Jean Weissenbach

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Jean Weissenbach is affiliated with the following schools: Paris-Saclay University, Université Paris Cité, University of Helsinki

Jean Weissenbach's AcademicInfluence.com Rankings

Jean Weissenbach

Biology

#1714

World Rank

#2791

Historical Rank

Genetics

#383

World Rank

#446

Historical Rank

biology Degrees

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Biology

Jean Weissenbach's Degrees

PhD Molecular Biology Université Paris Cité

Why Is Jean Weissenbach Influential?

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According to Wikipedia, Jean Weissenbach is a French biologist. He is the current director of the Genoscope. He is one of the pioneers of sequencing and genome analysis. Publications

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Jean Weissenbach'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

Initial sequencing and analysis of the human genome. (2001) (15222)
A human gut microbial gene catalogue established by metagenomic sequencing (2010) (9177)
The genome sequence of Drosophila melanogaster. (2000) (6125)
Enterotypes of the human gut microbiome (2011) (4920)
Identification and characterization of a spinal muscular atrophy-determining gene (1995) (3385)
The grapevine genome sequence suggests ancestral hexaploidization in major angiosperm phyla (2007) (3261)
A comprehensive genetic map of the human genome based on 5,264 microsatellites (1996) (3041)
Mutations in PCSK9 cause autosomal dominant hypercholesterolemia (2003) (2613)
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer (1993) (2347)
The Genome Sequence of the Malaria Mosquito Anopheles gambiae (2002) (2020)
The 1993–94 Généthon human genetic linkage map (1994) (1944)
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia (1996) (1938)
Genome duplication in the teleost fish Tetraodon nigroviridis reveals the early vertebrate proto-karyotype (2004) (1905)
A second-generation linkage map of the human genome (1992) (1791)
Structure and function of the global ocean microbiome (2015) (1716)
Genome evolution in yeasts (2004) (1583)
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene (1994) (1542)
The Phaeodactylum genome reveals the evolutionary history of diatom genomes (2008) (1451)
A candidate gene for familial Mediterranean fever (1997) (1401)
Nitrite-driven anaerobic methane oxidation by oxygenic bacteria (2010) (1396)
Eukaryotic plankton diversity in the sunlit ocean (2015) (1309)
The Medicago Genome Provides Insight into the Evolution of Rhizobial Symbioses (2011) (1131)
The complete genome sequence of the lactic acid bacterium Lactococcus lactis ssp. lactis IL1403. (2001) (1104)
A Gene Map of the Human Genome (1996) (1080)
Mapping of a susceptibility locus for Crohn's disease on chromosome 16 (1996) (1046)
Deciphering the evolution and metabolism of an anammox bacterium from a community genome (2006) (1044)
Genome sequence of the metazoan plant-parasitic nematode Meloidogyne incognita (2008) (1014)
Genome sequence and gene compaction of the eukaryote parasite Encephalitozoon cuniculi (2001) (1003)
The banana (Musa acuminata) genome and the evolution of monocotyledonous plants (2012) (927)
Genome sequence of the plant pathogen Ralstonia solanacearum (2002) (896)
An STS-Based Map of the Human Genome (1995) (818)
Global trends of whole-genome duplications revealed by the ciliate Paramecium tetraurelia (2006) (787)
Comparative Genomics of Multidrug Resistance in Acinetobacter baumannii (2006) (765)
Enterotypes of the human gut microbiome (2011) (713)
Towards the definition of a core of microorganisms involved in anaerobic digestion of sludge (2009) (710)
A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex (1996) (681)
Determinants of community structure in the global plankton interactome (2015) (672)
A physical map of 30,000 human genes. (1998) (670)
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules (1991) (663)
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients (1997) (634)
A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family (1997) (615)
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia (1999) (601)
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12 (1993) (568)
Plankton networks driving carbon export in the oligotrophic ocean (2015) (532)
New susceptibility locus for rheumatoid arthritis suggested by a genome-wide linkage study. (1998) (524)
A radiation hybrid map of the human genome. (1996) (467)
Genome sequence of the cyanobacterium Prochlorococcus marinus SS120, a nearly minimal oxyphototrophic genome (2003) (465)
Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy (1995) (460)
Effector diversification within compartments of the Leptosphaeria maculans genome affected by Repeat-Induced Point mutations (2011) (457)
Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome. (2001) (453)
Cardiac myosin binding protein–C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy (1995) (453)
A first-generation physical map of the human genome (1993) (436)
Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus (1992) (434)
Mechanisms of Evolution in Rickettsia conorii and R. prowazekii (2001) (421)
Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome llq (1994) (407)
The complete genome sequence of Lactobacillus bulgaricus reveals extensive and ongoing reductive evolution. (2006) (405)
The Xist RNA Gene Evolved in Eutherians by Pseudogenization of a Protein-Coding Gene (2006) (398)
A method for constructing radiation hybrid maps of whole genomes (1994) (385)
An international two–stage genome–wide search for schizophrenia susceptibility genes (1995) (382)
Molecular Basis of Evolutionary Events That Shaped the Hardness Locus in Diploid and Polyploid Wheat Species (Triticum and Aegilops)w⃞ (2005) (379)
A gene for familial hemiplegic migraine maps to chromosome 19 (1993) (377)
Continuum of overlapping clones spanning the entire human chromosome 21q (1992) (376)
A Holistic Approach to Marine Eco-Systems Biology (2011) (365)
A deletion map of the human Y chromosome based on DNA hybridization. (1986) (360)
Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus (1992) (355)
Unique features revealed by the genome sequence of Acinetobacter sp. ADP1, a versatile and naturally transformation competent bacterium. (2004) (354)
Genetic localization of a locus controlling the intensity of infection by Schistosoma mansoni on chromosome 5q31–q33 (1996) (342)
Genomic evidence for ameiotic evolution in the bdelloid rotifer Adineta vaga (2013) (333)
Estimate of human gene number provided by genome-wide analysis using Tetraodon nigroviridis DNA sequence (2000) (331)
Comparative Analysis of Acinetobacters: Three Genomes for Three Lifestyles (2008) (322)
Two interferon mRNAs in human fibroblasts: in vitro translation and Escherichia coli cloning studies. (1980) (321)
A calcium channel mutation causing hypokalemic periodic paralysis. (1994) (312)
