Dense SNP association study for bipolar I disorder on chromosome 18p11 suggests two loci with excess paternal transmission

A haplotype map of the human genome

2005 • 5,856 citations

NCBI reference sequences (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

2006 • 4,425 citations

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM).

1993 • 3,693 citations

The Risk of Cancer Associated with Specific Mutations ofBRCA1andBRCA2among Ashkenazi Jews

1997 • 2,255 citations

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

2006 • 2,206 citations

NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

2004 • 1,523 citations

The Heritability of Bipolar Affective Disorder and the Genetic Relationship to Unipolar Depression

2003 • 1,188 citations

The effects of human population structure on large genetic association studies

2004 • 888 citations

A missense mutation of the endothelin-B receptor gene in multigenic hirschsprung's disease

1994 • 886 citations

Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia

2002 • 824 citations

A common variant associated with prostate cancer in European and African populations

2006 • 784 citations

A census of mammalian imprinting

2005 • 644 citations

Sample size requirements for matched case‐control studies of gene–environment interaction

2001 • 616 citations

QUANTO 1.1: A computer program for power and sample size calculations for genetic-epidemiology studies

2006 • 609 citations

Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part III: Bipolar Disorder

2003 • 573 citations

BeadArray^™ Technology: Enabling an Accurate, Cost-Effective Approach to High-Throughput Genotyping

2002 • 470 citations

Demonstrating stratification in a European American population

2005 • 449 citations

Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly

2002 • 445 citations

An integrated epigenetic and genetic approach to common human disease

2004 • 442 citations

A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2

1999 • 399 citations

High Concordance of Bipolar I Disorder in a Nationwide Sample of Twins

2004 • 385 citations

Chromosome 18 DNA markers and manic-depressive illness: evidence for a susceptibility gene.

1994 • 378 citations

EPIGENETICS AND HUMAN DISEASE

2004 • 363 citations

Evidence for linkage of bipolar disorder to chromosome 18 with a parent-of-origin effect.

1995 • 347 citations

Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study.

1996 • 337 citations

Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22

1994 • 243 citations

Costs of Bipolar Disorder

2003 • 238 citations

Methods for Detection of Parent-of-Origin Effects in Genetic Studies of Case-Parents Triads

1999 • 233 citations

Haplotype Inference in Random Population Samples

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Endothelin receptor-mediated signaling in hirschsprung disease.

1996 • 177 citations

Chromosome 18 DNA markers and manic-depressive illness : evidence for a susceptibility gene

1994 • 169 citations

Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies

2004 • 154 citations

Probability of Detection of Genotyping Errors and Mutations as Inheritance Inconsistencies in Nuclear-Family Data

2002 • 149 citations

Haplotype and Phenotype Analysis of Nine Recurrent BRCA2 Mutations in 111 Families: Results of an International Study

1998 • 149 citations

Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families

1999 • 129 citations

The Founder Mutation MSH2*1906G→C Is an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Ashkenazi Jewish Population

2002 • 128 citations

Paternal transmission of the very common class I INS VNTR alleles predisposes to childhood obesity

2001 • 117 citations

Genomewide Linkage Scan for Bipolar-Disorder Susceptibility Loci among Ashkenazi Jewish Families

2004 • 95 citations

Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder

2003 • 86 citations

Epigenetics and bipolar disorder: New opportunities and challenges

2003 • 83 citations

A Founder Mutation of the <EMPH TYPE="ITAL">MSH2</EMPH> Gene and Hereditary Nonpolyposis Colorectal Cancer in the United States

2004 • 83 citations

Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder

2003 • 81 citations

The Wellcome trust UK–Irish bipolar affective disorder sibling-pair genome screen: first stage report

2002 • 72 citations

Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with schizophrenia in the Japanese population

2006 • 57 citations

Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder in Japanese and the National Institute of Mental Health pedigrees

2004 • 57 citations

Genomic structure and novel variants of myo-inositol monophosphatase 2 (IMPA2)

2000 • 50 citations

Haplotype and Missing Data Inference in Nuclear Families

2004 • 50 citations

Assessment of the Effect of Age at Onset on Linkage to Bipolar Disorder: Evidence on Chromosomes 18p and 21q

2005 • 48 citations

Alternative transcripts and evidence of imprinting of GNAL on 18p11.2

2005 • 41 citations

Fine-scale mapping of a locus for severe bipolar mood disorder on chromosome 18p11.3 in the Costa Rican population

2001 • 38 citations

Parental transmission and D18S37 allele sharing in bipolar affective disorder

1997 • 31 citations

Linkage disequilibrium analysis of G-olfα (GNAL) in bipolar affective disorder

1996 • 28 citations

Association analysis of the pituitary adenyl cyclase activating peptide gene (PACAP) on chromosome 18p11 with schizophrenia and bipolar disorders

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Analysis of variations in the NAPG gene on chromosome 18p11 in bipolar disorder

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Lack of association between variations in the melanocortin 5 receptor gene and bipolar disorder

2005 • 6 citations