C. Junien

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Maternal Diets Trigger Sex-Specific Divergent Trajectories of Gene Expression and Epigenetic Systems in Mouse Placenta

A. Gabory, Laure Ferry, I. Fajardy, 2012, PloS one.

Changes in WT1 splicing are associated with a specific gene expression profile in Wilms' tumour

C. Junien, D. Baudry, M. Faussillon, 2002, Oncogene.

Mutations in PCSK9 cause autosomal dominant hypercholesterolemia

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

Chromosomal assignment of the human 2,3-bisphosphoglycerate mutase gene (BPGM) to region 7q34→7q22

C. Junien, V. Joulin, R. Rosa, 1987, Human Genetics.

Update of the UMD‐FBN1 mutation database and creation of an FBN1 polymorphism database

Gabor Matyas, Christophe Béroud, Claudine Junien, 2003, Human mutation.

UMD (Universal Mutation Database): A generic software to build and analyze locus‐specific databases

C Béroud, C Junien, C. Junien, 2000, Human mutation.

Life-Long Implications of Developmental Exposure to Environmental Stressors: New Perspectives.

F. Perera, J. Toppari, C. Junien, 2015, Endocrinology.

[DOhaD and epigenetic information: societal challenges].

C. Junien, E. Rial‐Sebbag, U. Simeoni, 2016, Medecine sciences : M/S.

Catalase determination in various etiologic forms of Wilms' tumor and gonadoblastoma.

C. Junien, G. Lenoir, M. Rethoré, 1983, Cancer genetics and cytogenetics.

Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma.

C. Junien, G. Lenoir, T. Glaser, 1989, Proceedings of the National Academy of Sciences of the United States of America.

CTG repeat instability and size variation timing in DNA repair‐deficient mice

Claudine Junien, C. Junien, R. Kanaar, 2003, The EMBO journal.

Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice

C. Junien, F. Radvanyi, M. Abitbol, 1997, Nature Genetics.

Characteristics ofIntergenerationa l Contractions oftheCTG RepeatinMyotonic Dystrophy

A. Roses, H. Smeets, C. Junien, 1994 .

The UMD‐LDLR database: additions to the software and 490 new entries to the database

Christophe Béroud, Mathilde Varret, Jean-Pierre Rabès, 2002, Human mutation.

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

D. Housman, C. Junien, D. Haber, 1991, Cell.

The Epigenetic Inheritance Hypothesis

C. Junien, 2002 .

Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11.

C. Junien, F. Brunelle, J. Saudubray, 2001, The American journal of pathology.

Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy.

C. Junien, F. Brunelle, J. Saudubray, 1997, The Journal of clinical investigation.

Regional assignment of red cell acid phosphatase locus to band 2p25

C. Junien, R. Berger, A. Bernheim, 1979, Human Genetics.

Gene dosage effect for GALT in 9p trisomy and in 9p tetrasomy with an improved technique for GALT determination

C. Junien, P. Eydoux, S. Despoisse, 2004, Human Genetics.

Prenatal diagnosis of congenital enzymopenic methaemoglobinaemia with mental retardation due to generalized cytochrome b5 reductase deficiency: First report of two cases

C. Junien, J. Kaplan, J. Boué, 1981, Prenatal diagnosis.

Glucose-6-phosphate dehydrogenase and hemoglobin variants in Kel Kummer Tuareg and related groups. Indirect evidence for alpha-thalassemia trait.

D. Labie, C. Junien, J. Kaplan, 1982, Human heredity.

Maternal obesity programs increased leptin gene expression in rat male offspring via epigenetic modifications in a depot-specific manner

J. Eeckhoute, A. Gabory, J. Lesage, 2017, Molecular metabolism.

Depot- and sex-specific effects of maternal obesity in offspring's adipose tissue.

A. Gabory, J. Lesage, D. Vieau, 2016, The Journal of endocrinology.

Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13.

C. Junien, C. Lavedan, M. Rethoré, 1989, Cytogenetics and cell genetics.

Maternal calorie restriction modulates placental mitochondrial biogenesis and bioenergetic efficiency: putative involvement in fetoplacental growth defects in rats.