Open science resources for the discovery and analysis of Tara Oceans data (2015) (305)
The genome sequence of the model ascomycete fungus Podospora anserina (2008) (301)
“Candidatus Cloacamonas Acidaminovorans”: Genome Sequence Reconstruction Provides a First Glimpse of a New Bacterial Division (2008) (301)
Novel predominant archaeal and bacterial groups revealed by molecular analysis of an anaerobic sludge digester. (2005) (300)
Hox cluster disintegration with persistent anteroposterior order of expression in Oikopleura dioica (2004) (299)
Genome structure and metabolic features in the red seaweed Chondrus crispus shed light on evolution of the Archaeplastida (2013) (299)
Mutant WD-repeat protein in triple-A syndrome (2000) (287)
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia. (2000) (283)
A complete collection of single-gene deletion mutants of Acinetobacter baylyi ADP1 (2008) (282)
A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomes (1986) (282)
A non–syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q (1994) (277)
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2. (2003) (272)
Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia) (2000) (267)
Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23 (1996) (256)
The human obese (OB) gene: RNA expression pattern and mapping on the physical, cytogenetic, and genetic maps of chromosome 7. (1995) (255)
Plasticity of Animal Genome Architecture Unmasked by Rapid Evolution of a Pelagic Tunicate (2010) (254)
Vector integration is nonrandom and clustered and influences the fate of lymphopoiesis in SCID-X1 gene therapy. (2007) (253)
Loss of the chromosomal region 10q23-25 in prostate cancer. (1995) (248)
Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1. (2002) (247)
An autosomal locus predisposing to deletions of mitochondrial DNA (1995) (245)
Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome. (2003) (245)
Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22. (1994) (244)
Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF). (1998) (240)
Complete genome sequence of the entomopathogenic and metabolically versatile soil bacterium Pseudomonas entomophila (2006) (238)
Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy. (1995) (234)
Molecular approach to thermogenesis in brown adipose tissue: cDNA cloning of the mitochondrial uncoupling protein. (1985) (229)
Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31–32 in three European families (1994) (225)
Genomic Exploration of the Hemiascomycetous Yeasts: 1. A set of yeast species for molecular evolution studies 1 (2000) (222)
Comparative genomics of protoploid Saccharomycetaceae. (2009) (221)
Genome-wide search for linkage of bipolar affective disorders in a very large pedigree derived from a homogeneous population in quebec points to a locus of major effect on chromosome 12q23-q24. (1999) (216)
Vertebrate-Type Intron-Rich Genes in the Marine Annelid Platynereis dumerilii (2005) (213)
Methylobacterium Genome Sequences: A Reference Blueprint to Investigate Microbial Metabolism of C1 Compounds from Natural and Industrial Sources (2009) (212)
Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development (2005) (212)
Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1. (1997) (206)
Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8. (2001) (205)
A Tale of Two Oxidation States: Bacterial Colonization of Arsenic-Rich Environments (2007) (201)
Complete cDNA-derived amino acid sequence of rat brown fat uncoupling protein. (1986) (200)
Genomic Encyclopedia of Bacteria and Archaea: Sequencing a Myriad of Type Strains (2014) (195)
An integrated analysis of the genome of the hyperthermophilic archaeon Pyrococcus abyssi (2003) (187)
Mutations in the gene encoding SLURP-1 in Mal de Meleda. (2001) (185)
Pseudoautosomal DNA sequences in the pairing region of the human sex chromosomes (1985) (184)
A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10 (1993) (183)
Anaerobic ammonium oxidation by marine and freshwater planctomycete-like bacteria (2003) (182)
Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas. (1996) (178)
Human XX males with Y single-copy DNA fragments (1984) (175)
A panoramic view of gene expression in the human kidney (2003) (174)
Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11 (1993) (173)
A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish (1996) (172)
A placenta-specific receptor for the fusogenic, endogenous retrovirus-derived, human syncytin-2 (2008) (169)
A second locus for Marfan syndrome maps to chromosome 3p24.2–p25 (1994) (167)
A radiation hybrid map of 506 STS markers spanning human chromosome 11 (1994) (163)
Extending the Bacillus cereus group genomics to putative food-borne pathogens of different toxicity. (2008) (162)
The sequence of rice chromosomes 11 and 12, rich in disease resistance genes and recent gene duplications (2005) (160)
A human Y-linked DNA polymorphism and its potential for estimating genetic and evolutionary distance. (1985) (157)
Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q (1993) (156)
The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1 (1995) (156)
Metabolic diversity among main microorganisms inside an arsenic-rich ecosystem revealed by meta- and proteo-genomics (2011) (154)
DNA replication origin interference increases the spacing between initiation events in human cells. (2006) (145)
Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians. (1996) (144)
A novel gene that encodes a protein with a putative src homology 3 domain is a candidate gene for familial juvenile nephronophthisis. (1997) (143)
Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19. (1994) (140)
Characterization and repeat analysis of the compact genome of the freshwater pufferfish Tetraodon nigroviridis. (2000) (140)
Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14 (1995) (140)
Clostridium sticklandii, a specialist in amino acid degradation:revisiting its metabolism through its genome sequence (2010) (139)
A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene. (1994) (139)
A sex chromosome rearrangement in a human XX male caused by Alu—Alu recombination (1987) (138)
A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q. (1995) (133)
Molecular Evidence for Novel Planctomycete Diversity in a Municipal Wastewater Treatment Plant (2003) (128)
Novel Major Bacterial Candidate Division within a Municipal Anaerobic Sludge Digester (2005) (125)
A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21. (1997) (124)
The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac α and β myosin heavy chain genes on chromosome 14q11.2−q13 (1995) (123)
A common gene for juvenile and adult-onset primary open-angle glaucomas confined on chromosome 1q. (1995) (122)
A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2p (1993) (121)
A gene for achondroplasia–hypochondroplasia maps to chromosome 4p (1994) (120)
