J. Weissenbach

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A physical map of 30,000 human genes.

P. Lijnzaad, P. Deloukas, E. Lander, 1998, Science.

A radiation hybrid map of the human genome.

G. Gyapay, C. Fizames, J. Morissette, 1996, Human molecular genetics.

A method for constructing radiation hybrid maps of whole genomes

J. Weissenbach, P. Goodfellow, D. Spillett, 1994, Nature Genetics.

A Gene Map of the Human Genome

P. Deloukas, E. Lander, M. Adams, 1996, Science.

Identification and characterization of a spinal muscular atrophy-determining gene

J. Weissenbach, D. Paslier, A. Munnich, 1995, Cell.

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

Bertrand Fontaine, Patrick Wincker, Jean Weissenbach, 1999, Nature Genetics.

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

J. Weissenbach, H. Chabriat, E. Cabanis, 1996, Nature.

A physical map of human chromosome 7: an integrated YAC contig map with average STS spacing of 79 kb.

R. Fulton, J. Weissenbach, E. Green, 1997, Genome research.

A first-generation physical map of the human genome

J. Weissenbach, I. Chumakov, Daniel Cohen, 1993, Nature.

Continuum of overlapping clones spanning the entire human chromosome 21q

X. Estivill, D. Cox, J. Weissenbach, 1992, Nature.

Identification and cloning in yeast artificial chromosomes of a region of elevated loss of heterozygosity on chromosome 1p31.1 in human breast cancer.

J. Weissenbach, J. Varley, Y. Hey, 1995, Genomics.

Allelic imbalance on chromosome I in human breast cancer. II. Microsatellite repeat analysis

J. Weissenbach, A. Howell, J. Varley, 1995, Genes, chromosomes & cancer.

A second-generation linkage map of the human genome

G. Gyapay, J. Morissette, J. Weissenbach, 1992, Nature.

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

J. Weissenbach, D. Paslier, J. Claverie, 1991, Cell.

Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients

J. Weissenbach, H. Chabriat, C. Cruaud, 1997, The Lancet.

Mutations in PCSK9 cause autosomal dominant hypercholesterolemia

J. Weissenbach, N. Seidah, C. Junien, 2003, Nature Genetics.

A second generation linkage map of the human genome based on highly informative microsatellite loci.

J. Weissenbach, J Weissenbach, 1993, Gene.

A comprehensive genetic map of the human genome based on 5,264 microsatellites

Cécile Fizames, Colette Dib, Jean Weissenbach, 1996, Nature.

A linkage study of the N‐methyl‐D‐aspartate receptor subunit gene loci and schizophrenia in southern African Bantu‐speaking families

J. Weissenbach, B. Riley, R. Williamson, 1997, Psychiatric genetics.

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

Robin J. Leach, Paul S. Meltzer, Jean Weissenbach, 1993, Cell.

An STS-Based Map of the Human Genome

L Kruglyak, M P Reeve-Daly, E S Lander, 1995, Science.

The DNA sequence and analysis of human chromosome 14

Patrick Wincker, Jean Weissenbach, Leroy Hood, 2023, Nature.

A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36

Jean Weissenbach, Christine Petit, J. Weissenbach, 1998, European Journal of Human Genetics.

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy.

J. Weissenbach, C. Cruaud, K. Tryggvason, 1995, Nature genetics.

Homology between a 173-kb region from mouse chromosome 10, telomeric to the Ifng locus, and human chromosome 12q15.

J. Weissenbach, C. Robert, F. Bihl, 2001, Genomics.

Evidence that the Saethre-Chotzen syndrome locus lies between D7S664 and D7S507, by genetic analysis and detection of a microdeletion in a patient.

J. Weissenbach, E. Green, M. Summar, 1994, American journal of human genetics.

Localization of a gene causing cystinuria to chromosome 2p

J. Weissenbach, J. Schapiro, D. Kastner, 1994, Nature Genetics.

A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q.

J. Weissenbach, J. Hazan, H. Plauchu, 1995, Human molecular genetics.

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.

J. Weissenbach, Y. Agid, A. Brice, 1996, American journal of human genetics.

The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16.

M. Polymeropoulos, J. Weissenbach, J. Goodship, 1996, Genomics.

Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis

J. Weissenbach, A. Chapelle, P. Sistonen, 1994, Nature Genetics.

Notch3 Mutations in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL), a Mendelian Condition Causing Stroke and Vascular Dementia

J. Weissenbach, H. Chabriat, E. Cabanis, 1997, Annals of the New York Academy of Sciences.

Loss of the chromosomal region 10q23-25 in prostate cancer.

J. Weissenbach, I. Gray, J. Neoptolemos, 1995, Cancer research.

A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13.

J. Weissenbach, A. Munnich, E. Souied, 1995, American journal of human genetics.

Genetic heterogeneity of Usher syndrome type 1 in French families.

J. Weissenbach, D. Bonneau, J. Dufier, 1994, Genomics.

Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy

J. Weissenbach, C. Cruaud, K. Tryggvason, 1995, Nature Genetics.

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.

J. Weissenbach, H. Cavé, B. Gérard, 1995, Blood.

Single-copy DNA sequences specific for the human Y chromosome

J. Weissenbach, G. Guellaen, M. Fellous, 1983, Nature.

An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3.

J. Weissenbach, D. Schlessinger, G. Borsani, 1995, Human molecular genetics.

Chromosome 9p deletions in cutaneous malignant melanoma tumors: the minimal deleted region involves markers outside the p16 (CDKN2) gene.

X. Estivill, J. Weissenbach, S. Puig, 1995, American journal of human genetics.

Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus

J. Beckmann, J. Weissenbach, K. Clément, 1992, Nature.

Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11.

G. Gyapay, T. Hudson, J. Weissenbach, 1999, American journal of human genetics.

Microsatellite-based fine mapping of the Van der Woude syndrome locus to an interval of 4.1 cM between D1S245 and D1S414.

J. Weissenbach, K. Buetow, R. Schmelzle, 1995, American journal of human genetics.

A common gene for juvenile and adult-onset primary open-angle glaucomas confined on chromosome 1q.

