Published in Am J Hum Genet on June 01, 1996
A new statistical method for haplotype reconstruction from population data. Am J Hum Genet (2001) 59.30
Multipoint quantitative-trait linkage analysis in general pedigrees. Am J Hum Genet (1998) 40.97
Genotype imputation. Annu Rev Genomics Hum Genet (2009) 18.64
Family-based association tests for genomewide association scans. Am J Hum Genet (2007) 10.67
In silico method for inferring genotypes in pedigrees. Nat Genet (2006) 7.08
A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait. Am J Hum Genet (2001) 6.56
Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markers. Am J Hum Genet (2005) 6.12
A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set. Am J Hum Genet (2003) 5.34
Detection and integration of genotyping errors in statistical genetics. Am J Hum Genet (2002) 4.89
Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia. Am J Hum Genet (2002) 4.03
Extent and distribution of linkage disequilibrium in three genomic regions. Am J Hum Genet (2000) 3.68
A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome. Neuron (2010) 3.31
A genomewide scan for age-related macular degeneration provides evidence for linkage to several chromosomal regions. Am J Hum Genet (2003) 3.23
Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer. Am J Hum Genet (2004) 3.21
A major lung cancer susceptibility locus maps to chromosome 6q23-25. Am J Hum Genet (2004) 3.05
Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone. Am J Hum Genet (2002) 3.00
Bayesian mapping of multiple quantitative trait loci from incomplete outbred offspring data. Genetics (1999) 2.81
A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27. Am J Hum Genet (2002) 2.74
Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome. Am J Hum Genet (2003) 2.73
Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35. Am J Hum Genet (2004) 2.65
Efficient multipoint linkage analysis through reduction of inheritance space. Am J Hum Genet (2001) 2.58
Caution on pedigree haplotype inference with software that assumes linkage equilibrium. Am J Hum Genet (2002) 2.51
Dissecting the genetic complexity of the association between human leukocyte antigens and rheumatoid arthritis. Am J Hum Genet (2002) 2.47
A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. Am J Hum Genet (1999) 2.38
A general approach for haplotype phasing across the full spectrum of relatedness. PLoS Genet (2014) 2.38
DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Natl Acad Sci U S A (2005) 2.35
Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome). J Med Genet (2005) 2.24
A novel NOD2/CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews. Am J Hum Genet (2003) 2.17
Shared loci for migraine and epilepsy on chromosomes 14q12-q23 and 12q24.2-q24.3. Neurology (2012) 2.09
PedGenie: an analysis approach for genetic association testing in extended pedigrees and genealogies of arbitrary size. BMC Bioinformatics (2006) 2.06
A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1. Am J Hum Genet (2002) 2.04
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. PLoS One (2012) 1.96
Bayesian mapping of quantitative trait loci under complicated mating designs. Genetics (2001) 1.96
Multipoint linkage analysis with many multiallelic or dense diallelic markers: Markov chain-Monte Carlo provides practical approaches for genome scans on general pedigrees. Am J Hum Genet (2006) 1.95
KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron. Nat Genet (2012) 1.93
A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2. Am J Hum Genet (2000) 1.86
Fine mapping of chromosome 6q23-25 region in familial lung cancer families reveals RGS17 as a likely candidate gene. Clin Cancer Res (2009) 1.83
Loss-of-function variants in endothelial lipase are a cause of elevated HDL cholesterol in humans. J Clin Invest (2009) 1.83