Notch3 Mutations in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL), a Mendelian Condition Causing Stroke and Vascular Dementia (1997) (120)
Fish genomics and biology. (2005) (119)
A DNA probe detecting multiple haplotypes of the human Y chromosome. (1986) (118)
An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p. (1996) (118)
Physical mapping of the human pseudo‐autosomal region; comparison with genetic linkage map. (1988) (117)
Structure, Function, and Evolution of the Thiomonas spp. Genome (2010) (116)
Identification of three distinct regions of allelic deletions on the short arm of chromosome 8 in hepatocellular carcinoma (1999) (115)
Sequence and analysis of chromosome 3 of the plant Arabidopsis thaliana. (2000) (114)
A genetic linkage map of human chromosome 20 composed entirely of microsatellite markers. (1992) (113)
Characterization of the NPHP1 locus: mutational mechanism involved in deletions in familial juvenile nephronophthisis. (2000) (112)
Random search for shared chromosomal regions in four affected individuals: the assignment of a new hereditary ataxia locus. (1995) (111)
The beta2‐microglobulin mRNA in human Daudi cells has a mutated initiation codon but is still inducible by interferon. (1983) (111)
Localization of a gene causing cystinuria to chromosome 2p (1994) (111)
Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors. (2000) (110)
Loss of heterozygosity in sporadic breast tumours at the BRCA2 locus on chromosome 13q12-q13. (1995) (110)
The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21–q24 (1995) (110)
The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16. (1996) (110)
Clinical and genetic heterogeneity of hypochondroplasia. (1996) (107)
Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer families. (1994) (106)
Erratum: Initial sequencing and analysis of the human genome: International Human Genome Sequencing Consortium (Nature (2001) 409 (860-921)) (2001) (106)
An abnormal terminal X-Y interchange accounts for most but not all cases of human XX maleness (1987) (105)
Age and origin of two common MLH1 mutations predisposing to hereditary colon cancer. (1996) (105)
Chromosome Y-specific DNA in related human XX males (1985) (104)
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis (2011) (104)
Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat. (1996) (101)
The gene for triphalangeal thumb maps to the subtelomeric region of chromosome 7q (1994) (101)
Chaetognath phylogenomics: a protostome with deuterostome-like development (2006) (98)
Chromosome 9p deletions in cutaneous malignant melanoma tumors: the minimal deleted region involves markers outside the p16 (CDKN2) gene. (1995) (98)
Pichia sorbitophila, an Interspecies Yeast Hybrid, Reveals Early Steps of Genome Resolution After Polyploidization (2012) (98)
Erratum: Enterotypes of the human gut microbiome (Nature (2011) 473 (174-180)) (2011) (97)
A physical map of human chromosome 7: an integrated YAC contig map with average STS spacing of 79 kb. (1997) (94)
Evidence of a non-MHC susceptibility locus in type I diabetes linked to HLA on chromosome 6. (1997) (94)
Digital expression profiling of novel diatom transcripts provides insight into their biological functions (2010) (93)
A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34. (2000) (92)
Human peroxisome proliferator-activated receptor-gamma2: genetic mapping, identification of a variant in the coding sequence, and exclusion as the gene responsible for lipoatrophic diabetes. (1998) (91)
Single-copy DNA sequences specific for the human Y chromosome (1983) (90)
Substitution of a conserved cysteine-996 in a cysteine-rich motif of the laminin alpha2-chain in congenital muscular dystrophy with partial deficiency of the protein. (1996) (88)
Genetic and physical mapping of the Chediak-Higashi syndrome on chromosome 1q42-43. (1996) (88)
Improved PCR-walking for large-scale isolation of plant T-DNA borders. (2001) (88)
The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8. (1994) (88)
Whole genome sequence comparisons and "full-length" cDNA sequences: a combined approach to evaluate and improve Arabidopsis genome annotation. (2004) (88)
Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11. (1999) (88)
Revealing the hidden functional diversity of an enzyme family. (2014) (86)
High-density genetic map of the BRCA1 region of chromosome 17q12-q21. (1993) (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)
An interspersed repeated sequence specific for human subtelomeric regions. (1990) (85)
Iterative reconstruction of a global metabolic model of Acinetobacter baylyi ADP1 using high-throughput growth phenotype and gene essentiality data (2008) (84)
Mapping of a second locus for lamellar ichthyosis to chromosome 2q33-35. (1996) (84)
The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q. (1996) (83)
Rapid increase of mitochondrial uncoupling protein and its mRNA in stimulated brown adipose tissue (1984) (83)
Linkage between atopy and the IgE high-affinity receptor gene at 11q13 in atopic dermatitis families (1998) (83)
Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12. (1993) (83)
Linkage of the gene for cystinosis to markers on the short arm of chromosome 17 (1995) (83)
A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23. (1996) (83)
Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22. (1996) (82)
Remarkable compartmentalization of transposable elements and pseudogenes in the heterochromatin of the Tetraodon nigroviridis genome (2002) (80)
Two new loci for autosomal recessive ichthyosis on chromosomes 3p21 and 19p12-q12 and evidence for further genetic heterogeneity. (2000) (79)
Genomic Exploration of the Hemiascomycetous Yeasts: 18. Comparative analysis of chromosome maps and synteny with Saccharomyces cerevisiae (2000) (78)
Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis (1994) (76)
The DNA sequence and analysis of human chromosome 14 (2003) (76)
An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3. (1995) (76)
Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2. (1996) (75)
A 94 kb genomic sequence 3' to the murine Xist gene reveals an AT rich region containing a new testis specific gene Tsx. (1996) (74)
Extensive sequence homologies between Y and other human chromosomes. (1984) (73)
A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13. (1995) (71)
Effect of Threonylcarbamoyl Modification (t6A) in Yeast tRNAArgIII on Codon‐Anticodon and Anticodon‐Anticodon Interactions (1981) (71)
Genetic Mapping in the Xp11.2 Region of a New Form of X-Linked Hypophosphatemic Rickets (1993) (70)
Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p. (1998) (67)
Mapping of Papillon-Lefèvre Syndrome to the Chromosome 11q14 Region (1997) (67)
Functional Diversity of Carbohydrate-Active Enzymes Enabling a Bacterium to Ferment Plant Biomass (2014) (67)
Exchange of terminal portions of X- and Y-chromosomal short arms in human XY females. (1989) (67)
Identification of the Anopheles gambiae ATP-binding cassette transporter superfamily genes. (2003) (67)