J. Morissette, J. Weissenbach, G. Trope, 1995, American journal of human genetics.

An Xp22.1-p22.2 VAC contig encompassing the disease loci for RS, KFSD, CLS, HVP and RP15; refined localization of RS and KFSD.

J. Weissenbach, S. Gregory, J. Oosterwijk, 2014 .

A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family

J. Weissenbach, M. Bitner-Glindzicz, R. Heilig, 1997, Nature Genetics.

Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1.

J. Weissenbach, M. Lathrop, J. Prud'homme, 2002, Human molecular genetics.

CAG/CTG and CGG/GCC repeats in human brain reference cDNAs: outcome in searching for new dynamic mutations.

J. Weissenbach, H. Cann, S. Meier-Ewert, 1998, Genomics.

The human obese (OB) gene: RNA expression pattern and mapping on the physical, cytogenetic, and genetic maps of chromosome 7.

J. Weissenbach, E. Green, U. DeSilva, 1995, Genome research.

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.

G. Gyapay, J. Weissenbach, J. Auwerx, 1998, Diabetes.

The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2.

J. Weissenbach, H. Cann, Y. Agid, 1995, American journal of human genetics.

The gene for Machado–Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14q

J. Weissenbach, Y. Agid, A. Dürr, 1994, Neurobiology of Disease.

The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of ∼3 cM on chromosome 14q24.3-q32.2

J. Weissenbach, H. Cann, Y. Agid, 1995 .

The spinocerebellar ataxia 2 locus is located within a 3-cM interval on chromosome 12q23-24.1.

J. Weissenbach, R. Williamson, M. Pook, 1995, American journal of human genetics.

Evidence of chromosomal inversion using fluorescence in situ hybridization to stretched DNA.

J. Weissenbach, D. Campion, R. Berger, 1998, Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie.

Physical mapping of the human pseudo‐autosomal region; comparison with genetic linkage map.

J. Weissenbach, C. Petit, J. Levilliers, 1988, The EMBO journal.

Localization and expression analysis of a novel conserved brain expressed transcript, Brx/BRX, lying within the Xic/XIC candidate region

J. Weissenbach, P. Avner, E. Heard, 1997, Mammalian Genome.

The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8.

J. Weissenbach, A. de la Chapelle, P. Sistonen, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Extensive sequence homologies between Y and other human chromosomes.

J. Weissenbach, G. Guellaen, M. Fellous, 1984, Journal of molecular biology.

A DNA probe detecting multiple haplotypes of the human Y chromosome.

J. Weissenbach, G. Vergnaud, G. Lucotte, 1986, American journal of human genetics.

Refining the localization of the PKD2 locus on chromosome 4q by linkage analysis in Spanish families with autosomal dominant polycystic kidney disease type 2.

J. Weissenbach, F. Moreno, J. L. San Millán, 1995, American journal of human genetics.

Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity.

J. Weissenbach, T. Klockgether, T. Voit, 1995, American journal of human genetics.

No evidence of genetic heterogeneity in Crouzon craniofacial dysostosis

J. Weissenbach, A. Munnich, D. Rénier, 1995, Human Genetics.

Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13

J. Weissenbach, A. Munnich, H. Dollfus, 1996, Human Genetics.

Aicardi–Goutières syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?

J. Weissenbach, G. Ponsot, P. Lebon, 1999, Clinical genetics.

Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy.

J. Weissenbach, K. Bushby, F. Muntoni, 1997, Journal of medical genetics.

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.

J. Weissenbach, C. Cruaud, K. Tryggvason, 1996, American journal of human genetics.

Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families.

G. Gyapay, J. Weissenbach, D. Le Paslier, 1995, American journal of human genetics.

Use of genetic and physical mapping to locate the spinal muscular atrophy locus between two new highly polymorphic DNA markers.

J. Weissenbach, J. McPherson, D. Le Paslier, 1994, American journal of human genetics.

Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A

J. Weissenbach, A. Dürr, A. Brice, 2004, Neurogenetics.

A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites.

J. Beckmann, J. Weissenbach, A. Bowcock, 1993, Human molecular genetics.

A novel gene that encodes a protein with a putative src homology 3 domain is a candidate gene for familial juvenile nephronophthisis.

J. Weissenbach, R. Heilig, F. Silbermann, 1997, Human molecular genetics.

Characterization and mapping of canine polymorphic markers.

J. Weissenbach, S. Fauré, S. Bentolila, 1999, Animal genetics.

Close mapping of the focal non-epidermolytic palmoplantar keratoderma (PPK) locus associated with oesophageal cancer (TOC).

J. Weissenbach, D. Bishop, D. Kelsell, 1996, Human molecular genetics.

Pure Familial Spastic Paraplegia: Clinical and Genetic Analysis of Nine Belgian Pedigrees

J. Weissenbach, C. Broeckhoven, J. Hazan, 1996, European journal of human genetics : EJHG.

Genetic and physical characterization of the early-onset Alzheimer's disease AD3 locus on chromosome 14q24.3.

J. Weissenbach, D. Le Paslier, A. Goate, 1995, Human molecular genetics.

New susceptibility locus for rheumatoid arthritis suggested by a genome-wide linkage study.

G. Gyapay, J. Weissenbach, J. Prud'homme, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Correlations of allelic imbalance of chromosome 14 with adverse prognostic parameters in 148 renal cell carcinomas

J. Weissenbach, C. Béroud, Y. Chrétien, 1996, Genes, chromosomes & cancer.

High-density genetic map of the BRCA1 region of chromosome 17q12-q21.

M. King, J. Weissenbach, A. Bowcock, 1993, Genomics.

Exclusion of HRAS from long QT locus

J. Weissenbach, P. Coumel, M. Komajda, 1994, Nature Genetics.

The 1993–94 Généthon human genetic linkage map

Cécile Fizames, Colette Dib, Jean Weissenbach, 1994, Nature Genetics.

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

J. Weissenbach, J. Varley, Y. Hey, 1995, Chromosome Research.

An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p.

L. Peltonen, J. Weissenbach, G. Comi, 1996, American journal of human genetics.

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).