Whole-genome screening in ankylosing spondylitis: evidence of non-MHC genetic-susceptibility loci. Am J Hum Genet (2001) 1.82
Mutations in SLC34A2 cause pulmonary alveolar microlithiasis and are possibly associated with testicular microlithiasis. Am J Hum Genet (2006) 1.81
A major susceptibility locus for specific language impairment is located on 13q21. Am J Hum Genet (2002) 1.79
Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11. Am J Hum Genet (1999) 1.78
Kelch-like homologue 9 mutation is associated with an early onset autosomal dominant distal myopathy. Brain (2010) 1.76
The use of family relationships and linkage disequilibrium to impute phase and missing genotypes in up to whole-genome sequence density genotypic data. Genetics (2010) 1.72
Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results. Hum Hered (2009) 1.71
Genetics of microstructure of cerebral white matter using diffusion tensor imaging. Neuroimage (2010) 1.70
Haplotype and missing data inference in nuclear families. Genome Res (2004) 1.69
High-resolution multipoint linkage-disequilibrium mapping in the context of a human genome sequence. Am J Hum Genet (2001) 1.69
Neuropathy target esterase gene mutations cause motor neuron disease. Am J Hum Genet (2008) 1.66
Ethylmalonic encephalopathy is caused by mutations in ETHE1, a gene encoding a mitochondrial matrix protein. Am J Hum Genet (2004) 1.66
Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation. Am J Hum Genet (2000) 1.60
Genome scan for Tourette disorder in affected-sibling-pair and multigenerational families. Am J Hum Genet (2007) 1.60
Collagen type III alpha I is a gastro-oesophageal reflux disease susceptibility gene and a male risk factor for hiatus hernia. Gut (2009) 1.59
A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans. Am J Hum Genet (2006) 1.59
Identification of two novel loci for dominantly inherited familial amyotrophic lateral sclerosis. Am J Hum Genet (2003) 1.56
Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene. Neurology (2012) 1.56
A susceptibility locus for migraine with aura, on chromosome 4q24. Am J Hum Genet (2002) 1.55
Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22. Am J Hum Genet (2004) 1.55
Severe infantile encephalomyopathy caused by a mutation in COX6B1, a nucleus-encoded subunit of cytochrome c oxidase. Am J Hum Genet (2008) 1.54
Mixed model analysis of quantitative trait loci. Proc Natl Acad Sci U S A (2000) 1.54
A visual migraine aura locus maps to 9q21-q22. Neurology (2010) 1.52
SimPed: a simulation program to generate haplotype and genotype data for pedigree structures. Hum Hered (2005) 1.52
Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11. Am J Hum Genet (2004) 1.49
Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney disease. Am J Hum Genet (2001) 1.47
Multilocus lod scores in large pedigrees: combination of exact and approximate calculations. Hum Hered (2007) 1.46
Genome scans provide evidence for low-HDL-C loci on chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families. Am J Hum Genet (2002) 1.45
Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolate. Am J Hum Genet (2003) 1.42
Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci. Am J Hum Genet (2006) 1.41
A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22. Am J Hum Genet (2001) 1.41
Efficient genome ancestry inference in complex pedigrees with inbreeding. Bioinformatics (2010) 1.40
Deficiency of terminal ADP-ribose protein glycohydrolase TARG1/C6orf130 in neurodegenerative disease. EMBO J (2013) 1.40
Genetic studies of stuttering in a founder population. J Fluency Disord (2006) 1.39
Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment. Hum Hered (2004) 1.38
Linkage analysis in the next-generation sequencing era. Hum Hered (2011) 1.37
Linkage of a gene for familial hypobetalipoproteinemia to chromosome 3p21.1-22. Am J Hum Genet (2000) 1.37
