Eric D. Green

Q: What Schools Are Affiliated With Eric D. Green

Eric D. Green is affiliated with the following schools: Washington University in St. Louis, University of Wisconsin–Madison, Cardiff University, Pennsylvania State University, University of Birmingham

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Eric D. Green

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#521

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#573

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#190

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World Rank

#180

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#61

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Why Is Eric D. Green Influential?

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According to Wikipedia, Eric D. Green is an American genomics researcher who had significant involvement in the Human Genome Project. He is the director of the National Human Genome Research Institute at the National Institutes of Health , a position he has held since 2009.

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Eric D. Green's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

A global reference for human genetic variation (2015) (11857)
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (2007) (9208)
An integrated map of genetic variation from 1,092 human genomes (2012) (7565)
The Genotype-Tissue Expression (GTEx) project (2013) (6030)
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007) (5196)
Initial sequencing and comparative analysis of the mouse genome. (2002) (4609)
Topographical and Temporal Diversity of the Human Skin Microbiome (2009) (2258)
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome (1995) (2242)
The ENCODE (ENCyclopedia Of DNA Elements) Project (2004) (2194)
An integrated encyclopedia of DNA elements in the human genome (2012) (2080)
Genome sequence of the Brown Norway rat yields insights into mammalian evolution (2004) (2053)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (2013) (2011)
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences (2002) (1846)
A vision for the future of genomics research (2003) (1746)
A User's Guide to the Encyclopedia of DNA Elements (ENCODE) (2011) (1467)
Aligning multiple genomic sequences with the threaded blockset aligner. (2004) (1439)
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants (2007) (1421)
Distribution and intensity of constraint in mammalian genomic sequence. (2005) (1275)
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder (2008) (1189)
Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS) (1997) (1147)
LAGAN and Multi-LAGAN: efficient tools for large-scale multiple alignment of genomic DNA. (2003) (1131)
A high-resolution map of human evolutionary constraint using 29 mammals (2011) (1081)
Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder (2017) (998)
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 (2011) (929)
Charting a course for genomic medicine from base pairs to bedside (2011) (846)
A physical map of the human genome (2001) (753)
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) (676)
Comparative analyses of multi-species sequences from targeted genomic regions (2003) (666)
Defining functional DNA elements in the human genome (2014) (647)
Mutations in TWIST, a basic helix–loop–helix transcription factor, in Saethre-Chotzen syndrome (1997) (635)
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (600)
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (2004) (565)
LIM-kinase1 Hemizygosity Implicated in Impaired Visuospatial Constructive Cognition (1996) (530)
Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V. (2003) (526)
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (2017) (517)
Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion (2001) (514)
The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia (2009) (508)
Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (465)
Implementing genomic medicine in the clinic: the future is here (2013) (463)
A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk (2005) (457)
The DNA sequence of human chromosome 7 (2003) (425)
Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction. (1990) (420)
Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder. (2009) (412)
Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells. (2000) (411)
High throughput fingerprint analysis of large-insert clones. (1997) (410)
Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome. (2001) (392)
Patterns of somatic structural variation in human cancer genomes (2020) (377)
Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk (2009) (375)
A mutation in PDS causes non-syndromic recessive deafness (1998) (372)
The asparagine-linked oligosaccharides on bovine fetuin. Structural analysis of N-glycanase-released oligosaccharides by 500-megahertz 1H NMR spectroscopy. (1988) (365)
Meiotic arrest and aneuploidy in MLH3-deficient mice (2002) (363)
Identification and characterization of multi-species conserved sequences. (2003) (356)
Disruption of an AP-2α binding site in an IRF6 enhancer is strongly associated with cleft lip (2008) (355)
Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1). (1999) (348)
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum (2011) (337)
Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear. (1999) (324)
The human pregnane X receptor: genomic structure and identification and functional characterization of natural allelic variants. (2001) (299)
Transcription-associated mutational asymmetry in mammalian evolution (2003) (291)
Pituitary glycoprotein hormone oligosaccharides: structure, synthesis and function of the asparagine-linked oligosaccharides on lutropin, follitropin and thyrotropin. (1988) (286)
Asparagine-linked oligosaccharides on lutropin, follitropin, and thyrotropin. I. Structural elucidation of the sulfated and sialylated oligosaccharides on bovine, ovine, and human pituitary glycoprotein hormones. (1988) (284)