J. Weissenbach, D. Le Paslier, A. Ballabio, 1995, Genomics.

The Sjögren-Larsson Syndrome gene is close to D17S805 as determined by linkage analysis and allelic association

J. Weissenbach, C. Wadelius, K. Gustavson, 1994, Nature Genetics.

Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis

Albert David, Jean Weissenbach, José-Alain Sahel, 2011, Orphanet journal of rare diseases.

Mapping of Microsatellite Markers in the Alagille Region and Screening of Microdeletions by Genotyping 23 Patients

J. Weissenbach, J. Deleuze, J. Hazan, 1994, European journal of human genetics : EJHG.

Readjusting the localization of long QT syndrome gene on chromosome 11p15.

J. Weissenbach, P. Coumel, P. Kahlem, 1995, Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie.

Age and origin of two common MLH1 mutations predisposing to hereditary colon cancer.

Chapelle, J. Weissenbach, A. de la Chapelle, 1996, American journal of human genetics.

Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer families.

J. Weissenbach, L. Aaltonen, A. de la Chapelle, 1994, Proceedings of the National Academy of Sciences of the United States of America.

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex

J. Haines, G. Gyapay, J. Weissenbach, 1996, Nature Genetics.

Rapid and early determination of sex using trophoblast biopsy specimens and Y chromosome specific DNA probes.

J. Weissenbach, R. Berger, G. Guellaen, 1984, British medical journal.

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.

J. Weissenbach, W. Reardon, R. Winter, 1994, American journal of human genetics.

Rheumatoid arthritis genome scan and putative autoimmunity locus

J. Weissenbach, C. Dib, P. Migliorini, 1997 .

A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene.

J. Weissenbach, D. Le Paslier, H. Chaib, 1994, Human molecular genetics.

Construction of a YAC contig and a STS map spanning at least seven megabasepairs in chromosome 5q34-35.

J. Weissenbach, D. Le Paslier, D. Ward, 1994, Human molecular genetics.

The genetic locus for free sialic acid storage disease maps to the long arm of chromosome 6.

L. Peltonen, J. Weissenbach, J. Schleutker, 1994, American journal of human genetics.

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.

J. Weissenbach, G. Auburger, A. Lunkes, 1995, American journal of human genetics.

A PCR-based genetic map for human chromosome 3.

J. Weissenbach, P. O'Connell, L. Ballard, 1994, Genomics.

A high-density microsatellite map of the ataxia-telangiectasia locus

V. Sheffield, M. James, J. Weissenbach, 1995, Human Genetics.

Refinement of the cone-rod retinal dystrophy locus on chromosome 19q.

J. Weissenbach, S. Bhattacharya, A. Fryer, 1994, American journal of human genetics.

Conservation of human-derived pseudoautosomal sequences on the sex chromosomes of the great apes.

J. Weissenbach, W. Schempp, B. Weber, 1987, Cytogenetics and cell genetics.

Genetic linkage analysis in hereditary non-polyposis colon cancer syndrome.

J. Weissenbach, B. Ponder, D. Evans, 1995, Journal of medical genetics.

Nonsyndromic Cleft Lip and Palate : Evidence of Linkage to a Microsatellite Marker on 6 p 23 To the

J. Weissenbach, R. Williamson, R. Twells, 2007 .

Report of the committee on the genetic constitution of the Y chromosome.

J. Weissenbach, P. Goodfellow, K. Smith, 1988, Cytogenetics and cell genetics.

Positional candidate genes for congenital chloride diarrhea suggested by high-resolution physical mapping in chromosome region 7q31.

S. Scherer, J. Weissenbach, L. Tsui, 1996, Genome research.

Vector integration is nonrandom and clustered and influences the fate of lymphopoiesis in SCID-X1 gene therapy.

Bruce Aronow, Christof von Kalle, Jean Weissenbach, 2007, The Journal of clinical investigation.

A gene for achondroplasia–hypochondroplasia maps to chromosome 4p

Jean Weissenbach, Arnold Munnich, Martine Le Merrer, 1994, Nature Genetics.

Pseudoautosomal DNA sequences in the pairing region of the human sex chromosomes

J. Weissenbach, A. Chapelle, G. Vergnaud, 1985, Nature.

Characterization of the NPHP1 locus: mutational mechanism involved in deletions in familial juvenile nephronophthisis.

J. Weissenbach, R. Heilig, F. Silbermann, 2000, American journal of human genetics.

A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomes

J. Weissenbach, G. Vergnaud, F. Rouyer, 1986, Nature.

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.

J. Weissenbach, D. Bishop, D. Kelsell, 1996, Archives of dermatology.

The gene for Darier's disease maps between D12S78 and D12S79.

N. Craddock, J. Weissenbach, P. McGuffin, 1994, Human molecular genetics.

Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome.

J. Weissenbach, R. Heilig, M. Lathrop, 2001, American journal of human genetics.

A placenta-specific receptor for the fusogenic, endogenous retrovirus-derived, human syncytin-2

J. Weissenbach, T. Bruls, T. Heidmann, 2008, Proceedings of the National Academy of Sciences.

Mapping of a second locus for lamellar ichthyosis to chromosome 2q33-35.

J. Weissenbach, L. Dubertret, C. Blanchet‐Bardon, 1996, Human molecular genetics.

Linkage of the gene for cystinosis to markers on the short arm of chromosome 17

M. Polymeropoulos, J. Weissenbach, C. Mathew, 1995, Nature Genetics.

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene

Sahar Mansour, Jean Weissenbach, J. Weissenbach, 1994, Nature.

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.

J. Weissenbach, A. Reis, C. Mcconville, 1994, Genomics.

A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10

J. Weissenbach, A. Munnich, M. Devoto, 1993, Nature Genetics.

Genetic and physical mapping of the Chediak-Higashi syndrome on chromosome 1q42-43.

J. Weissenbach, D. Le Paslier, D. Paslier, 1996, American journal of human genetics.

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

T. Matise, J. Weissenbach, A. Chakravarti, 1994, Human molecular genetics.

A deletion map of the human Y chromosome based on DNA hybridization.

D. Botstein, J. Weissenbach, L. Brown, 1986, American journal of human genetics.

Ring Y chromosome: molecular characterization by DNA probes.