The role of large pedigrees in an era of high-throughput sequencing. Hum Genet (2012) 1.37
Identity by descent: variation in meiosis, across genomes, and in populations. Genetics (2013) 1.37
Genome scan for predisposing loci for distal interphalangeal joint osteoarthritis: evidence for a locus on 2q. Am J Hum Genet (1999) 1.35
Multivariate variance-components analysis of longitudinal blood pressure measurements from the Framingham Heart Study. BMC Genet (2003) 1.34
Genome Reshuffling for Advanced Intercross Permutation (GRAIP): simulation and permutation for advanced intercross population analysis. PLoS One (2008) 1.33
CRISPLD2: a novel NSCLP candidate gene. Hum Mol Genet (2007) 1.32
Fine mapping of the alpha-T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees. Hum Mol Genet (2003) 1.32
Evidence for linkage and association with reading disability on 6p21.3-22. Am J Hum Genet (2002) 1.31
Identity by descent estimation with dense genome-wide genotype data. Genet Epidemiol (2011) 1.31
A survey of affected-sibship statistics for nonparametric linkage analysis. Am J Hum Genet (2001) 1.30
Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q. Am J Hum Genet (2001) 1.30
Haplotype mapping of a major quantitative-trait locus for fetal hemoglobin production, on chromosome 6q23. Am J Hum Genet (1998) 1.28
Determinants of variation in human serum paraoxonase activity. Heredity (Edinb) (2008) 1.27
A genomewide search using an original pairwise sampling approach for large genealogies identifies a new locus for total and low-density lipoprotein cholesterol in two genetically differentiated isolates of Sardinia. Am J Hum Genet (2004) 1.24
Analysis of genetic variability and whole genome linkage of whole-brain, subcortical, and ependymal hyperintense white matter volume. Stroke (2009) 1.24
The structure of genetic linkage data: from LIPED to 1M SNPs. Hum Hered (2011) 1.22
Genome-wide linkage scan identifies a novel genetic locus on chromosome 5p13 for neonatal atrial fibrillation associated with sudden death and variable cardiomyopathy. Circulation (2004) 1.21
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39. Am J Hum Genet (2009) 1.21
The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations. Hum Genet (2009) 1.20
A new essential hypertension susceptibility locus on chromosome 2p24-p25, detected by genomewide search. Am J Hum Genet (2002) 1.20
A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q24.3. Hum Genet (2006) 1.19
Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q. Am J Hum Genet (2003) 1.19
Linkage analysis in a large Swedish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 9q22.32-31.1. J Med Genet (2006) 1.18
A frameshift mutation in LRSAM1 is responsible for a dominant hereditary polyneuropathy. Hum Mol Genet (2011) 1.18
Composite statistics for QTL mapping with moderately discordant sibling pairs. Am J Hum Genet (2000) 1.18
Optimization by simulated annealing. Science (1983) 71.02
Strategies for multilocus linkage analysis in humans. Proc Natl Acad Sci U S A (1984) 48.41
Linkage of early-onset familial breast cancer to chromosome 17q21. Science (1990) 16.21
A single ataxia telangiectasia gene with a product similar to PI-3 kinase. Science (1995) 15.20
Programs for Pedigree Analysis: MENDEL, FISHER, and dGENE. Genet Epidemiol (1988) 13.73
The affected-pedigree-member method of linkage analysis. Am J Hum Genet (1988) 13.67
Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome. Genomics (1990) 13.23
A class of tests for linkage using affected pedigree members. Biometrics (1994) 10.40
Metropolis sampling in pedigree analysis. Stat Methods Med Res (1993) 4.04
A Gibbs sampling approach to linkage analysis. Hum Hered (1992) 3.78
A random walk method for computing genetic location scores. Am J Hum Genet (1991) 3.45
Simulation of pedigree genotypes by random walks. Am J Hum Genet (1989) 3.10