Remodelling of the homeobox gene complement in the tunicate Oikopleura dioica (2005) (66)
Loss of heterozygosity in the chromosomal region 12p12-13 is very common in childhood acute lymphoblastic leukemia and permits the precise localization of a tumor-suppressor gene distinct from p27KIP1. (1995) (65)
Karyotype and chromosome location of characteristic tandem repeats in the pufferfish Tetraodon nigroviridis (2000) (65)
The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus. (1996) (65)
Human Hormone-Sensitive Lipase: Genetic Mapping, Identification of a New Dinucleotide Repeat, and Association With Obesity and NIDDM (1998) (65)
Human genome anatomy: BACs integrating the genetic and cytogenetic maps for bridging genome and biomedicine. (1999) (64)
Yeast tRNALeu (Anticodon U‐A‐G) translates all six leucine codons in extracts from interferon treated cells (1977) (64)
An isolated cardiac conduction disease maps to chromosome 19q. (1995) (63)
A gene for Leber's congenital amaurosis maps to chromosome 17p (1995) (62)
Allelic imbalance on chromosome I in human breast cancer. II. Microsatellite repeat analysis (1995) (61)
Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity. (1995) (61)
Identification of the Last Unknown Genes in the Fermentation Pathway of Lysine* (2007) (61)
Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22. (1995) (60)
Nitrilase Activity Screening on Structurally Diverse Substrates: Providing Biocatalytic Tools for Organic Synthesis (2013) (60)
Human desmin gene: cDNA sequence, regional localization and exclusion of the locus in a familial desmin-related myopathy (1996) (59)
Long-range restriction map of the terminal part of the short arm of the human X chromosome. (1990) (58)
Conservation of the T-Cell Receptor α/δ Linkage in the Teleost Fish Tetraodon nigroviridis (2002) (58)
Atlas of gene expression in the mouse kidney: new features of glomerular parietal cells. (2011) (57)
Genomic Exploration of the Hemiascomycetous Yeasts: 20. Evolution of gene redundancy compared to Saccharomyces cerevisiae (2000) (57)
Localization of the Schwartz-Jampel syndrome (SJS) locus to chromosome 1p34-p36.1 by homozygosity mapping. (1995) (56)
Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families. (1995) (56)
Community‐Level Responses to Iron Availability in Open Ocean Plankton Ecosystems (2019) (56)
Genomic Exploration of the Hemiascomycetous Yeasts: 19. Ascomycetes‐specific genes (2000) (56)
Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2p. (1996) (56)
Two highly polymorphic minisatellites from the pseudoautosomal region of the human sex chromosomes. (1987) (55)
Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A (2004) (54)
Global heterochromatic colocalization of transposable elements with minisatellites in the compact genome of the pufferfish Tetraodon nigroviridis. (2004) (54)
Acinetobacter baylyi ADP1 as a model for metabolic system biology. (2009) (52)
A second generation linkage map of the human genome based on highly informative microsatellite loci. (1993) (52)
Complete Genome Sequence of Streptomyces cattleya NRRL 8057, a Producer of Antibiotics and Fluorometabolites (2011) (52)
Highly homologous loci on the X and Y chromosomes are hot–spots for ectopic recombinations leading to XX maleness (1994) (51)
A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites. (1993) (51)
Close mapping of the focal non-epidermolytic palmoplantar keratoderma (PPK) locus associated with oesophageal cancer (TOC). (1996) (51)
Genetic linkage of Meleda disease to chromosome 8qter (1998) (51)
A gene for Holt–Oram syndrome maps to the distal long arm of chromosome 12 (1994) (51)
Microsatellite polymorphisms and the genetic linkage map of the human genome. (1993) (51)
Extensive DNA sequence homologies between the human Y and the long arm of the X chromosome. (1985) (51)
The pseudoautosomal region of the human sex chromosomes. (1986) (50)
An active non-LTR retrotransposon with tandem structure in the compact genome of the pufferfish Tetraodon nigroviridis. (2003) (50)
Correlations of allelic imbalance of chromosome 14 with adverse prognostic parameters in 148 renal cell carcinomas (1996) (49)
Analysis of major repetitive DNA sequences in the dog (Canis familiaris) genome (1999) (47)
Use of genetic and physical mapping to locate the spinal muscular atrophy locus between two new highly polymorphic DNA markers. (1994) (47)
Autosomal recessive lamellar ichthyosis: identification of a new mutation in transglutaminase 1 and evidence for genetic heterogeneity. (1995) (46)
Lipoxygenase-3 ( ALOXE 3 ) and 12 ( R )-lipoxygenase ( ALOX 12 B ) are mutated in non-bullous congenital ichthyosiform erythroderma ( NCIE ) linked to chromosome 17 p 13 . 1 (2001) (46)
Genomic Exploration of the Hemiascomycetous Yeasts: 2. Data generation and processing (2000) (46)
The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac alpha and beta myosin heavy chain genes on chromosome 14q11.2-q13. (1995) (45)
The primary structure of rabbit liver tRNAPhe and its comparison with known tRNAPhe sequences (1973) (45)
A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36 (1998) (45)
Refinement of the OPA1 gene locus on chromosome 3q28-q29 to a region of 2-8 cM, in one Cuban pedigree with autosomal dominant optic atrophy type Kjer. (1995) (44)
Pairing properties of the methylester of 5-carboxymethyl uridine in the wobble position of yeast tRNA3Arg. (1978) (44)
Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q. (1996) (44)
The Sjögren-Larsson Syndrome gene is close to D17S805 as determined by linkage analysis and allelic association (1994) (44)
Microbial Degradation of a Recalcitrant Pesticide: Chlordecone (2016) (43)
Positional candidate genes for congenital chloride diarrhea suggested by high-resolution physical mapping in chromosome region 7q31. (1996) (43)
Autosomal recessive lamellar ichthyosis: identification of a new mutation in transglutaminase 1 and evidence for genetic heterogeneity (1995) (43)
Proteome Adaptation to High Temperatures in the Ectothermic Hydrothermal Vent Pompeii Worm (2012) (42)
Refining the localization of the PKD2 locus on chromosome 4q by linkage analysis in Spanish families with autosomal dominant polycystic kidney disease type 2. (1995) (42)
Insights into metazoan evolution from alvinella pompejana cDNAs (2010) (42)
Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies (1994) (41)
Confirmation of genetic heterogeneity in familial psoriasis. (1995) (41)
Synthesis of Mono‐ and Dihydroxylated Amino Acids with New α‐Ketoglutarate‐Dependent Dioxygenases: Biocatalytic Oxidation of CH Bonds (2014) (40)
Report of the First International Workshop on Human Chromosome 20 Mapping 1993. (1994) (40)
Confinement of PGL, an Imprinted Gene Causing Hereditary Paragangliomas, to a 2-cM Interval on 11q22–q23 and Exclusion of DRD2 and NCAM as Candidate Genes (1996) (40)