J. Weissenbach, G. Rappold, D. Ahlert, 1991, Cytogenetics and cell genetics.

Report of the committee on the genetic constitution of the Y chromosome.

J. Weissenbach, P. Goodfellow, K. Smith, 1989, Cytogenetics and cell genetics.

An abnormal terminal X-Y interchange accounts for most but not all cases of human XX maleness

J. Weissenbach, A. Chapelle, C. Petit, 1987, Cell.

Chromosome Y-specific DNA in related human XX males

J. Weissenbach, D. Page, A. Chapelle, 1985, Nature.

Human XX males with Y single-copy DNA fragments

J. Weissenbach, G. Guellaen, M. Fellous, 1984, Nature.

Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.

J. Weissenbach, R. Heilig, M. Lathrop, 2003, Human molecular genetics.

A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2p

J. Beckmann, J. Weissenbach, C. Antignac, 1993, Nature Genetics.

Mapping of a susceptibility locus for Crohn's disease on chromosome 16

Jean Weissenbach, Laurent Beaugerie, Pierre Laurent-Puig, 1996, Nature.

A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish

J. Weissenbach, J. Ott, S. Paul, 1996, Nature Genetics.

An international two–stage genome–wide search for schizophrenia susceptibility genes

J. Weissenbach, K. Kidd, A. Pakstis, 1995, Nature Genetics.

Evidence of a non-MHC susceptibility locus in type I diabetes linked to HLA on chromosome 6.

J. Weissenbach, J. Rotter, P. Froguel, 1997, American journal of human genetics.

Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23

S. Barondes, J. Weissenbach, M. Escamilla, 1996, Nature Genetics.

Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome llq

M. James, J. Weissenbach, G. Lathrop, 1994, Nature.

Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellites.

J. Weissenbach, L. Cavalli-Sforza, L. Cavalli-Sforza, 1994, American journal of human genetics.

The CEPH consortium linkage map of human chromosome 16.

H Donis-Keller, H M Kozman, T P Keith, 1994, Genomics.

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.

J. Morissette, J. Weissenbach, E. Shink, 1999, American journal of medical genetics.

Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians.

J. Weissenbach, D. Labuda, F. Glorieux, 1996, American journal of human genetics.

Random search for shared chromosomal regions in four affected individuals: the assignment of a new hereditary ataxia locus.

L. Peltonen, J. Weissenbach, J. Terwilliger, 1995, American journal of human genetics.

A 94 kb genomic sequence 3' to the murine Xist gene reveals an AT rich region containing a new testis specific gene Tsx.

J. Weissenbach, P. Avner, J. Claverie, 1996, Human molecular genetics.

An autosomal locus predisposing to deletions of mitochondrial DNA

L. Peltonen, J. Weissenbach, M. Zeviani, 1995, Nature Genetics.

The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21–q24

L. Peltonen, J. Weissenbach, R. Salonen, 1995, Nature Genetics.

Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19.

L. Peltonen, G. Gyapay, J. Weissenbach, 1994, American journal of human genetics.

The Y Chromosome and Sex Determination

J. Weissenbach, F. Rouyer, 1988, The Lancet.

Linkage analyses in British pedigrees suggest a single locus for Darier disease and narrow the location to the interval between D12S105 and D12S129.

J. Weissenbach, R. Kucherlapati, E. Healy, 1994, Genomics.

Mutations in the gene encoding SLURP-1 in Mal de Meleda.

J. Weissenbach, R. Heilig, M. Lathrop, 2001, Human molecular genetics.

Genetic linkage of progressive pseudorheumatoid dysplasia to a 3-cM interval of chromosome 6q22

J. Weissenbach, T. Bruls, J. Prud'homme, 1998, Human Genetics.

Human genome anatomy: BACs integrating the genetic and cytogenetic maps for bridging genome and biomedicine.

B. Birren, L. Hui, X. Wu, 1999, Genome research.

Survey of CAG/CTG repeats in human cDNAs representing new genes: candidates for inherited neurological disorders.

J. Weissenbach, H. Cann, S. Meier-Ewert, 1996, Human molecular genetics.

Human genome mapping and sequencing: perspectives for toxicology.

J. Weissenbach, 1998, Toxicology letters.

The Human Genome Project: From Mapping to Sequencing

J. Weissenbach, 1998, Clinical chemistry and laboratory medicine.

A radiation hybrid map of 506 STS markers spanning human chromosome 11

G. M. Lathrop, M. Polymeropoulos, M. James, 1994, Nature Genetics.

Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1.

J. Weissenbach, R. Heilig, D. Samson, 1997, Human molecular genetics.

Mapping the human Y chromosome.

J. Weissenbach, 1988, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development

J. Weissenbach, A. Munnich, C. Cruaud, 2005, Journal of Medical Genetics.

Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q.

R. Myers, D. Cox, J. Weissenbach, 1996, American journal of human genetics.

Interval in Distal 21q

R. Myers, D. Cox, J. Weissenbach, 1996 .

Selective intestinal malabsorption of vitamin B12 displays recessive mendelian inheritance: assignment of a locus to chromosome 10 by linkage.

J. Weissenbach, R. Gräsbeck, A. de la Chapelle, 1995, American journal of human genetics.

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.

L. Peltonen, J. Weissenbach, J. Schleutker, 1995, American journal of human genetics.

Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysis.

J. Weissenbach, A. de la Chapelle, P. Sistonen, 1995, Genomics.

Linkage analysis of candidate myelin genes in familial multiple sclerosis

J. Haines, M. Pericak-Vance, G. Gyapay, 1999, Neurogenetics.

Autosomal recessive lamellar ichthyosis: identification of a new mutation in transglutaminase 1 and evidence for genetic heterogeneity.

J. Weissenbach, J. Prud'homme, L. Dubertret, 1995, Human molecular genetics.

A physical map of human chromosome 14

Eric Pelletier, Asao Fujiyama, Lee Rowen, 2001, Nature.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12

J. Weissenbach, G. Lathrop, J. Melki, 1993, Nature Genetics.

Report of the First International Workshop on Human Chromosome 20 Mapping 1993.