A. Gabory, S. Mayeur, J. Lesage, 2013, American journal of physiology. Endocrinology and metabolism.

Generalised deficiency of cytochrome b5 reductase in congenital methaemoglobinaemia with mental retardation

C. Junien, J. Kaplan, A. Leroux, 1975, Nature.

[Prenatal diagnosis of generalized cytochrome b5 reductase deficiency (congenital methemoglobinemia with mental retardation, type II) (author's transl)].

C. Junien, J. Kaplan, J. Boué, 1981, Annales de medecine interne.

Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia

C. Junien, M. Krempf, G. Luc, 2005, Human mutation.

The distal region of 11p13 and associated genetic diseases.

C. Junien, G. Saunders, B. Williams, 1991, Genomics.

Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci.

N. Nowak, T. Shows, C. Junien, 1988, Science.

Epigenetics In Transgenerational Responses To Environmental Impacts : Facts And Gaps

A. Gabory, C. Junien, L. Pirola, 2015 .

Lukaszewski , Sophie rats putative involvement in fetoplacental growth defects in mitochondrial biogenesis and bioenergetic efficiency : Maternal calorie restriction modulates placental

A. Gabory, S. Mayeur, J. Lesage, 2012 .

Maternal environment and the reproductive function of the offspring.

C. Junien, B. Mandon-Pépin, R. Lévy, 2012, Theriogenology.

Relationships among electrophysiological findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophy.

C. Junien, A. Lazarus, J. Coste, 1999, Circulation.

Third Santorini conference pharmacogenomics workshop report: “Pharmacogenomics at the crossroads: what else than good science will be needed for the field to become part of Personalized Medicine?”

G. Siest, P. Beaune, C. Junien, 2007, Clinical chemistry and laboratory medicine.

Isolation of kidney complementary DNAs down-expressed in Wilms' tumor by a subtractive hybridization approach.

C. Junien, M. Cohen-Salmon, C. Béroud, 1993, Cancer research.

Identification of 23 TGFBR2 and 6 TGFBR1 gene mutations and genotype‐phenotype investigations in 457 patients with Marfan syndrome type I and II, Loeys‐Dietz syndrome and related disorders

C. Junien, G. Jondeau, M. Claustres, 2008, Human mutation.

Demonstration of the recurrence of Marfan-like skeletal and cardiovascular manifestations due to germline mosaicism for an FBN1 mutation.

C. Junien, G. Jondeau, G. Collod-Béroud, 1999, American Journal of Human Genetics.

Heterozygous TGFBR2 mutations in Marfan syndrome

Yusuke Nakamura, Naomichi Matsumoto, Mathilde Varret, 2004, Nature Genetics.

Beckwith-Wiedemann syndrome, tumourigenesis and imprinting.

C. Junien, 1992 .

c-Ha-ras1 is not deleted in aniridia–Wilms' tumour association

C. Junien, G. Lenoir, S. Despoisse, 1983, Nature.

(2016). Depot- and sex-specific effects of maternal obesity in offspring's adipose tissue. Journal of Endocrinology , 230 (1), 39-53.

A. Gabory, J. Lesage, D. Vieau, 2019 .

The molecular basis of familial hypercholesterolemia in Lebanon: Spectrum of LDLR mutations and role of PCSK9 as a modifier gene

A. Munnich, C. Junien, C. Boileau, 2009, Human mutation.

An oligonucleotide microarray for mouse imprinted genes profiling

A. Vigé, C. Gallou-Kabani, M. Gross, 2006, Cytogenetic and Genome Research.

Placental expression of the obesity-associated gene FTO is reduced by fetal growth restriction but not by macrosomia in rats and humans

A. Gabory, I. Fajardy, S. Mayeur, 2012, Journal of Developmental Origins of Health and Disease.

CTG Trinucleotide Repeat “Big Jumps”: Large Expansions, Small Mice

A. Munnich, C. Junien, M. Gomes-Pereira, 2007, PLoS genetics.

Nutritional epigenomics of metabolic syndrome: new perspective against the epidemic.

C. Gallou-Kabani, C. Junien, C. Gallou‐Kabani, 2005, Diabetes.

Familial ligand‐defective apolipoprotein B‐100: Simultaneous detection of the ARG3500→GLN and ARG3531→CYS mutations in a French population

C. Junien, M. Krempf, G. Jondeau, 1997, Human mutation.

[Nutritionnal epigenomics: consequences of unbalanced diets on epigenetics processes of programming during lifespan and between generations].