The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine. (2009) (262)
Targets of balancing selection in the human genome. (2009) (261)
The role of aminoacyl-tRNA synthetases in genetic diseases. (2008) (259)
Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorder. (2005) (255)
The human obese (OB) gene: RNA expression pattern and mapping on the physical, cytogenetic, and genetic maps of chromosome 7. (1995) (255)
MultiPipMaker and supporting tools: alignments and analysis of multiple genomic DNA sequences (2003) (254)
Cytogenetic and molecular delineation of a region of chromosome 7 commonly deleted in malignant myeloid diseases. (1996) (251)
The National Institutes of Health's Big Data to Knowledge (BD2K) initiative: capitalizing on biomedical big data (2014) (248)
Prioritizing diversity in human genomics research (2017) (246)
Long noncoding RNA genes: conservation of sequence and brain expression among diverse amniotes (2010) (246)
Confirming the Phylogeny of Mammals by Use of Large Comparative Sequence Data Sets (2008) (243)
Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model (2004) (233)
Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome. (2007) (221)
Balancing Selection Maintains a Form of ERAP2 that Undergoes Nonsense-Mediated Decay and Affects Antigen Presentation (2010) (220)
Chromosomal region of the cystic fibrosis gene in yeast artificial chromosomes: a model for human genome mapping. (1990) (214)
The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder. (2000) (212)
Deoxycorticosterone Upregulates PDS (Slc26a4) in Mouse Kidney: Role of Pendrin in Mineralocorticoid-Induced Hypertension (2003) (211)
Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing. (2010) (209)
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
Regulatory divergence modifies limb length between mammals. (2008) (203)
Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC (2013) (200)
Fluorescence in situ hybridization of YAC clones after Alu-PCR amplification. (1992) (199)
Comprehensive molecular characterization of mitochondrial genomes in human cancers (2017) (197)
Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries. (2011) (196)
Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia. (2010) (192)
Genome analysis : a laboratory manual (1997) (192)
Identifying gene regulatory elements by genome-wide recovery of DNase hypersensitive sites. (2004) (191)
Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathy. (2010) (188)
Global implementation of genomic medicine: We are not alone (2015) (183)
NaCl Restriction Upregulates Renal Slc26a4 Through Subcellular Redistribution: Role in Cl− Conservation (2004) (183)
Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins. (2002) (181)
Two frequent missense mutations in Pendred syndrome. (1998) (179)
Extreme Obesity May Be Linked to Markers Flanking the Human OB Gene (1996) (175)
Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder (2011) (173)
Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia (2006) (172)
Human Genome Project: Twenty-five years of big biology (2015) (171)
Large-scale sequencing of the CD33-related Siglec gene cluster in five mammalian species reveals rapid evolution by multiple mechanisms. (2004) (159)
Reconstructing large regions of an ancestral mammalian genome in silico. (2004) (158)
Genetic variation of brain-derived neurotrophic factor (BDNF) in bipolar disorder (2006) (157)
Analysis of primate genomic variation reveals a repeat-driven expansion of the human genome. (2003) (156)
Copy number variation in bipolar disorder (2015) (154)
Detection and characterization of chimeric yeast artificial-chromosome clones. (1991) (154)
Pendrin is an iodide-specific apical porter responsible for iodide efflux from thyroid cells. (2002) (154)
Localization of pendrin in mouse kidney. (2003) (154)
Strategies for the systematic sequencing of complex genomes (2001) (153)
Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder. (2006) (148)
Molecular anatomy of chromosome 7q deletions in myeloid neoplasms: evidence for multiple critical loci. (1998) (147)
VarSifter: Visualizing and analyzing exome-scale sequence variation data on a desktop computer (2012) (146)
Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case–control sample (2013) (145)
The human reelin gene: isolation, sequencing, and mapping on chromosome 7. (1997) (144)
Quantitative estimates of sequence divergence for comparative analyses of mammalian genomes. (2003) (139)
Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder (2017) (136)
An initial strategy for the systematic identification of functional elements in the human genome by low-redundancy comparative sequencing. (2005) (135)
Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype (2008) (135)
Localization and Functional Studies of Pendrin in the Mouse Inner Ear Provide Insight About the Etiology of Deafness in Pendred Syndrome (2003) (134)
The completion of the Mammalian Gene Collection (MGC). (2009) (132)
Evidence that duplications of 22q11.2 protect against schizophrenia (2013) (130)
Strategic vision for improving human health at The Forefront of Genomics (2020) (130)
A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease. (1997) (130)
Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia (2017) (129)
A family of mammalian anion transporters and their involvement in human genetic diseases. (1999) (128)
Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations. (2005) (128)
Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes (1998) (127)
Structural elucidation of the disulfated oligosaccharide from bovine lutropin. (1985) (125)
Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD (2005) (123)
The genomic region encompassing the nephropathic cystinosis gene (CTNS): complete sequencing of a 200-kb segment and discovery of a novel gene within the common cystinosis-causing deletion. (2000) (121)
Genomics education for health care professionals in the 21st century. (2011) (118)
The value of avian genomics to the conservation of wildlife (2009) (117)