J. Weissenbach, D. Bowden, T. Keith, 1994, Cytogenetics and cell genetics.

A high resolution integrated yeast artificial chromosome clone map of human chromosome 22.

R. Durbin, N. Carter, J. Collins, 1995 .

Cell complementation using Genebridge 4 human:rodent hybrids for physical mapping of novel mitochondrial respiratory chain deficiency genes.

P. Bénit, G. Gyapay, J. Weissenbach, 2002, Human molecular genetics.

No evidence of genetic heterogeneity in dominant optic atrophy.

J. Weissenbach, A. Munnich, E. Souied, 1995, Journal of medical genetics.

Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome.

J. Weissenbach, M. Lathrop, J. Prud'homme, 2003, Human molecular genetics.

Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig.

J. Weber, J. Weissenbach, L. Morrison, 1995, Genome research.

A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21.

J. Weissenbach, A. Munnich, H. Chaib, 1997, Human molecular genetics.

Identification of three distinct regions of allelic deletions on the short arm of chromosome 8 in hepatocellular carcinoma

G. Gyapay, J. Weissenbach, M. Buendia, 1999, Oncogene.

A subtracted cDNA library from the zebrafish (Danio rerio) embryonic inner ear.

J. Weissenbach, C. Petit, D. Weil, 2002, Genome research.

Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia)

J. Weissenbach, P. Beighton, D. Samson, 2000, Nature Genetics.

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

J. Weissenbach, P. Beighton, M. Hamida, 1996, Human Genetics.

Localization of the Schwartz-Jampel syndrome (SJS) locus to chromosome 1p34-p36.1 by homozygosity mapping.

J. Weissenbach, P. Beighton, D. Viljoen, 1995, Human molecular genetics.

The pseudoautosomal region of the human sex chromosomes.

J. Weissenbach, C. Petit, G. Vergnaud, 1986, Cold Spring Harbor symposia on quantitative biology.

Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.

J. Weissenbach, J. Burgunder, J. Prud'homme, 2000, Human molecular genetics.

Non-specific X-linked mental retardation: linkage analysis in MRX2 and MRX4 families revisited.

J. Weissenbach, J. Mandel, A. Hanauer, 1994, American journal of medical genetics.

A new family linked to the RP13 locus for autosomal dominant retinitis pigmentosa on distal 17p.

J. Weissenbach, A. Bird, S. Bhattacharya, 1996, Journal of medical genetics.

Fine localization of the locus for autosomal dominant retinitis pigmentosa on chromosome 17p.

J. Weissenbach, P. Beighton, Y. Shugart, 1995, American journal of human genetics.

A YAC contig spanning the dominant retinitis pigmentosa locus (RP9) on chromosome 7p.

J. Weissenbach, R. White, A. Cunningham, 1995, Genomics.

X-Y crossing over in the chimpanzee

J. Weissenbach, W. Schempp, B. Weber, 1988, Human Genetics.

Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus

J. Beckmann, J. Weissenbach, K. Clément, 1992, Nature.

European Gene Mapping Project (EUROGEM): Breakpoint panels for human chromosomes based on the CEPH reference families

J. Weissenbach, H. Cann, R. Vossen, 1996, Annals of human genetics.

A genetic linkage map of human chromosome 20 composed entirely of microsatellite markers.

J. Weissenbach, C. Dubay, J. Hazan, 1992, Genomics.

Isolation of yeast artificial chromosome clones from 54 polymorphic loci mapped with high odds on human chromosome 4.

D. Cox, J. Weissenbach, K. Buetow, 1994, Human molecular genetics.

A radiation hybrid transcript map of the mouse genome

Hans Lehrach, Roger D. Cox, Jean Weissenbach, 2001, Nature Genetics.

Loss of heterozygosity in sporadic breast tumours at the BRCA2 locus on chromosome 13q12-q13.

P. Devilee, J. Weissenbach, M. Stratton, 1995, British Journal of Cancer.

Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q.

G. Gyapay, N. Drouot, C. Fizames, 1998, Genome research.

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.

G. Gyapay, J. Weissenbach, O. Jaillon, 2001, Genome research.

Clinical and genetic heterogeneity of hypochondroplasia.

J. Weissenbach, A. Munnich, J. Bonaventure, 1996, Journal of medical genetics.

Microsatellite polymorphisms and the genetic linkage map of the human genome.

J. Weissenbach, Jean Weissenbach, 1993, Current opinion in genetics & development.

Precise mapping of t(12;14) leiomyoma breakpoint on chromosome 14 between D14S298 and D14S540.

J. Weissenbach, R. White, S. Gerken, 1995, Cancer Letters.

Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF).

J. Weissenbach, A. Bernot, C. Cruaud, 1998, Human molecular genetics.

Highly homologous loci on the X and Y chromosomes are hot–spots for ectopic recombinations leading to XX maleness

A. Poustka, J. Weissenbach, C. Petit, 1994, Nature Genetics.

A sex chromosome rearrangement in a human XX male caused by Alu—Alu recombination

J. Weissenbach, D. Page, F. Rouyer, 1987, Cell.

European Gene Mapping Project (EUROGEM): Genetic Maps based on the CEPH reference families

J. Weissenbach, H. Cann, J. Attwood, 1994, European journal of human genetics : EJHG.

A locus for Fanconi anemia on 16q determined by homozygosity mapping.

E. Lander, D. Botstein, J. Weissenbach, 1996, American journal of human genetics.

Linkage disequilibrium utilized to establish a refined genetic position of the Salla disease locus on 6q14-q15.

L. Peltonen, J. Weissenbach, J. Schleutker, 1995, Genomics.

A gene for familial hemiplegic migraine maps to chromosome 19

J. Weissenbach, G. Lathrop, H. Chabriat, 1993, Nature Genetics.

A10-cM YAC Contig Spanning GLC1A, the Primary Open-Angle Glaucoma Locus at 1q23–q25

J. Morissette, J. Weissenbach, C. Desmaze, 1996, European journal of human genetics : EJHG.

A fine integrated map of the SPG4 locus excludes an expanded CAG repeat in chromosome 2p-linked autosomal dominant spastic paraplegia.