A gene for episodic ataxia/myokymia maps to chromosome 12p13. Am J Hum Genet (1994) 2.54
Localization of an ataxia-telangiectasia gene to an approximately 500-kb interval on chromosome 11q23.1: linkage analysis of 176 families by an international consortium. Am J Hum Genet (1995) 2.07
Monte Carlo estimation of variance component models for large complex pedigrees. IMA J Math Appl Med Biol (1991) 2.02
Ataxia-telangiectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndrome. Hum Genet (1992) 1.68
Extensions to pedigree analysis I. Likehood calculations for simple and complex pedigrees. Hum Hered (1975) 16.67
Programs for Pedigree Analysis: MENDEL, FISHER, and dGENE. Genet Epidemiol (1988) 13.73
The affected-pedigree-member method of linkage analysis. Am J Hum Genet (1988) 13.67
EM reconstruction algorithms for emission and transmission tomography. J Comput Assist Tomogr (1984) 6.54
Statistical analysis of multilocus recombination. Biometrics (1983) 6.49
An alternative model of recombination and interference. Ann Hum Genet (1979) 6.26
Estimating kinetic constants from single channel data. Biophys J (1983) 6.14
Extensions to pedigree analysis. III. Variance components by the scoring method. Ann Hum Genet (1976) 5.86
A conditional inference framework for extending the transmission/disequilibrium test. Hum Hered (1998) 5.70
How many polymorphic genes will it take to span the human genome? Am J Hum Genet (1982) 5.11
Computer programs for multilocus haplotyping of general pedigrees. Am J Hum Genet (1995) 4.51
Use of population isolates for mapping complex traits. Nat Rev Genet (2000) 4.28
An algorithm for automatic genotype elimination. Am J Hum Genet (1987) 4.18
Metropolis sampling in pedigree analysis. Stat Methods Med Res (1993) 4.04
Prostate cancer susceptibility locus on chromosome 1q: a confirmatory study. J Natl Cancer Inst (1997) 3.92
Localization of an ataxia-telangiectasia gene to chromosome 11q22-23. Nature (1988) 3.82
The role of early HIV infection in the spread of HIV through populations. J Acquir Immune Defic Syndr Hum Retrovirol (1997) 3.75
Extensions to pedigree analysis. V. Optimal calculation of Mendelian likelihoods. Hum Hered (1983) 3.74
The affected sib-pair method using identity by state relations. Am J Hum Genet (1986) 3.63
Single-sperm typing: determination of genetic distance between the G gamma-globin and parathyroid hormone loci by using the polymerase chain reaction and allele-specific oligomers. Proc Natl Acad Sci U S A (1989) 3.50
The prior probability of autosomal linkage. Ann Hum Genet (1975) 3.45
A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data. Am J Hum Genet (2000) 3.22
Extensions to pedigree analysis. IV. Covariance components models for multivariate traits. Am J Med Genet (1983) 3.10
Statistical analysis of single sodium channels. Effects of N-bromoacetamide. Biophys J (1984) 3.01
EM algorithms without missing data. Stat Methods Med Res (1997) 2.39
The calcium scare--what would Austin Bradford Hill have thought? Osteoporos Int (2011) 2.35
A single dominant gene can account for eye tracking dysfunctions and schizophrenia in offspring of discordant twins. Arch Gen Psychiatry (1988) 2.21
Statistical methods for multipoint radiation hybrid mapping. Am J Hum Genet (1991) 2.16
Fast computation of genetic likelihoods on human pedigree data. Hum Hered (1992) 2.15
Localization of an ataxia-telangiectasia gene to an approximately 500-kb interval on chromosome 11q23.1: linkage analysis of 176 families by an international consortium. Am J Hum Genet (1995) 2.07
Application of a recombination model in calculating the variance of sib pair genetic identity. Ann Hum Genet (1979) 2.01
Ataxia-telangiectasia: an interdisciplinary approach to pathogenesis. Medicine (Baltimore) (1991) 1.89