Lack of pendrin HCO3- transport elevates vestibular endolymphatic [Ca2+] by inhibition of acid-sensitive TRPV5 and TRPV6 channels. (2007) (117)
Sequence-tagged site (STS) content mapping of human chromosomes: theoretical considerations and early experiences. (1991) (115)
Meta-analysis of two genome-wide association studies of bipolar disorder reveals important points of agreement (2008) (115)
The Complexities of Genomic Identifiability (2013) (113)
Functional Analyses of Glycyl-tRNA Synthetase Mutations Suggest a Key Role for tRNA-Charging Enzymes in Peripheral Axons (2006) (112)
Identification of Neural Crest and Glial Enhancers at the Mouse Sox10 Locus through Transgenesis in Zebrafish (2008) (111)
Gene therapy rescues cilia defects and restores olfactory function in a mammalian ciliopathy model (2012) (110)
Construction of a 2.6-Mb contig in yeast artificial chromosomes spanning the human dystrophin gene using an STS-based approach. (1992) (109)
Charcot-Marie-Tooth–Linked Mutant GARS Is Toxic to Peripheral Neurons Independent of Wild-Type GARS Levels (2011) (107)
Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1) (2005) (107)
Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndrome. (1998) (104)
MLL5, a homolog of Drosophila trithorax located within a segment of chromosome band 7q22 implicated in myeloid leukemia (2002) (103)
Direct interaction of Sox10 with the promoter of murine Dopachrome Tautomerase (Dct) and synergistic activation of Dct expression with Mitf. (2004) (103)
A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene (2009) (101)
Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness. (2006) (100)
Asparagine-linked oligosaccharides on lutropin, follitropin, and thyrotropin. II. Distributions of sulfated and sialylated oligosaccharides on bovine, ovine, and human pituitary glycoprotein hormones. (1988) (99)
The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls (2018) (99)
Bipolar affective puerperal psychosis: genome-wide significant evidence for linkage to chromosome 16. (2007) (99)
Gene‐environment interplay in common complex diseases: forging an integrative model—recommendations from an NIH workshop (2011) (99)
A preliminary comparative analysis of primate segmental duplications shows elevated substitution rates and a great-ape expansion of intrachromosomal duplications. (2006) (98)
The consistent association between Epstein-Barr virus and Hodgkin's disease in children in Kenya. (1996) (96)
Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept (2009) (96)
Retention of pendrin in the endoplasmic reticulum is a major mechanism for Pendred syndrome. (2002) (96)
Reduced ENaC protein abundance contributes to the lower blood pressure observed in pendrin-null mice. (2007) (95)
A physical map of human chromosome 7: an integrated YAC contig map with average STS spacing of 79 kb. (1997) (94)
Oligosaccharide specificities of Phaseolus vulgaris leukoagglutinating and erythroagglutinating phytohemagglutinins. Interactions with N-glycanase-released oligosaccharides. (1987) (93)
Association at SYNE1 in both bipolar disorder and recurrent major depression (2013) (93)
Research Directions in the Clinical Implementation of Pharmacogenomics: An Overview of US Programs and Projects (2018) (93)
Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research (2017) (92)
Lectin affinity high-performance liquid chromatography. Interactions of N-glycanase-released oligosaccharides with Ricinus communis agglutinin I and Ricinus communis agglutinin II. (1987) (91)
Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genes. (2000) (89)
Progressive proximal expansion of the primate X chromosome centromere. (2005) (88)
Evaluation of the RET regulatory landscape reveals the biological relevance of a HSCR-implicated enhancer. (2005) (88)
Mutational and functional analyses reveal that ST7 is a highly conserved tumor-suppressor gene on human chromosome 7q31 (2001) (87)
Systematic generation of sequence-tagged sites for physical mapping of human chromosomes: application to the mapping of human chromosome 7 using yeast artificial chromosomes. (1991) (86)
Metaphase and interphase cytogenetics with Alu-PCR-amplified yeast artificial chromosome clones containing the BCR gene and the protooncogenes c-raf-1, c-fms, and c-erbB-2. (1992) (86)
Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig. (1995) (86)
Dietary Cl(-) restriction upregulates pendrin expression within the apical plasma membrane of type B intercalated cells. (2006) (83)
Comparative sequencing provides insights about the structure and conservation of marsupial and monotreme genomes. (2005) (82)
Sequencing and analysis of 10,967 full-length cDNA clones from Xenopus laevis and Xenopus tropicalis reveals post-tetraploidization transcriptome remodeling. (2006) (82)
An intermediate grade of finished genomic sequence suitable for comparative analyses. (2004) (80)
Genomic structure, chromosomal localization, start of transcription, and tissue expression of the human p40-phox, a new component of the nicotinamide adenine dinucleotide phosphate-oxidase complex. (1996) (80)
Comparative mapping of the region of human chromosome 7 deleted in williams syndrome. (1999) (78)
Progressive sensorineural hearing loss and a widened vestibular aqueduct in Pendred syndrome. (1998) (78)
Cytogenetic and molecular characterization of random chromosomal rearrangements activating the drug resistance gene, MDR1/P‐glycoprotein, in drug‐selected cell lines and patients with drug refractory ALL (1998) (77)
Leukocyte adhesion deficiency (LAD) type II/carbohydrate deficient glycoprotein (CDG) IIc founder effect and genotype/phenotype correlation. (2002) (77)
Results of a genome‐wide linkage scan for stuttering (2004) (77)
Identification and detection of the common 65-kb deletion breakpoint in the nephropathic cystinosis gene (CTNS). (1999) (75)
Recurrent duplication-driven transposition of DNA during hominoid evolution (2006) (75)