G. Gyapay, C. Fizames, D. Muselet, 1999, Genomics.

A calcium channel mutation causing hypokalemic periodic paralysis.

J. Weissenbach, P. Powers, A. Elbaz, 1994, Human molecular genetics.

The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q.

J. Weissenbach, Í. Lopes-Cendes, F. Andermann, 1996, American journal of human genetics.

Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22.

J. Weissenbach, H. Chaib, C. Petit, 1996, Human molecular genetics.

Machado-Joseph disease in four Chinese pedigrees

J. Weissenbach, S. Tsuji, Y. Takiyama, 1997, Neurology.

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

J. Weissenbach, W. Reardon, R. Winter, 2007 .

Genetic Mapping in the Xp11.2 Region of a New Form of X-Linked Hypophosphatemic Rickets

J. Weissenbach, M. Devoto, C. Zoccali, 1993, European journal of human genetics : EJHG.

Two new loci for autosomal recessive ichthyosis on chromosomes 3p21 and 19p12-q12 and evidence for further genetic heterogeneity.

J. Weissenbach, J. Prud'homme, J. Fischer, 2000, American journal of human genetics.

Fibulin-2: Genetic Mapping and Exclusion as a Candidate Gene in Marfan Syndrome Type 2

J. Weissenbach, R. Timpl, Takako Sasaki, 1996, European journal of human genetics : EJHG.

A second locus for Marfan syndrome maps to chromosome 3p24.2–p25

J. Weissenbach, C. Junien, M. Babron, 1994, Nature Genetics.

A SAGE approach to identifying novel trans-acting factors involved in the X inactivation process

J. Weissenbach, P. Avner, C. Ciaudo, 2006, Cytogenetic and Genome Research.

The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac α and β myosin heavy chain genes on chromosome 14q11.2−q13

J. Weissenbach, M. Sanson, S. Blumen, 1995 .

The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac alpha and beta myosin heavy chain genes on chromosome 14q11.2-q13.

J. Weissenbach, M. Sanson, J. Bouchard, 1995, Human molecular genetics.

Long-range restriction map of the terminal part of the short arm of the human X chromosome.

J. Weissenbach, C. Petit, J. Levilliers, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Isolation of sequences from Xp22.3 and deletion mapping using sex chromosome rearrangements from human X-Y interchange sex reversals.

J. Weissenbach, C. Petit, F. Rouyer, 1990, Genomics.

Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22.

A. Monaco, J. Weissenbach, D. Schlessinger, 1995, Human molecular genetics.

A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23.

J. Weissenbach, C. Petit, S. Chardenoux, 1996, Human molecular genetics.

Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31–32 in three European families

J. Weissenbach, N. Baumann, A. Elbaz, 1994, Nature Genetics.

Identification and mapping of 26 human testis mRNAs containing CAG/CTG repeats

G. Gyapay, J. Weissenbach, W. Ansorge, 1998, Mammalian Genome.

Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p.

J. Weissenbach, J. Prud'homme, J. Pouget, 1998, Journal of medical genetics.

A radiation hybrid map of 95 STSs spanning human chromosome 13q.

T. Matise, J. Weissenbach, C. W. Richard, 1995, Genomics.

Identification and chromosomal localization of human genes containing CAG/CTG repeats expressed in testis and brain.

G. Gyapay, N. Chiannilkulchai, J. Weissenbach, 1997, Genome research.

A linkage study of the N-methyl-D-aspartate receptor subunit gene loci and schizophrenia in southern African Bantu-speaking families.

J. Weissenbach, B. Riley, R. Williamson, 1996 .

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.

J. Weissenbach, Y. Agid, R. Sherrington, 1996, Human molecular genetics.

Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14

J. Haines, J. Weissenbach, R. Griggs, 1995, Neurology.

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

J. Weissenbach, P. Devilee, C. Cornelisse, 1996, European journal of human genetics : EJHG.

Chromosomal assignment of a second locus for Marfan Syndrome To Chromosome 3 p 24 . 2p 25 .

J. Weissenbach, C. Junien, M. Babron, 2017 .

Haplotype analysis in gelsoiin‐related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and Japan

T. Paunio, L. Peltonen, J. Weissenbach, 1995, Human mutation.

Sequence and analysis of chromosome 3 of the plant Arabidopsis thaliana.

W Ansorge, H Erfle, G Kauer, 2000, Nature.

A human Y-linked DNA polymorphism and its potential for estimating genetic and evolutionary distance.

J. Weissenbach, P. Leroy, M. Fellous, 1985, Science.

The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1

J. Weissenbach, Y. Agid, C. Broeckhoven, 1995, Nature Genetics.

Physical mapping of the human ELA1 gene between D12S361 and D12S347 on chromosome 12q13.

J. Weissenbach, R. Kucherlapati, R. Davies, 1995, Genomics.

A YAC contig in 6p23 based on sequence tagged sites.

J. Weissenbach, D. Le Paslier, H. Cann, 1994, Genomics.

on the physical , cytogenetic , and genetic maps of chromosome 7 . The human obese ( OB ) gene : RNA expression pattern and mapping

J. Weissenbach, E. Green, U. DeSilva, 2007 .

An interspersed repeated sequence specific for human subtelomeric regions.

J. Weissenbach, A. Chapelle, F. Rouyer, 1990, The EMBO journal.

Confirmation of genetic heterogeneity in familial psoriasis.

J. Weissenbach, R. Williamson, L. Fry, 1995, Journal of medical genetics.

Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12

J. Weissenbach, S. Pulst, Í. Lopes-Cendes, 1996, Neurology.

A second-generation YAC contig map of human chromosome 3.

J. Weissenbach, P. Rigault, J. Cypser, 1995, Nature.

Mapping of DFNB 12 , a gene for a non-syndromal autosomal recessive deafness , to chromosome 10 q 21 – 22

J. Weissenbach, C. Petit, S. Chardenoux, 1996 .

A gene for Holt–Oram syndrome maps to the distal long arm of chromosome 12

J. Weissenbach, A. Munnich, S. Lyonnet, 1994, Nature Genetics.

The gene for triphalangeal thumb maps to the subtelomeric region of chromosome 7q

Jean Weissenbach, Peter Heutink, Ben A. Oostra, 1994, Nature Genetics.