Ascertainment and goodness of fit of variance component models for pedigree data. Prog Clin Biol Res (1984) 1.89
Nephritis caused by Streptococcus zooepidemicus (Lancefield group C). Lancet (1983) 1.86
Accurate and superaccurate gene mapping. Am J Hum Genet (1985) 1.85
Stimulation of human leukocyte thromboplastic activity by endotoxin. Proc Soc Exp Biol Med (1971) 1.79
Multipoint linkage map of the human pseudoautosomal region, based on single-sperm typing: do double crossovers occur during male meiosis? Am J Hum Genet (1994) 1.78
Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups. Am J Hum Genet (2001) 1.72
Routine immunohistology in renal diseases. Ann Intern Med (1966) 1.69
Ordering three DNA polymorphisms on human chromosome 3 by sperm typing. Genomics (1991) 1.69
The genetic transmission of schizophrenia: application of Mendelian latent structure analysis to eye tracking dysfunctions in schizophrenia and affective disorder. J Psychiatr Res (1986) 1.65
Sensor-augmented pump therapy from the diagnosis of childhood type 1 diabetes: results of the Paediatric Onset Study (ONSET) after 12 months of treatment. Diabetologia (2010) 1.48
A theoretical study of some maximum likelihood algorithms for emission and transmission tomography. IEEE Trans Med Imaging (1987) 1.48
Preliminary ranking procedures for multilocus ordering. Genomics (1987) 1.45
Multilocus ordering strategies based on sperm typing. Ann Hum Genet (1990) 1.40
Two models for a maternal factor in the inheritance of Huntington disease. Am J Hum Genet (1983) 1.37
A goodness-of-fit test for the polygenic threshold model: application to pyloric stenosis. Am J Med Genet (1978) 1.37
Application of the lod method to the detection of linkage between a quantitative trait and a qualitative marker: a simulation experiment. Am J Hum Genet (1976) 1.37
Approximate confidence intervals for risk prediction in genetic counseling. Am J Hum Genet (1986) 1.31
Gamete-competition models. Am J Hum Genet (2000) 1.28
A multilocus extension of the affected-pedigree-member method of linkage analysis. Am J Hum Genet (1992) 1.26
Trials, tribulations, and triumphs of the EM algorithm in pedigree analysis. IMA J Math Appl Med Biol (1989) 1.25
A primary linkage map of the human chromosome 11q22-23 region. Genomics (1990) 1.25
Experimental design and error detection for polyploid radiation hybrid mapping. Genome Res (1995) 1.24
A new class of organic nitrates: investigations on bioactivation, tolerance and cross-tolerance phenomena. Br J Pharmacol (2009) 1.24
Partial characterization of antigenic streptococcal plasma membrane components in acute glomerulonephritis. J Clin Invest (1970) 1.20
Effects of reproductive compensation and genetic drift on X-linked lethals. Am J Hum Genet (1978) 1.20
Ethanol stimulates formation of leukotriene C4 in rat gastric mucosa. Prostaglandins (1986) 1.19
Grouped-coordinate ascent algorithms for penalized-likelihood transmission image reconstruction. IEEE Trans Med Imaging (1997) 1.18
Penalized regression for genome-wide association screening of sequence data. Pac Symp Biocomput (2011) 1.17
Multipoint mapping calculations for sperm-typing data. Am J Hum Genet (1994) 1.16
Evidence for the in situ origin of poststreptococcal glomerulonephritis: glomerular localization of endostreptosin and the clinical significance of the subsequent antibody response. Clin Nephrol (1983) 1.16
Comments on lack of interference in the four strand model of crossing over. J Math Biol (1977) 1.15
Computational advances in maximum likelihood methods for molecular phylogeny. Genome Res (1998) 1.15
Relative-to-relative transition probabilities for two linked genes. Theor Popul Biol (1974) 1.13
A hitherto unknown streptococcal antigen and its probable relation to acute poststreptococcal glomerulonephritis. Clin Nephrol (1976) 1.11
Further mapping of an ataxia-telangiectasia locus to the chromosome 11q23 region. Am J Hum Genet (1990) 1.10