Deletion of long-range sequences at Sox10 compromises developmental expression in a mouse model of Waardenburg-Shah (WS4) syndrome. (2006) (73)
Adaptive evolution of foundation kinetochore proteins in primates. (2010) (72)
Identification of Pendrin as a Common Mediator for Mucus Production in Bronchial Asthma and Chronic Obstructive Pulmonary Disease1 (2008) (72)
Comparative sequence analyses reveal rapid and divergent evolutionary changes of the WFDC locus in the primate lineage. (2007) (72)
Mechanism of iodide/chloride exchange by pendrin. (2004) (71)
Generation and Comparative Analysis of ∼3.3 Mb of Mouse Genomic Sequence Orthologous to the Region of Human Chromosome 7q11.23 Implicated in Williams Syndrome (2002) (71)
The NIH Big Data to Knowledge (BD2K) initiative (2015) (71)
Detailed mapping of a congenital heart disease gene in chromosome 3p25 (2000) (70)
Polygenic dissection of the bipolar phenotype (2011) (70)
Genomic medicine for undiagnosed diseases (2019) (69)
Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder (2015) (68)
Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder (2015) (68)
Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC (2013) (67)
An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval. (2014) (67)
Organization of the gene encoding the human Kell blood group protein. (1995) (66)
Specific inactivation of two immunomodulatory SIGLEC genes during human evolution (2012) (66)
Evidence for familial cosegregation of major affective disorder and genetic markers flanking the gene for Darier's disease (2002) (66)
No support for association between Dyslexia Susceptibility 1 Candidate 1 and developmental dyslexia (2005) (65)
Parallel construction of orthologous sequence-ready clone contig maps in multiple species. (2002) (65)
Macrophage invasion contributes to degeneration of stria vascularis in Pendred syndrome mouse model (2006) (64)
Structural organization of the human PON1 gene. (1996) (63)
Expression of PDS/Pds, the Pendred syndrome gene, in endometrium. (2002) (62)
Positional cloning, association analysis and expression studies provide convergent evidence that the cadherin gene FAT contains a bipolar disorder susceptibility allele (2006) (62)
Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (61)
Distinct retroelement classes define evolutionary breakpoints demarcating sites of evolutionary novelty (2009) (61)
Systematic sequencing of cDNA clones using the transposon Tn5. (2002) (60)
Health behavior change: can genomics improve behavioral adherence? (2012) (58)
Computational and experimental analyses reveal previously undetected coding exons of the KRIT1 (CCM1) gene. (2001) (57)
P2RX7: A bipolar and unipolar disorder candidate susceptibility gene? (2009) (57)
Gpnmb is a melanoblast‐expressed, MITF‐dependent gene (2009) (56)
Localization of bipolar susceptibility locus by molecular genetic analysis of the chromosome 12q23-q24 region in two pedigrees with bipolar disorder and Darier's disease. (2005) (55)
Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin (2004) (55)
Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome. (2002) (55)
Are interleukin-1 gene polymorphisms risk factors or disease modifiers in AD? (2002) (54)
Effects of thyroglobulin and pendrin on iodide flux through the thyrocyte (2001) (54)
Integration of physical, genetic and cytogenetic maps of human chromosome 7: isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markers. (1994) (54)
Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome (1999) (51)
Isolation and analysis of candidate myeloid tumor suppressor genes from a commonly deleted segment of 7q22. (2005) (50)
Opportunities, resources, and techniques for implementing genomics in clinical care (2019) (49)
Relevance of genomics to healthcare and nursing practice. (2013) (49)
Childhood-onset schizophrenia/autistic disorder and t(1;7) reciprocal translocation: identification of a BAC contig spanning the translocation breakpoint at 7q21. (2000) (49)
Characterizing genetic variants for clinical action (2014) (48)
Differences between pair-wise and multi-sequence alignment methods affect vertebrate genome comparisons. (2006) (48)
Sulfation of lutropin oligosaccharides with a cell-free system. (1984) (47)
Candidate gene isolation and comparative analysis of a commonly deleted segment of 7q22 implicated in myeloid malignancies. (2001) (45)
Isolation, genomic structure and developmental expression of Fgf8 in the short-tailed fruit bat, Carollia perspicillata. (2007) (45)
A systematic, high-resolution linkage of the cytogenetic and physical maps of the human genome (2000) (45)
Intercalated cell H+/OH- transporter expression is reduced in Slc26a4 null mice. (2005) (44)
Affective temperaments across the bipolar-unipolar spectrum: examination of the TEMPS-A in 927 patients and controls. (2010) (43)
Separation of anionic oligosaccharides by high-performance liquid chromatography. (1986) (43)
Evolution of siglec-11 and siglec-16 genes in hominins. (2012) (43)
Positional candidate genes for congenital chloride diarrhea suggested by high-resolution physical mapping in chromosome region 7q31. (1996) (43)
Lectin affinity high-performance liquid chromatography: interactions of N-glycanase-released oligosaccharides with leukoagglutinating phytohemagglutinin, concanavalin A, Datura stramonium agglutinin, and Vicia villosa agglutinin. (1987) (43)
The human Y4 small cytoplasmic RNA gene is controlled by upstream elements and resides on chromosome 7 with all other hY scRNA genes. (1994) (43)
A human chromosome 7 yeast artificial chromosome (YAC) resource: construction, characterization, and screening. (1995) (42)
Gene expression profiles in acute myeloid leukemia with common translocations using SAGE. (2006) (42)
Loss of KCNJ 10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model (41)
Stage 2 of the Wellcome Trust UK–Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16–q21, 4q12–q21, 9p21, 10p14–p12 and 18q22 (2005) (41)
Sex differences in oncogenic mutational processes (2019) (41)