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).

J. Weissenbach, F. Crozet, D. Weil, 1995, Genomics.

DNA replication origin interference increases the spacing between initiation events in human cells.

J. Weissenbach, R. Heilig, R. Lebofsky, 2006, Molecular biology of the cell.

Relative order determination of four Yp cosmids on metaphase and interphase chromosomes by two-color competitive in situ hybridization

J. Weissenbach, A. Bernheim, G. Danglot, 1991, Human Genetics.

Genetic exclusion of 14 candidate genes in lipoatropic diabetes using linkage analysis in 10 consanguineous families.

J. Weissenbach, C. Vigouroux, J. Capeau, 1997, The Journal of clinical endocrinology and metabolism.

Improved PCR-walking for large-scale isolation of plant T-DNA borders.

M Caboche, J. Weissenbach, F. Samson, 2001, BioTechniques.

Association of rheumatoid arthritis with an amino acid allelic variation of the T cell receptor.

J. Weissenbach, J. Prud'homme, K. Pile, 1997, Arthritis and rheumatism.

A 45,X male with a Yp/18 translocation

J. Weissenbach, W. Schempp, M. Fraccaro, 1986, Human Genetics.

An Xp22.1–p22.2 YAC Contig Encompassing the Disease Loci for RS, KFSD, CLS, HYP and RP15: Refined Localization of RS

J. Weissenbach, S. Gregory, J. T. Dunnen, 1996, European journal of human genetics : EJHG.

Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12.

J. Beckmann, J. Weissenbach, A. Vignal, 1993, Human molecular genetics.

Linkage disequilibrium mapping of the cornea plana congenita gene CNA2.

J. Weissenbach, A. de la Chapelle, P. Sistonen, 1995, Genomics.

Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian families.

J. Weissenbach, M. Passos-Bueno, I. Richard, 1993, Journal of medical genetics.

Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2p.

J. Weissenbach, D. Le Paslier, K. Bushby, 1996, Genomics.

A non–syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q

J. Weissenbach, C. Petit, S. Blanchard, 1994, Nature Genetics.

Fine mapping of Best's macular dystrophy localizes the gene in close proximity to but distinct from the D11S480/ROM1 loci.

J. Weissenbach, C. Larsson, C. Graff, 1994, Genomics.

Integrated genetic map of human chromosome 2

H Donis-Keller, A Collins, S P Bryant, 1995, Annals of human genetics.

An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature

J. Weissenbach, J. Melki, C. Petit, 1990, Human Genetics.

A transcriptional Map of the FMF region.

G. Gyapay, N. Chiannilkulchai, C. Fizames, 1998, Genomics.

Two highly polymorphic minisatellites from the pseudoautosomal region of the human sex chromosomes.

J. Weissenbach, C. Petit, G. Vergnaud, 1987, The EMBO journal.

Regular ArticleThe CEPH Consortium Linkage Map of Human Chromosome 11

J. Weber, J. Weissenbach, K. Kidd, 1995 .

The CEPH consortium linkage map of human chromosome 11.

J. Weissenbach, R. White, R. Gatti, 1995, Genomics.

Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)

J. Weissenbach, A. Elbaz, F. Lehmann-Horn, 1994, Human Genetics.

A molecular analysis of the human Y chromosome

J. Weissenbach, 1987 .

Sequences homologous to the human y chromosome detected in the female genome

J. Weissenbach, G. Guellaen, M. Fellous, 1984 .

Normal and abnormal interchanges between the human X and Y chromosomes.

J. Weissenbach, C. Petit, F. Rouyer, 1987, Development.

Extensive DNA sequence homologies between the human Y and the long arm of the X chromosome.

J. Weissenbach, J. Mandel, G. Vergnaud, 1985, The EMBO journal.

A fourth locus for autosomal dominant hypercholesterolemia maps at 16q22.1

J. Weissenbach, A. Munnich, C. Junien, 2010, European Journal of Human Genetics.

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

J. Weissenbach, M. Lathrop, J. Prud'homme, 2001 .

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.

E. Stewart, J. Weissenbach, D. Le Paslier, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Exchange of terminal portions of X- and Y-chromosomal short arms in human XY females.

J. Weissenbach, C. Petit, J. Levilliers, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Absence of Y-specific DNA sequences in human 46,XX true hermaphrodites and in 45,X mixed gonadal dysgenesis

J. Weissenbach, M. Fraccaro, U. Wolf, 1987, Human Genetics.

Mapping of Papillon-Lefèvre Syndrome to the Chromosome 11q14 Region

Jean Weissenbach, Louis Dubertret, Judith Fischer, 1997, European journal of human genetics : EJHG.

Human Hormone-Sensitive Lipase: Genetic Mapping, Identification of a New Dinucleotide Repeat, and Association With Obesity and NIDDM

C. Fizames, J. Weissenbach, C. Dib, 1998, Diabetes.

Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2.

J. Weissenbach, J. Burgunder, J. Prud'homme, 1996, Brain : a journal of neurology.

A polymorphic DNA sequence from the terminal part of chromosome 12q [D12S37].

J. Weissenbach, A. de la Chapelle, F. Rouyer, 1990, Nucleic acids research.

Construction of a highly annotated cosmid contig spanning 550Kb within the X-linked nonspecific mental retardation candidate region at Xp21.3-22.1.

J. Weissenbach, T. Bruls, P. Marynen, 1999, American journal of medical genetics.

An isolated cardiac conduction disease maps to chromosome 19q.

J. Weissenbach, J. Loiselet, J. Demaille, 1995, Circulation research.

Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11

J. Beckmann, J. Weissenbach, C. Hengstenberg, 1993, Nature Genetics.

A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34.

J. Weissenbach, A. Durr, A. Dürr, 2000, American journal of human genetics.

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.