A. Vigé, C. Gallou-Kabani, M. Gross, 2005, Annales d'endocrinologie.

Sex in basic research: concepts in the cardiovascular field.

I. König, V. Regitz-Zagrosek, J. Erdmann, 2017, Cardiovascular research.

Molecular Spectrum of Autosomal Dominant Hypercholesterolemia in France

A. Munnich, C. Junien, C. Boileau, 2010, Human mutation.

Recurrent mutation at aa 792 in the LDL receptor gene in a French patient

C. Junien, C. Boileau, L. Monnier, 1991, Human Genetics.

Assignment of NADH-cytochrome b5 reductase (DIA1 locus) to human chromosome 22

C. Junien, D. Weil, J. Kaplan, 1978, Human Genetics.

Conservation of the human COL1A1-TK-GAA synteny and homoeologous assignment in the African green monkey and the baboon (Cercopithecoidae)

C. Junien, C. Turleau, C. Cochet, 2004, Human Genetics.

Assignment of the human pro alpha 2(I) collagen structural gene (COLIA2) to chromosome 7 by molecular hybridization.

M. Gross, C. Junien, D. Weil, 1982, American journal of human genetics.

The genes coding for A alpha-, B beta-, and gamma-chains of fibrinogen map to 4q2.

C. Junien, D. Weil, A. Kahn, 1984, American journal of human genetics.

Abstracts of workshop presentations (Part 6 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.

C. Junien, C. Boileau, L. Mouthon, 2006, Rheumatology.

Proceedings of the founding meeting of SF-DOHaD

A. Gabory, L. Jouneau, A. Vigé, 2013 .

Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma

C. Junien, A. Lamouroux, H. Journel, 1989, Human Genetics.

Molecular analysis of a reciprocal translocation t(5;11)(q11;p13) in a WAGR patient

C. Junien, J. Serre, M. Azoulay, 1988, Human Genetics.

The proα2 (V) collagen gene (COL5A2) maps to 2q14→2q32, syntenic to the proα1 (III) collagen locus (COL3A1)

K. Grzeschik, C. Junien, D. Weil, 1986, Human Genetics.

The beta chorionic gonadotropin-beta luteinizing gene cluster maps to human chromosome 19

C. Junien, D. Weil, C. Julier, 2004, Human Genetics.

The gene for human fibroblast interferon (IFB) maps to 9p21

C. Junien, C. Turleau, J. Sizun, 2004, Human Genetics.

Detection of carriers for duchenne muscular dystrophy. Quality control of creatine kinase assay

C. Junien, J. Lalouel, H. Plauchu, 1982, Human Genetics.

Screening for new mutations in the LDL receptor gene in seven French familial hypercholesterolemia families by the single strand conformation polymorphism method

C. Junien, B. Dastugue, C. Boileau, 1992, Human mutation.

Genetics of neonatal hyperinsulinism

C. Junien, B. Glaser, T. Otonkoski, 2000, Archives of disease in childhood. Fetal and neonatal edition.

Abstracts for the committee on the genetic constitution of chromosome 1

Brien, J. Beckmann, K. Kidd, 1991 .

Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor.

C. Junien, C. Béroud, C. Antignac, 1990, Genomics.

cDNA cloning, tissue distribution and chromosomal localization of the human ID4 gene.

C. Junien, M. Rigolet, E. Viégas-Péquignot, 1998, DNA research : an international journal for rapid publication of reports on genes and genomes.

" Marfan syndrome " to " a Marfan-like disorder

C. Junien, G. Jondeau, C. Boileau, 2007 .

Myotonic dystrophy: size- and sex-dependent dynamics of CTG meiotic instability, and somatic mosaicism.

C. Junien, C. Lavedan, Johnson, 1993, American journal of human genetics.

Abstracts of workshop presentations (Part 2 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

Loss of Imprinted Genes and Paternal SUR1 Mutations Lead to Focal Form of Congenital Hyperinsulinism

C. Junien, F. Brunelle, J. Saudubray, 2000, Hormone Research in Paediatrics.

Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasia.