Definitive functional evidence for a tumor suppressor gene on human chromosome 7q31.1 neighboring the Fra7G site (2000) (41)
The future of DNA sequencing (2017) (39)
A polymorphic variation in the interleukin 1A gene increases brain microglial cell activity in Alzheimer’s disease (2004) (38)
Phenotype-genotype correlation in Hirschsprung disease is illuminated by comparative analysis of the RET protein sequence. (2005) (38)
Cell-free sulfation of human and bovine pituitary hormones. Comparison of the sulfated oligosaccharides of lutropin, follitropin, and thyrotropin. (1985) (38)
Pericentromeric duplications in the laboratory mouse. (2003) (37)
Biosynthesis of sulfated asparagine-linked oligosaccharides on bovine lutropin. (1986) (37)
Brain-derived neurotrophic factor as a potential risk locus for bipolar disorder: Evidence, limitations, and implications (2004) (37)
Meiotic recombination between yeast artificial chromosomes yields a single clone containing the entire BCL2 protooncogene. (1990) (37)
Gene encoding human Ro-associated autoantigen Y5 RNA. (1996) (36)
Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases (2018) (36)
Identification of high risk DISC1 protein structural variants in patients with bipolar spectrum disorder (2010) (35)
Genome Wide Linkage Analysis of 972 Bipolar Pedigrees Using Single Nucleotide Polymorphisms (2011) (35)
Novel human α1a-adrenoceptor single nucleotide polymorphisms alter receptor pharmacology and biological function (2005) (35)
Comparative genome mapping in the sequence-based era: early experience with human chromosome 7. (2000) (34)
Multi-species sequence comparison reveals dynamic evolution of the elastin gene that has involved purifying selection and lineage-specific insertions/deletions (2004) (34)
Evidence that a DISC1 frame-shift deletion associated with psychosis in a single family may not be a pathogenic mutation (2006) (34)
Structural requirements for sulfation of asparagine-linked oligosaccharides of lutropin. (1985) (34)
Stage 2 of the Wellcome Trust UK–Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16–q21, 4q12–q21, 9p21, 10p14–p12 and 18q22 (2006) (34)
Edinburgh Research Explorer Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip (2018) (33)
Computational reconstruction of ancestral DNA sequences. (2008) (33)
Comparative sequence analyses reveal sites of ancestral chromosomal fusions in the Indian muntjac genome (2008) (33)
Assessing mapping progress in the Human Genome Project. (1994) (32)
Phenazopyridine hydrochloride toxicity: a cause of drug-induced methemoglobinemia. (1979) (32)
Recent Selection Changes in Human Genes under Long-Term Balancing Selection. (2016) (32)
The parathyroid hormone-responsive B1 gene is interrupted by a t(1;7)(q42;p15) breakpoint associated with Wilms' tumour (2003) (31)
Genomic structure of the PIK3CG gene on chromosome band 7q22 and evaluation as a candidate myeloid tumor suppressor. (2002) (31)
Identification of the Otopetrin Domain, a conserved domain in vertebrate otopetrins and invertebrate otopetrin-like family members (2008) (30)
Genomics Reaches the Clinic: From Basic Discoveries to Clinical Impact (2011) (30)
No association between CHRNA7 microsatellite markers and attention-deficit hyperactivity disorder. (2001) (30)
A collection of 1814 human chromosome 7-specific STSs. (1997) (29)
Genomic variation in multigenic traits: Hirschsprung disease. (2003) (29)
Disruption of Visc-2, a Brain-Expressed Conserved Long Noncoding RNA, Does Not Elicit an Overt Anatomical or Behavioral Phenotype (2014) (29)
The human genome project. Prospects and implications for clinical medicine. (1991) (29)
Characterization of oligosaccharides by lectin affinity high-performance liquid chromatography. (1989) (29)
Linkage disequilibrium mapping of bipolar affective disorder at 12q23‐q24 provides evidence for association at CUX2 and FLJ32356 (2005) (28)
Clonal Diversity of Ig and T-Cell-Receptor Gene Rearrangements Identifies a Subset of Childhood B-Precursor Acute Lymphoblastic Leukemia With Increased Risk of Relapse (1998) (28)
Novel ATP2A2 mutations in a large sample of individuals with Darier disease (2013) (27)
Integrative DNA, RNA, and protein evidence connects TREML4 to coronary artery calcification. (2014) (27)
Divergent human and mouse orthologs of a novel gene (WBSCR15/Wbscr15) reside within the genomic interval commonly deleted in Williams syndrome (2000) (26)
Leading the way to genomic medicine (2014) (26)
The human genome sequence expedition: views from the "base camp". (2001) (26)
Identification of a potential Bipolar risk haplotype in the gene encoding the winged-helix transcription factor RFX4 (2005) (26)
Evidence that the Saethre-Chotzen syndrome locus lies between D7S664 and D7S507, by genetic analysis and detection of a microdeletion in a patient. (1994) (26)
Characterization of the complete genomic structure of human thromboxane synthase gene and functional analysis of its promoter. (1996) (25)
Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage‐dependent calcium channels in psychiatric disorders (2012) (25)
A structurally aberrant immunoglobulin paraprotein in a patient with multiple myeloma and corneal crystal deposits. (1990) (24)
DISC1 exon 11 rare variants found more commonly in schizoaffective spectrum cases than controls (2011) (24)
Comparative sequence analysis of primate subtelomeres originating from a chromosome fission event. (2009) (23)
Differential processing of Asn-linked oligosaccharides on pituitary glycoprotein hormones: implications for biologic function (1986) (23)
Developmental changes in the modification of lysosomal enzymes in Dictyostelium discoideum. (1985) (23)
A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: molecular analysis of the chromosome 7 breakpoint. (2001) (23)
Variation at the DAOA / G 30 Locus Influences Susceptibility to Major Mood Episodes but Not Psychosis in Schizophrenia and Bipolar Disorder (2006) (23)
Refined Mapping of a Gene for Autosomal Dominant Progressive Sensorineural Hearing Loss (DFNA5) to a 2-cM Region, and Exclusion of a Candidate Gene That Is Expressed in the Cochlea (1997) (22)