Report of the committee on the genetic constitution of the Y chromosome. (1988) (40)
The CEPH consortium linkage map of human chromosome 16. (1994) (38)
Annotation of microsporidian genomes using transcriptional signals (2012) (38)
Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome gene. (1994) (38)
Refined genetic mapping of X-linked thoracoabdominal syndrome. (1996) (37)
A fourth locus for autosomal dominant hypercholesterolemia maps at 16q22.1 (2010) (37)
Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anemia group C in a 2.6-cM interval and contributes to the fine map of 9q22.3. (1994) (37)
A Conserved Gene Cluster Rules Anaerobic Oxidative Degradation of l-Ornithine (2009) (37)
Survey of CAG/CTG repeats in human cDNAs representing new genes: candidates for inherited neurological disorders. (1996) (36)
The genetic locus for free sialic acid storage disease maps to the long arm of chromosome 6. (1994) (36)
Refined mapping of a gene (NPH1) causing familial juvenile nephronophthisis and evidence for genetic heterogeneity. (1994) (36)
Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy. (1997) (36)
A locus for Fanconi anemia on 16q determined by homozygosity mapping. (1996) (36)
No evidence of genetic heterogeneity in dominant optic atrophy. (1995) (35)
Effect of threonylcarbamoyl modification (t6A) in yeast tRNA Arg III on codon-anticodon and anticodon-anticodon interactions. A thermodynamic and kinetic evaluation. (1981) (35)
Genetic heterogeneity of Usher syndrome type 1 in French families. (1994) (35)
Sequence and analysis of chromosome I of the amitochondriate intracellular parasite Encephalitozoon cuniculi (Microspora). (2001) (35)
The Cyst-Dividing Bacterium Ramlibacter tataouinensis TTB310 Genome Reveals a Well-Stocked Toolbox for Adaptation to a Desert Environment (2011) (35)
Presence of the methylester of 5-carboxymethyl uridine in the wobble position of the anticodon of tRNAIII Arg from brewer's yeast. (1975) (35)
A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21 (2007) (34)
Molecular Analyses of the Microbial Community Composition of an Anoxic Basin of a Municipal Wastewater Treatment Plant Reveal a Novel Lineage of Proteobacteria (2010) (34)
Prediction and identification of sequences coding for orphan enzymes using genomic and metagenomic neighbours (2012) (33)
Selective intestinal malabsorption of vitamin B12 displays recessive mendelian inheritance: assignment of a locus to chromosome 10 by linkage. (1995) (33)
Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian families. (1993) (33)
The role of SOX9 in autosomal sex reversal and campomelic dysplasia. (1995) (33)
The human metagenome: our other genome? (2011) (33)
European Gene Mapping Project (EUROGEM): Genetic Maps based on the CEPH reference families (1994) (32)
Lamellar Ichthyosis: further narrowing, physical and expression mapping of the chromosome 2 candidate locus (1998) (32)
Evidence for locus heterogeneity in acrocephalosyndactyly: a refined localization for the Saethre-Chotzen syndrome locus on distal chromosome 7p--and exclusion of Jackson-Weiss syndrome from craniosynostosis loci on 7p and 5q. (1994) (32)
Genomic Exploration of the Hemiascomycetous Yeasts: 21. Comparative functional classification of genes (2000) (31)
Genetic exclusion of 14 candidate genes in lipoatropic diabetes using linkage analysis in 10 consanguineous families. (1997) (31)
A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C). (1995) (31)
The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2. (1995) (31)
Identification of the translation products of human fibroblast interferon mRNA in reticulocyte lysates. (1979) (31)
Genetic and physical characterization of the early-onset Alzheimer's disease AD3 locus on chromosome 14q24.3. (1995) (31)
Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellites. (1994) (30)
Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM interval (1996) (30)
Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysis. (1995) (30)
Fine structure mapping of the human X-linked hypophosphatemic rickets gene locus. (1994) (30)
Genetic linkage analysis in hereditary non-polyposis colon cancer syndrome. (1995) (30)
Fine mapping of Best's macular dystrophy localizes the gene in close proximity to but distinct from the D11S480/ROM1 loci. (1994) (30)
A second-generation YAC contig map of human chromosome 3. (1995) (30)
Regulation of human gamma-interferon and beta-interferon gene expression in PHA-activated lymphocytes. (1986) (30)
A Synthetic Alternative to Canonical One-Carbon Metabolism. (2017) (29)
The gene for X-linked hypophosphataemic rickets maps to a 200–300 kb region in Xp22.1, and is located on a single YAC containing a putative vitamin D response element (VDRE) (1996) (29)
The sequences of nucleotides in tRNAArg III from brewer's yeast (1972) (29)
Four-hundred million years of conserved synteny of human Xp and Xq genes on three Tetraodon chromosomes. (2002) (29)
Mapping of Microsatellite Markers in the Alagille Region and Screening of Microdeletions by Genotyping 23 Patients (1994) (29)
Discovery and characterization of a new bacterial candidate division by an anaerobic sludge digester metagenomic approach (2008) (29)
The gene for Darier's disease maps between D12S78 and D12S79. (1994) (29)
An Xp22.1–p22.2 YAC Contig Encompassing the Disease Loci for RS, KFSD, CLS, HYP and RP15: Refined Localization of RS (1996) (28)
Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12 (1996) (28)
Characterization of the genomic organization of the region bordering the centromere of chromosome V of Podospora anserina by direct sequencing. (2003) (28)
Addendum: Enterotypes of the human gut microbiome (2014) (28)
Lysosomal free sialic acid storage disorders with different phenotypic presentations--infantile-form sialic acid storage disease and Salla disease--represent allelic disorders on 6q14-15. (1995) (28)
Machado-Joseph disease in four Chinese pedigrees (1997) (27)
A linkage study of the N-methyl-D-aspartate receptor subunit gene loci and schizophrenia in southern African Bantu-speaking families. (1996) (27)
Linkage disequilibrium utilized to establish a refined genetic position of the Salla disease locus on 6q14-q15. (1995) (27)
Non-specific X-linked mental retardation: linkage analysis in MRX2 and MRX4 families revisited. (1994) (27)
Synthesis of human interferon beta 1 in Escherichia coli infected by a lambda phage recombinant containing a human genomic fragment. (1981) (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)
A linkage study of the N‐methyl‐D‐aspartate receptor subunit gene loci and schizophrenia in southern African Bantu‐speaking families (1997) (26)
A subtracted cDNA library from the zebrafish (Danio rerio) embryonic inner ear. (2002) (26)
A dinucleotide repeat polymorphism at the Kallmann locus (Xp22.3). (1991) (26)
Linkage analysis of candidate myelin genes in familial multiple sclerosis (1999) (25)