Genomic and functional analyses of Rhodococcus equi phages ReqiPepy6, ReqiPoco6, ReqiPine5, and ReqiDocB7. Appl Environ Microbiol (2010) 1.09
Evidence for the aetiology of injuries in Australian football. Br J Sports Med (2001) 1.08
Antigenic streptococcal components in acute glomerulonephritis. Science (1969) 1.07
Health-related quality of life in chronic pancreatitis: a psychometric assessment. Scand J Gastroenterol (2003) 1.07
Selected locus and multiple panel models for radiation hybrid mapping. Am J Hum Genet (1996) 1.06
Gastric emptying of a liquid nutrient meal in the critically ill: relationship between scintigraphic and carbon breath test measurement. Gut (2011) 1.04
[Brain carbohydrate metabolism following blockade of the pentose phosphate pathway by 6-aminonicotinamide]. Hoppe Seylers Z Physiol Chem (1970) 1.03
Assessment of chronic gamma radiosensitivity as an in vitro assay for heterozygote identification of ataxia-telangiectasia. Radiat Res (1991) 1.03
Brain disorders induced by pharmacological blockade of the pentose phosphate pathway. Biochem Biophys Res Commun (1969) 1.03
Estimation of the variance components for dermal ridge count. Ann Hum Genet (1977) 1.02
Maximum likelihood estimates for fate map locations of behavior in Drosophila. Dev Biol (1974) 1.01
Frequency of Duchenne muscular dystrophy carriers. Lancet (1977) 1.00
Univariate and bivariate analyses of cholesterol and triglyceride levels in pedigrees. Am J Med Genet (1986) 1.00
Reducing glycaemic variability in type 1 diabetes self-management with a continuous glucose monitoring system based on wired enzyme technology. Diabetologia (2009) 0.99
Fishing for pleiotropic QTLs in a polygenic sea. Ann Hum Genet (2005) 0.97
Glomerular lesions in a strain of genetically diabetic mice. Proc Soc Exp Biol Med (1968) 0.96
Osteitis in early syphilis. A case report. Br J Vener Dis (1981) 0.96
Extensions to pedigree analysis. II. Recurrence risk calculation under the polygenic threshold model. Hum Hered (1976) 0.96
Relevance of two-stage total hepatectomy and liver transplantation in acute liver failure and severe liver trauma. Transpl Int (2001) 0.96
Genetic haplotyping of ataxia-telangiectasia families localizes the major gene to an approximately 850 kb region on chromosome 11q23.1. Int J Radiat Biol (1994) 0.96
Sex differences in recombination fraction estimates and their effect on ordering of chromosome 11 markers. Genet Epidemiol Suppl (1986) 0.96
General practitioners' knowledge of and attitudes to inflammatory bowel disease. Intern Med J (2012) 0.95
Renal lesions in narcotic addicts. Am J Med (1974) 0.95
Epidemic glomerulonephritis in Maracaibo. Evidence for progression to chronicity. Clin Nephrol (1976) 0.95
Quantification of mRNA of tyrosine hydroxylase and aromatic L-amino acid decarboxylase in the substantia nigra in Parkinson's disease and schizophrenia. J Neural Transm Park Dis Dement Sect (1994) 0.95
Some combinatorial problems of DNA restriction fragment length polymorphisms. Am J Hum Genet (1983) 0.95
Number of nitrate groups determines reactivity and potency of organic nitrates: a proof of concept study in ALDH-2-/- mice. Br J Pharmacol (2007) 0.94
On Ewens' equivalence theorem for ascertainment sampling schemes. Am J Hum Genet (1983) 0.94
Effects of non-steroidal anti-inflammatory drugs on rat gastric mucosal leukotriene C4 and prostanoid release: relation to ethanol-induced injury. Br J Pharmacol (1988) 0.93
Transketolase activity in uremia. Arch Intern Med (1970) 0.93
SNPs and snails and puppy dogs' tails: analysis of SNP haplotype data using the gamete competition model. Ann Hum Genet (2001) 0.93
The glomerulopathy of congenital syphilis. A curable immune-deposit disease. JAMA (1974) 0.92
Genetic mapping of complex traits: promises, problems, and prospects. Theor Popul Biol (2000) 0.91