Genome-wide association study identifies 30 loci associated with bipolar disorder (2019) (22)
Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples (2020) (22)
Isolation of yeast artificial chromosomes free of endogenous yeast chromosomes: construction of alternate hosts with defined karyotypic alterations. (1995) (21)
Localization of a novel t(1;7) translocation associated with Wilms' tumor predisposition and skeletal abnormalities (1996) (21)
The CMT2D locus: refined genetic position and construction of a bacterial clone-based physical map. (1999) (20)
Detection of potential GDF6 regulatory elements by multispecies sequence comparisons and identification of a skeletal joint enhancer. (2005) (20)
Dynamic evolution of V1R putative pheromone receptors between Mus musculus and Mus spretus (2009) (20)
Genotype–phenotype correlations in Darier disease: A focus on the neuropsychiatric phenotype (2018) (19)
A polymorphism within intron 11 of the tau gene is not increased in frequency in patients with sporadic Alzheimer's disease, nor does it influence the extent of tau pathology in the brain (2002) (19)
Mapping the RP10 locus for autosomal dominant retinitis pigmentosa on 7q: refined genetic positioning and localization within a well-defined YAC contig. (1996) (19)
Sulphation of proteins secreted by a human hepatoma-derived cell line. Sulphation of N-linked oligosaccharides on alpha 2HS-glycoprotein. (1986) (19)
Detecting highly conserved regions of the human genome by multispecies sequence comparisons. (2003) (19)
Report and abstracts of the First International Workshop on Human Chromosome 7 Mapping 1993. (1994) (19)
Reproduction and immunity-driven natural selection in the human WFDC locus. (2013) (18)
A YAC-based contig of 1.5 Mb spanning the human multidrug resistance gene region and delineating the amplification unit in three human multidrug-resistant cell lines. (1995) (18)
Clonal Diversity of Ig and T-cell Receptor Gene Rearrangements in Childhood B-Precursor Acute Lymphoblastic Leukaemia (2000) (18)
Human-mouse comparative mapping of the genomic region containing CDK6: localization of an evolutionary breakpoint (1999) (18)
High-resolution genomic mapping of the three human replication protein A genes (RPA1, RPA2, and RPA3). (1994) (18)
Clonal diversity of Ig and T-cell-receptor gene rearrangements identifies a subset of childhood B-precursor acute lymphoblastic leukemia with increased risk of relapse. (1998) (18)
Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorder (2010) (17)
Conversion events in gene clusters (2011) (17)
Novel human alpha1a-adrenoceptor single nucleotide polymorphisms alter receptor pharmacology and biological function. (2005) (17)
2006 expressed-sequence tags derived from human chromosome 7-enriched cDNA libraries. (1997) (16)
Comparative physical mapping of targeted regions of the rat genome (2001) (16)
Effort required to finish shotgun-generated genome sequences differs significantly among vertebrates (2010) (16)
Comparative analysis of the primate X-inactivation center region and reconstruction of the ancestral primate XIST locus. (2011) (16)
Lineage-specific evolution of the vertebrate Otopetrin gene family revealed by comparative genomic analyses (2011) (16)
Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours (2001) (16)
Detection of human apolipoprotein E3, E2, and E4 genotypes by an allele-specific oligonucleotide-primed polymerase chain reaction assay: development and validation. (1991) (15)
Birth-and-Death of KLK3 and KLK2 in Primates: Evolution Driven by Reproductive Biology (2012) (15)
Reply to Brunet and Doolittle: Both selected effect and causal role elements can influence human biology and disease (2014) (15)
An Effective Method for Detecting Gene Conversion Events in Whole Genomes (2010) (15)
Reconstructing the Evolutionary History of Complex Human Gene Clusters (2008) (15)
Human chromosome 7 circa 2004: a model for structural and functional studies of the human genome. (2004) (15)
Hormonal evaluation of female infertility and reproductive disorders. (1989) (14)
ComboScreen facilitates the multiplex hybridization-based screening of high-density clone arrays (2000) (14)
Functional expression of yeast artificial chromosome-human multidrug resistance genes in mouse cells. (1995) (14)
SHORT COMMUNICATION Fluorescence in Situ Hybridization of Y AC Clones after Alu-peR Amplification (1992) (14)
Formate-stimulated NaCl absorption in the proximal tubule is independent of the pendrin protein. (2002) (14)
Maintenance of hypomethylation status and preferential expression of exogenous humanMDR1/PGY1 gene in mouse L cells by YAC mediated transfer (1997) (14)
Methemoglobinemia from overdose of phenazopyridine hydrochloride. (1980) (13)
The PDS gene, Pendred syndrome and non-syndromic deafness DFNB4. (2000) (13)
Construction of a High-Resolution Physical Map of the ∼ 1-Mb Region of Human Chromosome 7q31.1-q31.2 Harboring a Putative Tumor Suppressor Gene (1999) (13)
Consortium, G.P A map of human genome variation from population-scale sequencing. Nature 467, 1061-1073 (2010) (13)
Alignment of Genomic DNA LAGAN and Multi-LAGAN : Efficient Tools for Large-Scale Multiple (2003) (13)
Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia (2006) (12)
Should all babies have their genome sequenced at birth? (2021) (12)
The end of the beginning: the race to begin human genome sequencing. (1996) (12)
The genomics workforce must become more diverse: a strategic imperative. (2021) (11)
In silico and functional studies of the regulation of the glucocerebrosidase gene. (2010) (11)
A Rare Myelin Protein Zero (MPZ) Variant Alters Enhancer Activity In Vitro and In Vivo (2010) (11)
Revealing Mammalian Evolutionary Relationships by Comparative Analysis of Gene Clusters (2012) (11)
Mutational analysis of two positional candidate susceptibility genes for bipolar disorder on chromosome 12q23‐q24: phenylalanine hydroxylase and human LIM‐homeobox LHX5 (2003) (11)