Localization and expression analysis of a novel conserved brain expressed transcript, Brx/BRX, lying within the Xic/XIC candidate region (1997) (24)
Expressed sequence tags from the phytopathogenic fungus Botrytis cinerea (2005) (24)
Microsatellite-based fine mapping of the Van der Woude syndrome locus to an interval of 4.1 cM between D1S245 and D1S414. (1995) (24)
Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13 (1996) (24)
YAC/STS map across 12 Mb of Xq27 at 25-kb resolution, merging Xq26-qter. (1996) (24)
A 45,X male with a Yp/18 translocation (1986) (24)
Association of rheumatoid arthritis with an amino acid allelic variation of the T cell receptor. (1997) (24)
Haplotype analysis in gelsoiin‐related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and Japan (1995) (24)
Fine mapping of the cystinosis gene using an integrated genetic and physical map of a region within human chromosome band 17p13. (1996) (24)
The CEPH consortium linkage map of human chromosome 11. (1995) (23)
Pilot Anopheles gambiae full-length cDNA study: sequencing and initial characterization of 35,575 clones (2005) (23)
Identification and cloning in yeast artificial chromosomes of a region of elevated loss of heterozygosity on chromosome 1p31.1 in human breast cancer. (1995) (23)
Natural Chlordecone Degradation Revealed by Numerous Transformation Products Characterized in Key French West Indies Environmental Compartments. (2019) (23)
Parallel evolution of non-homologous isofunctional enzymes in methionine biosynthesis. (2017) (23)
A new family linked to the RP13 locus for autosomal dominant retinitis pigmentosa on distal 17p. (1996) (23)
The spinocerebellar ataxia 2 locus is located within a 3-cM interval on chromosome 12q23-24.1. (1995) (22)
Fine localization of the locus for autosomal dominant retinitis pigmentosa on chromosome 17p. (1995) (22)
The inhibition of translation of synthetic polyribonucleotides and mengo RNA in extracts from interferon-treated L cells and its reversion by yeast tRNAs. (1976) (22)
Homology between a 173-kb region from mouse chromosome 10, telomeric to the Ifng locus, and human chromosome 12q15. (2001) (22)
Conservation of human-derived pseudoautosomal sequences on the sex chromosomes of the great apes. (1987) (22)
A radiation hybrid transcript map of the mouse genome (2001) (22)
A physical map of human chromosome 14 (2001) (22)
Construction of a YAC contig and a STS map spanning at least seven megabasepairs in chromosome 5q34-35. (1994) (22)
Exclusion of HRAS from long QT locus (1994) (22)
The Human Genome Project: From Mapping to Sequencing (1998) (21)
Yeast artificial chromosome and radiation hybrid map of loci in chromosome band 8p22, a common region of allelic loss in multiple human cancers. (1994) (21)
Absence of Y-specific DNA sequences in human 46,XX true hermaphrodites and in 45,X mixed gonadal dysgenesis (1987) (21)
Rapid and early determination of sex using trophoblast biopsy specimens and Y chromosome specific DNA probes. (1984) (21)
A 1.8-Mb YAC contig in Xp11.23: identification of CpG islands and physical mapping of CA repeats in a region of high gene density. (1994) (21)
Isolation of sequences from Xp22.3 and deletion mapping using sex chromosome rearrangements from human X-Y interchange sex reversals. (1990) (21)
Exploring nervous system transcriptomes during embryogenesis and metamorphosis in Xenopus tropicalis using EST analysis (2007) (21)
Novel metabolic features in Acinetobacter baylyi ADP1 revealed by a multiomics approach (2014) (20)
Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP) (1994) (20)
Strong linkage disequilibrium and haplotype analysis in Japanese pedigrees with Machado-Joseph disease. (1996) (19)
Conservation of the T-cell receptor alpha/delta linkage in the teleost fish Tetraodon nigroviridis. (2002) (19)
Ring Y chromosome: molecular characterization by DNA probes. (1991) (19)
The gene S promoter of hepatitis B virus confers constitutive gene expression (1983) (19)
YAC/STS map of 9 Mb of Xq26 at 100-kb resolution, localizing 6 ESTs, 6 genes, and 32 genetic markers. (1996) (19)
Genetic linkage of progressive pseudorheumatoid dysplasia to a 3-cM interval of chromosome 6q22 (1998) (19)
Numerous novel annotations of the human genome sequence supported by a 5'-end-enriched cDNA collection. (2004) (18)
A YAC contig spanning the dominant retinitis pigmentosa locus (RP9) on chromosome 7p. (1995) (18)
Normal and abnormal interchanges between the human X and Y chromosomes. (1987) (18)
Human genetic map. Genome maps V. Wall chart. (1994) (18)
Linkage disequilibrium mapping of the cornea plana congenita gene CNA2. (1995) (18)
Cell complementation using Genebridge 4 human:rodent hybrids for physical mapping of novel mitochondrial respiratory chain deficiency genes. (2002) (18)
16S rRNA and As-Related Functional Diversity: Contrasting Fingerprints in Arsenic-Rich Sediments from an Acid Mine Drainage (2015) (17)
Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q. (1998) (17)
Aicardi–Goutières syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease? (1999) (17)
The gene for Machado–Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14q (1994) (17)
The rise of genomics. (2016) (17)
A high-density microsatellite map of the ataxia-telangiectasia locus (1995) (17)
The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of ∼3 cM on chromosome 14q24.3-q32.2 (1995) (17)
Genetic and physical mapping of the progressive epilepsy with mental retardation (EPMR) locus on chromosome 8p. (1996) (17)
Refinement of the cone-rod retinal dystrophy locus on chromosome 19q. (1994) (17)
Report of the committee on the genetic constitution of the Y chromosome. (1989) (16)
A transcriptional Map of the FMF region. (1998) (16)
Refined linkage map of chromosome 5 in the region of the spinal muscular atrophy gene. (1993) (16)
Pycnodysostosis: refined linkage and radiation hybrid analyses reduce the critical region to 2 cM at 1q21 and map two candidate genes (1996) (16)
Physical localization of microsatellite markers at the ataxia-telangiectasia locus at 11q22-q23. (1994) (15)
A fine integrated map of the SPG4 locus excludes an expanded CAG repeat in chromosome 2p-linked autosomal dominant spastic paraplegia. (1999) (15)
Pure Familial Spastic Paraplegia: Clinical and Genetic Analysis of Nine Belgian Pedigrees (1996) (15)
Identification and chromosomal localization of human genes containing CAG/CTG repeats expressed in testis and brain. (1997) (15)
ASEtrap: a biological method for speeding up the exploration of spliceomes. (2006) (15)
A 11 Mb YAC-based contig spanning the familial juvenile nephronophthisis region (NPH1) located on chromosome 2q. (1995) (15)
3-Keto-5-aminohexanoate Cleavage Enzyme (2011) (15)
Contrasted Microcolinearity and Gene Evolution Within a Homoeologous Region of Wheat and Barley Species (2008) (15)
Assessing the Drosophila melanogaster and Anopheles gambiae genome annotations using genome-wide sequence comparisons. (2003) (14)
