PBAT: tools for family-based association studies.

Longitudinal data analysis using generalized linear models

LIANG, K.-Y., & ZEGER, S. L. (1986) · Biometrika · doi:10.1093/biomet/73.1.13 · Cited by 18,550 · see citing works

A General Test of Association for Quantitative Traits in Nuclear Families

Abecasis, G. R., Cardon, L. R., & Cookson, W. O. C. (2000) · The American Journal of Human Genetics · doi:10.1086/302698 · Cited by 1,126 · see citing works

Implementing a unified approach to family-based tests of association

Laird, N. M., Horvath, S., & Xu, X. P. (2000) · Genetic Epidemiology · doi:10.1002/1098-2272(2000)19:1+ · Cited by 854 · see citing works

The family based association test method: strategies for studying general genotype–phenotype associations

Horvath, S., Xu, X. P., & Laird, N. M. (2001) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5200625 · Cited by 739 · see citing works

A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information.

Rabinowitz, D., & Laird, N. (2000) · Human Heredity · doi:10.1159/000022918 · Cited by 627 · see citing works

Family-Based Tests of Association in the Presence of Linkage

Lake, S. L., Blacker, D., & Laird, N. M. (2000) · The American Journal of Human Genetics · doi:10.1086/316895 · Cited by 267 · see citing works

A Discordant-Sibship Test for Disequilibrium and Linkage: No Need for Parental Data

Horvath, S., & Laird, N. M. (1998) · The American Journal of Human Genetics · doi:10.1086/302137 · Cited by 220 · see citing works

A multivariate family-based association test using generalized estimating equations: FBAT-GEE

Lange, C. (2003) · Biostatistics · doi:10.1093/biostatistics/4.2.195 · Cited by 198 · see citing works

Power and Design Considerations for a General Class of Family-Based Association Tests: Quantitative Traits

Lange, C., DeMeo, D. L., & Laird, N. M. (2002) · The American Journal of Human Genetics · doi:10.1086/344696 · Cited by 145 · see citing works

Power Calculations for a General Class of Family-Based Association Tests: Dichotomous Traits

Lange, C., & Laird, N. M. (2002) · The American Journal of Human Genetics · doi:10.1086/342406 · Cited by 119 · see citing works

Removing the Sampling Restrictions from Family-Based Tests of Association for a Quantitative-Trait Locus

Monks, S. A., & Kaplan, N. L. (2000) · The American Journal of Human Genetics · doi:10.1086/302745 · Cited by 116 · see citing works

On a general class of conditional tests for family‐based association studies in genetics: the asymptotic distribution, the conditional power, and optimality considerations

Lange, C., & Laird, N. M. (2002) · Genetic Epidemiology · doi:10.1002/gepi.209 · Cited by 108 · see citing works

IL10 gene polymorphisms are associated with asthma phenotypes in children

Lyon, H. N., Lange, C., Lake, S. L., et al. (2004) · Genetic Epidemiology · doi:10.1002/gepi.10298 · Cited by 99 · see citing works

Using the Noninformative Families in Family-Based Association Tests: A Powerful New Testing Strategy

Lange, C., DeMeo, D. L., Silverman, E. K., Weiss, S. T., & Laird, N. M. (2003) · The American Journal of Human Genetics · doi:10.1086/378591 · Cited by 82 · see citing works

Univariate and multivariate family‐based association analysis of the IL‐13 ARG130GLN polymorphism in the Childhood Asthma Management program

DeMeo, D. L., Lange, C., Silverman, E. K., et al. (2002) · Genetic Epidemiology · doi:10.1002/gepi.10182 · Cited by 69 · see citing works

A New Powerful Non-Parametric Two-Stage Approach for Testing Multiple Phenotypes in Family-Based Association Studies

Lange, C., Lyon, H. N., DeMeo, D. L., Raby, B. A., Silverman, E. K., & Weiss, S. T. (2003) · Human Heredity · doi:10.1159/000073728 · Cited by 54 · see citing works

Family‐based association tests for survival and times‐to‐onset analysis

Lange, C., Blacker, D., & Laird, N. M. (2004) · Statistics in Medicine · doi:10.1002/sim.1707 · Cited by 47 · see citing works

Generalized estimating equations: A hybrid approach for mean parameters in multivariate regression models

Lange, C., Whittaker, J. C., & MacGregor, A. J. (2002) · Statistical Modelling · doi:10.1191/1471082x02st031oa · Cited by 8 · see citing works

Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database

Bertram, L., McQueen, M. B., Mullin, K., Blacker, D., & Tanzi, R. E. (2007) · Nature Genetics · doi:10.1038/ng1934 · Cited by 1,857 · see citing works

Carnitine—metabolism and functions

Bremer, J. (1983) · Physiological Reviews · doi:10.1152/physrev.1983.63.4.1420 · Cited by 1,666 · see citing works

The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease

Rogaeva, E., Meng, Y., Lee, J. H., Gu, Y., Kawarai, T., Zou, F., Katayama, T., Baldwin, C. T., Cheng, R., Hasegawa, H., et al. (2007) · Nature Genetics · doi:10.1038/ng1943 · Cited by 1,167 · see citing works

Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database

Allen, N. C., Bagade, S., McQueen, M. B., Ioannidis, J. P. A., Kavvoura, F. K., Khoury, M. J., Tanzi, R. E., & Bertram, L. (2008) · Nature Genetics · doi:10.1038/ng.171 · Cited by 1,054 · see citing works

A common genetic variant is associated with adult and childhood obesity.

Herbert, A., Gerry, N. P., McQueen, M. B., Heid, I. M., Pfeufer, A., Illig, T., Wichmann, H.-E., Meitinger, T., Hunter, D., Hu, F. B., et al. (2006) · Science · doi:10.1126/science.1124779 · Cited by 732 · see citing works

Genome-wide Association Analysis Reveals Putative Alzheimer's Disease Susceptibility Loci in Addition to APOE

Bertram, L., Lange, C., Mullin, K., Parkinson, M., Hsiao, M., Hogan, M. F., Schjeide, B. M. M., Hooli, B., DiVito, J., Ionita, I., et al. (2008) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2008.10.008 · Cited by 511 · see citing works

Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS

Mattheisen, M., Samuels, J. F., Wang, Y., Greenberg, B. D., Fyer, A. J., McCracken, J. T., Geller, D. A., Murphy, D. L., Knowles, J. A., Grados, M. A., et al. (2015) · Molecular Psychiatry · doi:10.1038/mp.2014.43 · Cited by 321 · see citing works

Association study of eight circadian genes with bipolar I disorder, schizoaffective disorder and schizophrenia

Mansour, H. A., Wood, J., Logue, T., Chowdari, K. V., Dayal, M., Kupfer, D. J., Monk, T. H., Devlin, B., & Nimgaonkar, V. L. (2006) · Genes, Brain and Behavior · doi:10.1111/j.1601-183x.2005.00147.x · Cited by 293 · see citing works

The oxytocin receptor (OXTR) contributes to prosocial fund allocations in the dictator game and the social value orientations task

Israel, S., Lerer, E., Shalev, I., Uzefovsky, F., Riebold, M., Laiba, E., Bachner-Melman, R., Maril, A., Bornstein, G., Knafo, A., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005535 · Cited by 278 · see citing works

The influence of serotonin- and other genes on impulsive behavioral aggression and cognitive impulsivity in children with attention-deficit/hyperactivity disorder (ADHD): Findings from a family-based association test (FBAT) analysis

Oades, R. D., Lasky-Su, J., Christiansen, H., Faraone, S. V., Sonuga-Barke, E. J. S., Banaschewski, T., Chen, W., Anney, R. J. L., Buitelaar, J. K., Ebstein, R. P., et al. (2008) · Behavioral and Brain Functions · doi:10.1186/1744-9081-4-48 · Cited by 200 · see citing works

Functional Candidate Genes in Age-Related Macular Degeneration: Significant Association with<i>VEGF</i>,<i>VLDLR</i>, and<i>LRP6</i>

Haines, J. L., Schnetz-Boutaud, N., Schmidt, S., Scott, W. K., Agarwal, A., Postel, E. A., Olson, L., Kenealy, S. J., Hauser, M., Gilbert, J. R., et al. (2006) · Investigative Opthalmology &amp; Visual Science · doi:10.1167/iovs.05-0116 · Cited by 189 · see citing works

The CHRNA5/A3/B4 Gene Cluster Variability as an Important Determinant of Early Alcohol and Tobacco Initiation in Young Adults

Schlaepfer, I. R., Hoft, N. R., Collins, A. C., Corley, R. P., Hewitt, J. K., Hopfer, C. J., Lessem, J. M., McQueen, M. B., Rhee, S. H., & Ehringer, M. A. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.10.024 · Cited by 186 · see citing works

Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophrenia

Mansour, H. A., Talkowski, M. E., Wood, J., Chowdari, K. V., McClain, L., Prasad, K., Montrose, D., Fagiolini, A., Friedman, E. S., Allen, M. H., et al. (2009) · Bipolar Disorders · doi:10.1111/j.1399-5618.2009.00756.x · Cited by 161 · see citing works

Meta‐analysis of association between obsessive‐compulsive disorder and the 3′ region of neuronal glutamate transporter gene <i>SLC1A1</i>

Stewart, S. E., Mayerfeld, C., Arnold, P. D., Crane, J. R., O'Dushlaine, C., Fagerness, J. A., Yu, D., Scharf, J. M., Chan, E., Kassam, F., et al. (2013) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32137 · Cited by 102 · see citing works

Comprehensive family-based association study of the glutamate transporter gene SLC1A1 in obsessive-compulsive disorder

Samuels, J., Wang, Y., Riddle, M. A., Greenberg, B. D., Fyer, A. J., McCracken, J. T., Rauch, S. L., Murphy, D. L., Grados, M. A., Knowles, J. A., et al. (2011) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics · doi:10.1002/ajmg.b.31184 · Cited by 89 · see citing works

Role of common and rare <i>APP</i> DNA sequence variants in Alzheimer disease

Hooli, B. V., Mohapatra, G., Mattheisen, M., Parrado, A. R., Roehr, J. T., Shen, Y., Gusella, J. F., Moir, R., Saunders, A. J., Lange, C., et al. (2012) · Neurology · doi:10.1212/wnl.0b013e3182515972 · Cited by 87 · see citing works

PBAT: A comprehensive software package for genome-wide association analysis of complex family-based studies.

Van Steen, K., & Lange, C. (2005) · Human Genomics · doi:10.1186/1479-7364-2-1-67 · Cited by 73 · see citing works

Association between arginine vasopressin 1a receptor (AVPR1a) promoter region polymorphisms and prepulse inhibition

Levin, R., Heresco-Levy, U., Bachner-Melman, R., Israel, S., Shalev, I., & Ebstein, R. P. (2009) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2008.12.014 · Cited by 68 · see citing works

Association of distinct variants in SORL1 with cerebrovascular and neurodegenerative changes related to Alzheimer disease

Cuenco, K. T. (2008) · Archives of Neurology · doi:10.1001/archneur.65.12.1640 · Cited by 61 · see citing works

Complex effects of dyslexia risk factors account for <scp>ADHD</scp> traits: evidence from two independent samples

Mascheretti, S., Trezzi, V., Giorda, R., Boivin, M., Plourde, V., Vitaro, F., Brendgen, M., Dionne, G., & Marino, C. (2017) · Journal of Child Psychology and Psychiatry · doi:10.1111/jcpp.12612 · Cited by 37 · see citing works

Partial replication of a DRD4 association in ADHD individuals using a statistically derived quantitative trait for ADHD in a family-based association test

Lasky-Su, J., Banaschewski, T., Buitelaar, J., Franke, B., Brookes, K., Sonuga-Barke, E., Ebstein, R., Eisenberg, J., Gill, M., Manor, I., et al. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.03.006 · Cited by 29 · see citing works

Correction to: Hum Gene Ther 2015;26(8):525–537 DOI: 10.1089/hum.2015.064

(2015) · Human Gene Therapy · doi:10.1089/hum.2015.064.cxn

Correction to: Hum Gene Ther 2016;27(1):60-71

(2016) · Human Gene Therapy · doi:10.1089/hum.2015.109.correx

Authors' Response to Jesse D. Riordan, Hum Gene Ther 2017;28:375–376; DOI: 10.1089/hum.2017.045

Srivastava, A., & Carter, B. J. (2017) · Human Gene Therapy · doi:10.1089/hum.2017.050

Challenges posed by hijacked journals in Scopus

Abalkina, A. (2024) · Journal of the Association for Information Science and Technology · doi:10.1002/asi.24855 · Cited by 47 · see citing works

King Range Archaeological Project - Results of the 1984 Field Season, Excavations at CA-HUM-307, HUM-276, HUM-270, and HUM-175

Levulett, V. A., Hildebrandt, W. R., Gilreath, A. J., et al. (1987) · Cited by 3 · see citing works