Brain-derived neurotrophic factor as a potential risk locus for bipolar disorder: Evidence, limitations, and implications (2004) (11)
National Human Genome Research Institute (NHGRI) Research Materials Available for Licensing (2009) (10)
Comparative analyses of the Dominant megacolon-SOX10 genomic interval in mouse and human (1999) (10)
An Examination of Single Nucleotide Polymorphism Selection Prioritization Strategies for Tests of Gene–Gene Interaction (2011) (10)
Realizing the Full Potential of Precision Medicine in Health and Health Care: A Vital Direction for Health and Health Care (2016) (10)
An effective approach for analyzing "prefinished" genomic sequence data. (1999) (9)
Organization of the gene encoding the human Kell blood group protein. (1995) (9)
Comparative sequence analysis of the Gdf6 locus reveals a duplicon-mediated chromosomal rearrangement in rodents and rapidly diverging coding and regulatory sequences. (2004) (9)
Localization of 67 exons on a YAC contig spanning 1.5 Mb around the multidrug resistance gene region of human chromosome 7q21.1. (1998) (9)
Poisoned legacy: environmental quality in the newly independent states (1993) (9)
Identification of candidate genes involved in coronary artery calcification by transcriptome sequencing of cell lines (2014) (9)
Construction of a high-resolution physical map of the approximate 1-Mb region of human chromosome 7q31.1-q31.2 harboring a putative tumor suppressor gene. (1999) (9)
Localization and characterization of the human ADP-ribosylation factor 5 (ARF5) gene. (1997) (8)
Erratum: Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder (2017) (8)
Detection of Hidden Intertextuality in the Scientific Publications (2012) (8)
Sequencing and Analyzing the t(1;7) Reciprocal Translocation Breakpoints Associated with a Case of Childhood-onset Schizophrenia/Autistic Disorder (2008) (8)
Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype [Corrigendum] (2010) (7)
Genomic Medicine Year in Review: 2019. (2019) (7)
Transient gene expression from yeast artificial chromosome DNA in mammalian cells is enhanced by adenovirus. (1997) (6)
Predictive and Precision Medicine with Genomic Data. (2019) (6)
A systematic association mapping on chromosome 6q in bipolar affective disorder—evidence for the melanin‐concentrating‐hormone‐receptor‐2 gene as a risk factor for bipolar affective disorder (2009) (6)
Evolutionary History Reconstruction for Mammalian Complex Gene Clusters (2009) (6)
Oligosaccharide Specificities of Phaseolus vulgaris (1987) (6)
Allele-specific oligonucleotide PCR. (2002) (6)
Molecular characterization of the mouse p47-phox (Ncf1) gene and comparative analysis of the mouse p47-phox (Ncf1) gene to the human NCF1 gene. (2000) (6)
Isolation of DNA from the centromere of human chromosome 7 by microdissection (1997) (5)
Physical mapping of the HOXA1 gene and the hnRPA2B1 gene in a YAC contig from human chromosome 7p14-p15 (1997) (5)
Restriction Fragment-Length Polymorphisms (1998) (4)
A p 47-phox Pseudogene Carries the Most Common Mutation Causing p 47-phox – deficient Chronic Granulomatous Disease (2013) (4)
Genetic and physical maps of jerker (Espn(je)) on mouse chromosome 4. (2002) (4)
Identification of 3'-terminal exons from yeast artificial chromosomes. (1995) (4)
Precision Health: Bringing Oral Health into the Context of Overall Health (2019) (4)
A scalable and flexible approach for investigating the genomic landscapes of phylogenetic incongruence. (2013) (4)
Progress in Positional Cloning of RP10 (7q31.3), RP1 (8q11–q21), and VMD1 (8q24) (1997) (3)
Inhibition of an anti‐Pr1d cold agglutinin by citrate present in commercial red cell preservative solutions (1990) (3)
Genomic Medicine Year in Review: 2020. (2020) (3)
Socialist Internationalism: Theoria and Praxis in Soviet International Law (1988) (3)
Sequence Diversity of Pan troglodytes Subspecies and the Impact of WFDC6 Selective Constraints in Reproductive Immunity (2013) (2)
Lessons of the Northern Ireland Peace Process (2005) (2)
Corrigendum: TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum (2011) (2)
21 – PCR-Based Screening of Yeast Artificial Chromosome Libraries (1995) (2)
Skin microbiome in health and disease (2010) (2)
CHAPTER 10 – Inter-Species Comparative Sequence Analysis: A Tool for Genomic Medicine (2009) (2)
Nicotinic acetylcholine receptor 7 subunit gene and attention deficit hyperactivity disorder. (2000) (1)
The Wellcome Trust Irlan/UK bipolar sibling pair study: Stage II analysis (2004) (1)
Opening plenary speaker: Human genomics, precision medicine, and advancing human health (2016) (1)
on the physical , cytogenetic , and genetic maps of chromosome 7 . The human obese ( OB ) gene : RNA expression pattern and mapping (2007) (1)
Author Correction: Pan-cancer analysis of whole genomes (2023) (1)
Abstract 13204: Acute Effects of a Small-Molecule Direct Myosin-Attenuator (MYK-581) in a Mini-Pig Genetic Model of Non-Obstructed Hypertrophic Cardiomyopathy: In Vivo Evidence for Contractile Regulation With Improved Compliance and Functional Reserve (2018) (1)
Examination of isoelectric focusing and electrophoretic methods for resolving acidic proteins (1986) (1)
Maurice Green - A pioneering virologist. (2018) (0)
Placemaking in Rosemount Parks (2015) (0)
Identification of candidate genes involved in coronary artery calcification by transcriptome sequencing of cell lines (2014) (0)
SYSTEMATIC SEQUENCING OF COMPLEX GENOMES (2001) (0)
Human Genomics a Decade after the Human Genome Project: Opportunities and Challenges (2014) (0)
A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources (2022) (0)
Genomics in 2K10: Fulfilling the Promise of a Sequenced Human Genome (2010) (0)
Peace Through Bloodshed: The Paradox of Hero. (2005) (0)
Mineralocorticoid-Induced Hypertension ) in Mouse Kidney : Role of Pendrin in Slc 26 a 4 ( PDS Deoxycorticosterone Upregulates (2003) (0)
Expression of the KIAA0319 gene from a haplotype associated with developmental dyslexia (2006) (0)