J. Weissenbach, K. Davies, M. Coleman, 1994, Genomics.

Autosomal recessive lamellar ichthyosis: identification of a new mutation in transglutaminase 1 and evidence for genetic heterogeneity

J. Weissenbach, J. Prud'homme, L. Dubertret, 1995 .

Regional assignment of human ESTs by whole-genome radiation hybrid mapping

G. Gyapay, J. Weissenbach, P. Goodfellow, 1996, Mammalian Genome.

Genetic and physical mapping of the progressive epilepsy with mental retardation (EPMR) locus on chromosome 8p.

J. Weissenbach, S. Leal, T. Gilliam, 1996, Genome research.

Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies

J. Weissenbach, Y. Agid, A. Brice, 1994, Neurology.

Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q

J. Weissenbach, A. Munnich, J. Melki, 1993, Nature genetics.

FISH-Mapped CEPH YACs spanning 0 to 46 cM on human chromosome 6.

J. Weissenbach, D. Paslier, P. Bray-Ward, 1996, Genomics.

Genetic linkage of Meleda disease to chromosome 8qter

C. Fizames, J. Weissenbach, R. Heilig, 1998, European Journal of Human Genetics.

Lamellar Ichthyosis: further narrowing, physical and expression mapping of the chromosome 2 candidate locus

C. Fizames, J. Weissenbach, C. Clépet, 1998, European Journal of Human Genetics.

A gene for Leber's congenital amaurosis maps to chromosome 17p

J. Weissenbach, A. Munnich, D. Bonneau, 1995 .

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

J. Weissenbach, Y. Agid, A. Vignal, 1994, Neuromuscular Disorders.

Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors.

J. F. Burrows, J. Weissenbach, P. Johnston, 2000, Cancer research.

Erratum: A radiation hybrid transcript map of the mouse genome (Nature Genetics (2001) 29 (194-200))

Patricia Rodriguez-Tomé, Hans Lehrach, Roger D. Cox, 2001 .

Physical and genetic mapping of human chromosome 3 loci containing microsatellite repeats

J. Weissenbach, N. Matsunami, Raymond White, 1994, Chromosome Research.

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)

J. Weissenbach, H. Lehrach, K. Davies, 1996, Human Genetics.

YAC/STS map across 12 Mb of Xq27 at 25-kb resolution, merging Xq26-qter.

J. Weissenbach, D. Schlessinger, S. Mumm, 1996, Genomics.

YAC/STS map of 9 Mb of Xq26 at 100-kb resolution, localizing 6 ESTs, 6 genes, and 32 genetic markers.

J. Weissenbach, D. Schlessinger, S. Mumm, 1996, Genomics.

Clinical and Genetic Heterogeneity of Leber’s Congenital Amaurosis

J. Weissenbach, A. Munnich, A. Vignal, 1993 .

Fine mapping of the cystinosis gene using an integrated genetic and physical map of a region within human chromosome band 17p13.

D. Ledbetter, M. Polymeropoulos, J. Weissenbach, 1996, Biochemical and molecular medicine.

The role of SOX9 in autosomal sex reversal and campomelic dysplasia.

J. Weissenbach, J. W. Foster, P. Goodfellow, 1995, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

Pycnodysostosis: refined linkage and radiation hybrid analyses reduce the critical region to 2 cM at 1q21 and map two candidate genes

J. Weissenbach, B. Gelb, R. Desnick, 1996, Human Genetics.

Yeast artificial chromosome and radiation hybrid map of loci in chromosome band 8p22, a common region of allelic loss in multiple human cancers.

J. Weissenbach, P. O'Connell, R. Bookstein, 1994, Genomics.

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC).

K H Buetow, J C Murray, J. Weber, 1994, Science.

A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21

J. Weissenbach, J. Prud'homme, A. Dürr, 2007, Neurology.

Refined genetic mapping of X-linked thoracoabdominal syndrome.

J. Weissenbach, R. Carmi, S. Mumm, 1996, American journal of medical genetics.

Strong linkage disequilibrium and haplotype analysis in Japanese pedigrees with Machado-Joseph disease.

J. Weber, J. Weissenbach, S. Tsuji, 1996, American journal of medical genetics.

Fine structure mapping of the human X-linked hypophosphatemic rickets gene locus.

J. Weissenbach, F. Francis, D. Barker, 1994, The Journal of clinical endocrinology and metabolism.

A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene.

E. Haan, J. Weissenbach, D. Paslier, 1994, Human molecular genetics.

Report of the First International Workshop on Human Chromosome 20 Mapping 1993

J. Weissenbach, T. Keith, I. Hansmann, 1994 .

Physical localization of microsatellite markers at the ataxia-telangiectasia locus at 11q22-q23.

M. James, J. Weissenbach, F. Collins, 1994, Genomics.

Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease.

J. Weissenbach, K. Kidd, R. Sherrington, 1995, Human molecular genetics.

Karyotype and chromosome location of characteristic tandem repeats in the pufferfish Tetraodon nigroviridis

J. Weissenbach, J. Weissenbach, H. R. Crollius, 2000, Cytogenetic and Genome Research.

Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome gene.

J. Weissenbach, V. Biancalana, E. Trivier, 1994, Genomics.

Refined mapping of a gene (NPH1) causing familial juvenile nephronophthisis and evidence for genetic heterogeneity.

J. Beckmann, J. Weissenbach, D. Paslier, 1994, Genomics.

Genetic Heterogeneity ofFamilial Hemiplegic Migraine

J. Weissenbach, J. Maziaceck, 1994 .

Human genetic map. Genome maps V. Wall chart.

J. Weber, V. Sheffield, G. Gyapay, 1994, Science.

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

J. F. Burrows, J. Weissenbach, P. Johnston, 2000 .

Isolation and Mapping of a Human SeptinGene to a Region on Chromosome 17q, Commonly Deleted in Sporadic Epithelial Ovarian Tumors

J. F. Burrows, J. Weissenbach, E. Petty, 2000 .

A new approach using multiplex long accurate PCR and yeast artificial chromosomes for bacterial chromosome mapping and sequencing.

J. Weissenbach, S. Ehrlich, S. Leal, 1996, Genome research.

A 11 Mb YAC-based contig spanning the familial juvenile nephronophthisis region (NPH1) located on chromosome 2q.

J. Weissenbach, D. Le Paslier, F. Silbermann, 1995, Genomics.