-142.
1984
|
|
1983
|
Genetic epidemiology of breast cancer and associated cancers in high-risk families. I. Segregation analysis
1983
|
|
1983
|
Genetic epidemiology of breast cancer and associated cancers in high-risk families. II. Linkage analysis
1983
|
|
1983
|
Age at onset of insulin-dependent diabetes mellitus associated with BfF1.
Immunogenetics.
17:437-440.
1983
|
|
1983
|
Genetic analysis of multiply-affected families of insulin-dependent diabetes mellitus (Iddm) probands
1983
|
|
1983
|
PHENOTYPES OF THE FOURTH COMPLEMENT COMPONENT (C4) IN BLACK AMERICANS FROM THE SOUTHEASTERN UNITED STATES.
International Journal of Immunogenetics.
10:199-204.
1983
|
|
1983
|
Population genetic analyses of insulin dependent diabetes mellitus using HLA allele frequencies
1983
|
|
1982
|
Properdin factor B in black Type 1 (insulin-dependent) diabetic patients.
Diabetologia.
22:483-485.
1982
|
|
1982
|
Associations of properdin factor B with melanoma.
Cancer Genetics.
5:247-251.
1982
|
|
1982
|
Evidence for genetic admixture as a determinant in the occurrence of insulin-dependent diabetes mellitus in U.S. blacks.
Diabetes.
31:532-537.
1982
|
|
1982
|
HLA-A, -B, and -DR associations in type I diabetes mellitus with onset after age forty.
Diabetes.
31:122-125.
1982
|
|
1982
|
Properdin factor B and acute lymphocytic leukemia (ALL).
Cancer.
50:2369-2371.
1982
|
|
1981
|
PROPERDIN FACTOR B POLYMORPHISM IN BLACK AMERICANS.
International Journal of Immunogenetics.
8:519-521.
1981
|
|
1981
|
Properdin factor B (Bf) phenotypes in blacks with insulin-dependent diabetes mellitus (IDDM)
1981
|
|
1980
|
Allele increasing susceptibility to human breast cancer may be linked to the glutamate-pyruvate transaminase locus.
Science.
208:407-408.
1980
|
|
1979
|
Clinical, genetic, and biostatistical progress in the cancer family syndrome..
Frontiers of gastrointestinal research.
4:142-150.
1979
|
|
1979
|
Possible linkage between α-haptoglobin (hp) and depression spectrum disease
1979
|
|
1978
|
Efficiency and robustness of pedigree segregation analysis.
American Journal of Human Genetics.
30:28-37.
1978
|
|
1978
|
Linkage relations among 25 autosomal blood, urine, and saliva markers in two large multigenerational pedigrees.
Cytogenetic and Genome Research.
22:633-639.
1978
|
|
1978
|
The malignancy of dementias.
Annals of Neurology.
3:559-561.
1978
|
|
1977
|
A Genetic Linkage Study in Support of the Concept of Depression Spectrum Disease.
Alcoholism: Clinical and Experimental Research.
1:119-123.
1977
|
|
1977
|
Association and linkage between genetic markers and morphological and behavioral attributes in dizygotic twins.
Biodemography and Social Biology.
24:62-68.
1977
|
|
1977
|
Blood markers and depressive disorders: An association study.
Comprehensive Psychiatry.
18:263-269.
1977
|
|
1977
|
Linkage relationships of Lp and Ag serum lipoproteins with 25 polymorphic markers.
Human Genetics.
37:291-297.
1977
|
|
1977
|
Possible linkage between Group‐Specific Component (Gc protein) and pure depressive disease.
Acta Psychiatrica Scandinavica.
55:111-115.
1977
|
|
1976
|
A linkage study of pure depressive disease: The use of the sib pair method.
Biological Psychiatry.
11:767-771.
1976
|
|
1976
|
Probable linkage between essential familial hypercholesterolemia and third complement component (C3) HUMAN GENE MAPPING.3..
Birth defects original article series.
12:294-297.
1976
|
|
1976
|
A linkage study of depression spectrum disease: The use of the sib pair method
1976
|
|
1976
|
Lack of association of genetic traits with alcoholism; C3, Ss and ABO systems.
Journal of Studies on Alcohol and Drugs.
37:1313-1315.
1976
|
|
1976
|
Probable linkage between essential familial hypercholesterolemia and third complement component (C3).
Cytogenetic and Genome Research.
16:294-297.
1976
|
|
1975
|
Familial hyper-alpha-lipoproteinemia: Studies in eighteen kindreds
1975
|
|
1975
|
Specificity of the clinical diagnosis of dementia.
Journal of the Neurological Sciences.
26:81-98.
1975
|
|