Polymorphisms in the glucocorticoid receptor gene and susceptibility to major affective disorders (2006) (0)
Cytogenetics in acute leukemia (2015) (0)
silico Reconstructing large regions of an ancestral mammalian genome in data (2004) (0)
Comparative genomics Beyond the human genome sequence (2001) (0)
Analyses of Mammalian Genomes Quantitative Estimates of Sequence Divergence for Comparative Material Supplemental (2003) (0)
TREML4 expression by myeloid cells may play a role in coronary artery disease (HUM1P.308) (2014) (0)
Gene Conversion of Sialic Acid Binding Domains in CD33-Related Siglecs by Adjacent Pseudogenes: A Novel Mechanism To Change Sialic Acid Binding Specificity. (2004) (0)
Contig Maps in Multiple Species Parallel Construction of Orthologous Sequence-Ready Clone (2002) (0)
Special Issue Editors’ Introduction: “Genomics and the Human Genome Project” (2018) (0)
Author Correction: Inferring structural variant cancer cell fraction (2022) (0)
Breakpoint Identification, Detection and Frequency of the 65-kb Deletion in the Cystinosis Gene, CTNS (1999) (0)
Positional cloning, association analysis, and expression studies provide convergent evidence that the cadherin gene fat contains a bipolar disorder susceptibility allele (2005) (0)
Author Correction: Patterns of somatic structural variation in human cancer genomes (2020) (0)
Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples (2020) (0)
Effect of formate on fluid absorption in proximal tubules of wild-type and knockout mice (2002) (0)
Use of sample sequencing to identify candidate genes in the cystinosis critical region of chromosome 17p13 • 618 (1997) (0)
Author Correction: The evolutionary history of 2,658 cancers (2023) (0)
Genome‐wide significant locus for Research Diagnostic Criteria Schizoaffective Disorder Bipolar type (2017) (0)
Erratum: Sequencing and analysis of 10,967 full-length cDNA clones from Xenopus laevis and Xenopus tropicalis reveals post-tetraploidization transcriptome remodeling (Genome Research (2006) 16, (796-803)) (2006) (0)
Annual review of genomics and human genetics (2000) (0)
Polymorphisms in the serotonin transporter, MAOA and COMT genes and susceptibility to unipolar depression (2004) (0)
Aligner Aligning Multiple Genomic Sequences With the Threaded Blockset data (2004) (0)
Further evidence that KIAA0319 is associated with developmental dyslexia (2006) (0)
Fish and CGH studies of gene rearrangement and amplification in drug resistance (1997) (0)
Opening plenary speaker: Human genomics, precision medicine, and advancing human health. (2016) (0)
Edinburgh Research Explorer Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia (2017) (0)
Bipolar disorder and polymorphisms in the dystobrevin binding protein gene (2004) (0)
Comparative sequencing of vertebrate genomes (2005) (0)
HealthBehaviorChange:CanGenomicsImprove BehavioralAdherence? (2012) (0)
Identification of autism susceptibility candidates on 7q (2000) (0)
Mutational analysis of 2 positional candidate susceptibility genes for bipolar disorder: PAH and LHX5 (2001) (0)
YEAR IN REVIEW Genomic Medicine Year in Review: 2020 (2020) (0)
Transcriptional regulatory sequence divergence between mouse and bat modifies forelimb length (2008) (0)
Gene Expression Profiles in Acute Myeloid Leukemias (AML): A Novel Approach Using SAGE and Custom Microarray. (2004) (0)
Regulatory divergence modifies limb length between mammals Material Supplemental (2008) (0)
Fulfilling the Promise of a Sequenced Human Genome – Part II (2009) (0)
Hormonal Evaluation of the Adult Woman : Reference Intervals (0)
Straight talk with... Eric Green. Interview by Erica Westly. (2010) (0)
Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder (2018) (0)
Erratum: Sequence diversity of pan troglodytes subspecies and the impact of WFDC6 selective constraints in reproductive immunity (Genome Biology and Evolution 5:12 (2512-2523) DOI: 10.1093/gbe/evt198) (2014) (0)
Biomedical research. The genome project: what will it do as a teenager? Interview by Jocelyn Kaiser. (2011) (0)
Abstracts of papers presented at the 1995 Meeting on Genome Mapping & Sequencing, May 10-May 14, 1995 (1991) (0)
Genomics—Past, Present, and Future: A Letter to My Daughter (2018) (0)
Supplementary Information : Recent selective pressure changes in human genes previously under balancing selection (2016) (0)
Detection of Human ApolipoproteinE 3 , E 2 , and E 4 Genotypes by an Allele-Specific Oligonucleotide-Primed Polymerase Chain Reaction Assay : Development and Validation (2004) (0)
Fluorescent in situ hybridization. (2002) (0)
Human genomics: A quarter century of progress (2015) (0)
Randomized Comparison of 3 Preventive Strategies Renal Insufficiency Following Contrast Media Administration Trial (REMEDIAL): A (2015) (0)
Sequencing and analysis of 10967 full-length cDNA clones from Xenopus laevis and Xenopus tropicalis (2005) (0)
HIGH-THROUGHPUT MUTATION ANALYSIS OF THE HUMAN AMINOACYL-tRNA SYNTHETASE GENES: IN SEARCH OF ADDITIONAL LOCI RESPONSIBLE FOR INHERITED PERIPHERAL NEUROPATHIES (2009) (0)
ps3) EN Route to the ERA of Genomic Medicine (2011) (0)
Letter to the Editor: The effects of hyperlipidaemia, hyperbilirubinaemia and haemolysis on tests performed by the Olympus AU 5000 multiple analyser (1989) (0)
Genomic Medicine Year in Review: 2022. (2022) (0)
Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (0)
disease in children in Kenya The consistent association between Epstein-Barr virus and Hodgkin's (2011) (0)
The Effect of Green Tea Extract on Endurance Performance in Young Adults (2010) (0)
genome by low-redundancy comparative sequencing An initial strategy for the systematic identification of functional elements in the human Mullikin (2005) (0)
Special Issue Editors’ Introduction: “Genomics and the Human Genome Project” (2018) (0)
U.S. helping to coordinate mine-clearing operation in Colombia (2017) (0)
Influencing the field. Interview by Kristie Nybo. (2011) (0)

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