Linkage analyses in British pedigrees suggest a single locus for Darier disease and narrow the location to the interval between D12S105 and D12S129. (1994) (14)
A 4.5-megabase yeast artificial chromosome contig from human chromosome 13q14.3 ordering 9 polymorphic microsatellites (22 sequence-tagged sites) tightly linked to the Wilson disease locus. (1993) (13)
The Primary Structure of tRNAIIArg from Brewers' Yeast (1975) (13)
The Phaeodactylum genome reveals the dynamic nature and multi-lineage evolutionary history of diatom genomes (2011) (13)
Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11–Xq21 microsatellites in a new large family: Three new markers are closely linked to the gene (1994) (13)
Fibulin-2: Genetic Mapping and Exclusion as a Candidate Gene in Marfan Syndrome Type 2 (1996) (13)
FISH-Mapped CEPH YACs spanning 0 to 46 cM on human chromosome 6. (1996) (13)
Precise mapping of t(12;14) leiomyoma breakpoint on chromosome 14 between D14S298 and D14S540. (1995) (13)
An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature (1990) (12)
A Novel Acyl-CoA Beta-Transaminase Characterized from a Metagenome (2011) (12)
Analysis of 148 kb of Genomic DNA of Tetraodon nigroviridis Covering an Amylase Gene Family* (2003) (12)
Nephropathic Cystinosis (CTNS-LSB): Construction of a YAC Contig Comprising the Refined Critical Region on Chromosome 17p13 (1997) (11)
Mapping the human Y chromosome. (1988) (10)
A somatic cell hybrid panel for distal 17q: GDIA1 maps to 17q25.3. (1997) (10)
A high resolution integrated yeast artificial chromosome clone map of human chromosome 22. (1995) (10)
A radiation hybrid map of 95 STSs spanning human chromosome 13q. (1995) (10)
Characterization and mapping of canine polymorphic markers. (1999) (10)
Methylation of an adenosine in the D-loop of specific transfer RNAs from yeast by a procaryotic tRNA (adenine-1) methyltransferase. (1977) (10)
A PCR-based genetic map for human chromosome 3. (1994) (10)
A10-cM YAC Contig Spanning GLC1A, the Primary Open-Angle Glaucoma Locus at 1q23–q25 (1996) (10)
[Primary structure of tRNA Arg/III of brewer's yeast. 2-Partial hydrolysis of tRNA Arg/III by pancreatic and T1 ribonucleases and determination of their complete primary structure]. (1974) (9)
Integrated genetic map of human chromosome 2 (1995) (9)
[Primary structure of tRNA Thr 1a and b from brewer's yeast]. (1977) (9)
CAG/CTG and CGG/GCC repeats in human brain reference cDNAs: outcome in searching for new dynamic mutations. (1998) (9)
Readjusting the localization of long QT syndrome gene on chromosome 11p15. (1995) (9)
Diversity and clustered distribution of retrotransposable elements in the compact genome of the pufferfish Tetraodon nigroviridis (2005) (9)
Regular ArticleThe CEPH Consortium Linkage Map of Human Chromosome 11 (1995) (9)
Genome-wide comparisons between human and tetraodon. (2002) (9)
Effect of threonylcarbamoyl modification in yeast tRNA(III)(Arg) on codon-anticodon and anticodon-anticodon binding: thermodynamic and kinetic evaluations (1980) (8)
Landing on the Genome (1996) (8)
No evidence of genetic heterogeneity in Crouzon craniofacial dysostosis (1995) (8)
A continuous linkage map of 22 short tandem repeat polymorphisms on human chromosome 12. (1993) (8)
Rheumatoid arthritis genome scan and putative autoimmunity locus (1997) (8)
High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1). (1995) (7)
Large α-aminonitrilase activity screening of nitrilase superfamily members: Access to conversion and enantiospecificity by LC–MS (2014) (7)
Genome sequencing: Differences with the relatives (2004) (7)
European Gene Mapping Project (EUROGEM): Breakpoint panels for human chromosomes based on the CEPH reference families (1996) (7)
Recognition of individual procaryotic and eucaryotic transfer-ribonucleic acids by B subtilis adenine-1-methyltransferase specific for the dihydrouridine loop. (1978) (7)
Assignation of highly polymorphic markers on a canine purebred pedigree (2000) (7)
X-Y crossing over in the chimpanzee (1988) (7)
The primary structure of tRNAIIArg from brewers' yeast. 1. Complete digestions with pancreatic and T1 ribonucleases. (1975) (7)
Comparative analysis of BAC and whole genome shotgun sequences from an Anopheles gambiae region related to Plasmodium encapsulation. (2005) (6)
A SAGE approach to identifying novel trans-acting factors involved in the X inactivation process (2006) (6)
The nucleotide sequences of two threonine tRNAs from brewer's yeast (1976) (6)
Identification and mapping of 26 human testis mRNAs containing CAG/CTG repeats (1998) (6)
[Gene localisation in 12q12 in Holt-Oram atrio-digital syndrome]. (1995) (6)
Estimation of the Extent of Synteny Between Tetraodon nigroviridis and Homo sapiens Genomes (2004) (6)
Human genome project: past, present, future. (2002) (5)
Advances in Brief Isolation and Mapping of a Human Septin Gene to a Region on Chromosome 17 q , Commonly Deleted in Sporadic Epithelial Ovarian Tumors 1 (2000) (5)
Sequences homologous to the human y chromosome detected in the female genome (1984) (5)
[Microbiotes and metagenomics]. (2016) (5)
Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegia (1995) (5)
Mapping of DFNB 12 , a gene for a non-syndromal autosomal recessive deafness , to chromosome 10 q 21 – 22 (1996) (5)
Exclusion of genes coding for proteins of the cytoskeleton and the extracellular matrix in familial hypertrophic cardiomyopathy using a candidate gene approach. (1993) (5)
A molecular analysis of the human Y chromosome (1987) (4)
Physical mapping of 30 CA repeats on human chromosome 22. (1995) (4)
The EUROGEM map of human chromosome 5. (1994) (4)
Human genome mapping and sequencing: perspectives for toxicology. (1998) (4)
Physical mapping of the human ELA1 gene between D12S361 and D12S347 on chromosome 12q13. (1995) (4)
Erratum: A radiation hybrid transcript map of the mouse genome (Nature Genetics (2001) 29 (194-200)) (2001) (4)
Construction and characterization of a BAC library for functional genomics in Xenopus tropicalis. (2017) (4)
A first high-density map of 981 biallelic markers on human chromosome 14. (2000) (4)
Poster abstractGenetic heterogeneity in hereditary non-polyposis colon cancer as detected with molecular probes (1994) (4)
The EUROGEM map of human chromosome 20. (1993) (4)
Expression sequence tag library derived from peripheral blood mononuclear cells of the chlorocebus sabaeus (2012) (4)
Isolation of yeast artificial chromosome clones from 54 polymorphic loci mapped with high odds on human chromosome 4. (1994) (3)
Report of the First International Workshop on Human Chromosome 20 Mapping 1993 (1994) (3)
Evidence of chromosomal inversion using fluorescence in situ hybridization to stretched DNA. (1998) (3)
A YAC contig in 6p23 based on sequence tagged sites. (1994) (3)
A polymorphic DNA sequence from the terminal part of chromosome 12q [D12S37]. (1990) (3)
Integrating maps requires integrated data (1996) (3)
Genome-wide analyses based on comparative genomics. (2003) (3)
Gene of the familial Mediterranean fever (1998) (3)
[Familial hemiplegic migraine. Localization of a responsible gene on chromosome 19]. (1994) (3)
The Y Chromosome and Sex Determination (1988) (3)
Exclusion of the cone-specific α-subunit of the transducin gene in Stargardt's disease (1995) (2)
Relative order determination of four Yp cosmids on metaphase and interphase chromosomes by two-color competitive in situ hybridization (1991) (2)
Report of the committee on the genetic constitution of the Y chromosome. (1990) (2)
The primary structure of tRNAIIAgr from brewers' yeast. 2. Partial digestion with ribonuclease T1 and derivation of the complete sequence. (1975) (2)
Physical and genetic mapping of human chromosome 3 loci containing microsatellite repeats (1994) (2)
Regional assignment of human ESTs by whole-genome radiation hybrid mapping (1996) (2)
Genetic Analysis of Citrobacter sp.86 Reveals Involvement of Corrinoids in Chlordecone and Lindane Biotransformations (2020) (2)
A polymorphic DNA sequence from the terminal part of chromosome 21q [D21S154]. (1990) (2)
Exploring biochemical diversity in bacteria. (2019) (2)
Genetic Heterogeneity ofFamilial Hemiplegic Migraine (1994) (2)
Clinical and Genetic Heterogeneity of Leber’s Congenital Amaurosis (1993) (2)
P-113: Search for the gene(s) responsible for lipoatrophic diabetes (2009) (1)
Construction of a highly annotated cosmid contig spanning 550Kb within the X-linked nonspecific mental retardation candidate region at Xp21.3-22.1. (1999) (1)
Establishment of the marker order pter-NRAS-NGFB-D1S189-D1S252-D1S440-D1S453-D1S514-CEN-D1S442-D1S498-qter in relation to the centromere on human chromosome 1 (1995) (1)
[Purification of Arg II tRNA from beer yeasts]. (1972) (1)
Evidence for Locus Heterogeneity in Acrocephalosyndactyly : A Refined Localization for the Saethre-Chotzen Syndrome Locus on Distal Chromosome 7 p-and Exclusion of Jackson-Weiss Syndrome (2007) (1)
Correction to article in Vol 86:252–258 (1999) (2000) (1)
Methylobacterium Genome Sequences; ; PLos one; (2009) (1)
[Clinical and molecular genetic analysis of 4 Swiss families with the pure form of hereditary spastic spinal paralysis]. (1998) (1)
Exclusion of the cone-specific alpha-subunit of the transducin gene in Stargardt's disease. (1995) (1)
Rheumatoid arthritis association with a T-cell receptor genotype. (1996) (1)
[Polymorphisms in the pseudoautosomal regions of X and Y in DNA diagnosis]. (1993) (1)
on the physical , cytogenetic , and genetic maps of chromosome 7 . The human obese ( OB ) gene : RNA expression pattern and mapping (2007) (1)
Expression sequence tag library derived from peripheral blood mononuclear cells of the chlorocebus sabaeus (2012) (1)
9 Fish Genomics and Biology (2006) (1)
Enterotypes of thehumangutmicrobiome (2011) (0)
P582 - Rheumatoid arthritis association with alleles of T-cell receptor α chain is influenced by HLA (1996) (0)
Review Process File (2012) (0)
Extending the cereus group genomics to putative food-borne pathogens of different toxicity (2008) (0)
Isolation and Mapping of a Human SeptinGene to a Region on Chromosome 17q, Commonly Deleted in Sporadic Epithelial Ovarian Tumors (2000) (0)
Interval in Distal 21q (1996) (0)
[A method of molecular hybridization identification of chromosomes purified with a cell sorter]. (1982) (0)
Corrigendum: Parallel evolution of non-homologous isofunctional enzymes in methionine biosynthesis. (2017) (0)
Novel metabolic features in Acinetobacter baylyi ADP1 revealed by a multiomics approach (2014) (0)
An Xp22.1-p22.2 VAC contig encompassing the disease loci for RS, KFSD, CLS, HVP and RP15; refined localization of RS and KFSD. (2014) (0)
Genetic Mapping of the Human Amphiphysin Gene ( AMPH ) at 7 p l 4p 1 3 Excludes Its Involvement in Retinitis Pigmentosa 9 or Dominant Cystoid Macular Dystrophy (2007) (0)
A polymorphic DNA sequence from the terminal part of chromosome 20q [D20S26]. (1990) (0)
[The high fork of genome programs]. (1996) (0)
Sensor and method for diagnosing the sex of a human embryo (1984) (0)
Nucleotide sequence of tRNA(Arg)(II) from brewer's yeast. (1972) (0)
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First Tara Oceans V9 rDNA metabarcoding dataset. (2015) (0)
Nonsyndromic Cleft Lip and Palate : Evidence of Linkage to a Microsatellite Marker on 6 p 23 To the (2007) (0)
Chromosomal assignment of a second locus for Marfan Syndrome To Chromosome 3 p 24 . 2p 25 . (2017) (0)
A polymorphic DNA sequence from the terminal part of chromosome 5p [D5S109]. (1990) (0)
16S rRNA and As-Related Functional Diversity: Contrasting Fingerprints in Arsenic-Rich Sediments from an Acid Mine Drainage (2015) (0)
Acknowledgements We thank R. K. Alagappan and L. G. Brown for technical contributions (2003) (0)
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Comments on the origin of the genetic code: a 27-codon hypothetical precursor of an intricate 64-codon intermediate shaped the modern code. (2021) (0)
The Sequencing of Plant Nuclear Genomes (2013) (0)
Use of Fluorescently Labeled DNA and a Scanner for Electro- phoretic Mobility Shift Assays (2001) (0)
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Lawrence Berkeley National Laboratory Recent Work Title Plankton networks driving carbon export in the oligotrophic ocean Permalink (2016) (0)
Sequences : A Combined Approach to Evaluate and Improve Whole Genome Sequence Comparisons and " Full-Length " cDNA data (2004) (0)
ISOLATION OF GENES FROM A 1.7-MB YAC CONTIG WITHIN THE ESSENTIAL REGION OF X-LINKED EYE DISORDERS (1993) (0)
[The human genome: state of the art]. (1992) (0)
Machado-Joseph Disease inPedigrees ofAzoreanDescent IsLinked toChromosome14 (1994) (0)
[Primary structure of tRNA Arg/III of brewer's yeast. 1. Complete hydrolysis by pancreatic and T1 ribonucleases]. (1974) (0)
The Eukaryote Genome Annotation Platform at Genoscope (2009) (0)
[Primary structure of transfer RNA]. (1972) (0)
features of glomerular parietal cells Atlas of gene expression in the mouse kidney: new (2015) (0)
Enterotypes of the human gut microbiome (Addendum) (2014) (0)
The sequences of nucleotides in tRNA(Arg)(III) from brewer's yeast. (1972) (0)
Genomics : Editorial overview (2007) (0)
Re: Request from the international advisory committee to DDBJ/EMBL/GenBank (2006) (0)
A global ocean atlas of eukaryotic genes (2018) (0)
Single-cell genomics of multiple uncultured stramenopiles reveals underestimated functional diversity across oceans (2018) (0)
A polymorphic DNA sequence from the terminal part of chromosome 20q [D20S25]. (1990) (0)
[First generation of the physical map of the human genome]. (1993) (0)
Genomic Sequence and polypeptides of Pyrococcus abyssi, fragments and their uses (1999) (0)
[Mapping and human genome sequence program]. (1997) (0)
Evolution of multicellularity in the heterokont lineage : analysis of the Ectocarpus siliculosus genome sequence (2009) (0)

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