C. Junien, F. Brunelle, J. Saudubray, 1998, Annales d'endocrinologie.

Facial appearance in persistent hyperinsulinemic hypoglycemia.

C. Junien, F. Brunelle, J. Saudubray, 2002, American journal of medical genetics.

Clinical features of 52 neonates with hyperinsulinism.

C. Junien, C. Sempoux, F. Brunelle, 1999, The New England journal of medicine.

Identification of the haplotype associated with the APOB‐3500 mutation in a French hypercholesterolemic subject: Further support for a unique European ancestral mutation

C. Junien, C. Boileau, P. Benlian, 1993, Human mutation.

Effect of Maternal Obesity and Preconceptional Weight Loss on Male and Female Offspring Metabolism and Olfactory Performance in Mice

N. Meunier, A. Gabory, L. Jouneau, 2019, Nutrients.

Abstracts of workshop presentations (Part 12 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

Anderson's disease: genetic exclusion of the apolipoprotein-B gene in two families.

C. Junien, I. Beucler, P. Benlian, 1991, The Journal of clinical investigation.

Multiple acral fibromas in a patient with familial retinoblastoma: a cutaneous marker of tumour‐suppressor gene germline mutation?

C. Junien, J. Guilhou, O. Dereure, 2000, The British journal of dermatology.

Placental contribution to the origins of sexual dimorphism in health and diseases: sex chromosomes and epigenetics

A. Gabory, C. Junien, L. Moore, 2013, Biology of Sex Differences.

S4-2: Sex-specific increased resistance to diet induced obesity in offspring of obese & diabetic mothers fed a control diet during gestation: Transcriptional and epigenetic signatures associated with peripheral leptin-resistance

A. Gabory, L. Jouneau, L. Attig, 2013 .

HLA-DRB1 and DQB1 genotypes in patients with insulin-dependent neonatal diabetes mellitus. A study of 13 cases.

C. Junien, C. Bouvattier, J. Robert, 2000, Tissue antigens.

Variable features of transient neonatal diabetes mellitus with paternal isodisomy of chromosome 6

C. Junien, C. Benezech, C. Diatloff-Zito, 2000, European Journal of Human Genetics.

Identification of 23 TGFBR 2 and 6 TGFBR 1 gene mutations and genotype-phenotype investigations in 457 patients with Marfan syndrome type I and II , Loeys-Dietz syndrome and related disorders

C. Junien, G. Jondeau, M. Claustres, 2019 .

Mutations and polymorphisms in the proprotein convertase subtilisin kexin 9 (PCSK9) gene in cholesterol metabolism and disease

A. Munnich, C. Junien, C. Boileau, 2009, Human mutation.

The focal form of persistent hyperinsulinemic hypoglycemia of infancy: morphological and molecular studies show structural and functional differences with insulinoma.

C. Junien, C. Sempoux, K. Dahan, 2003, Diabetes.

A simple and fast method for cell recovery and DNA content analysis from various mouse tissues by flow cytometry

C. Junien, G. Gourdon, J. Mégret, 2007, Cytotechnology.

Misdiagnosed normal fetus owing to undetected germinal mosaicism for DMD deletion.

C. Junien, C. Boileau, 1989, Journal of medical genetics.

Cancer nutrigenomics.

C. Junien, C. Gallou, 2004, World review of nutrition and dietetics.

The human MyoDl ( MYF 3 ) gene maps on the short arm of chromosome 11 but is not associated with the W AGR locus or the region for the Beckwith-Wiedemann syndrome

T. Braun, C. Junien, M. Gessler, 2011 .

Single base pair germ-line deletion in the p53 gene in a cancer predisposed family

C. Junien, G. Thomas, R. Hamelin, 1994, Human Genetics.

The human MyoD1 (MYF3) gene maps on the short arm of chromosome 11 but is not associated with the WAGR locus or the region for the Beckwith-Wiedemann syndrome

T. Braun, H. Arnold, C. Junien, 1990, Human Genetics.

Report of the committee on chromosome and gene loss in human neoplasia

C. Junien, M. L. Beau, S. Naylor, 1991 .

Abstracts of workshop presentations pp. 1106-1116

R. L. Miller, D. Cox, D. Ledbetter, 1989 .

Isolation and Characterization of the Human Fibrillar Collagen Genes a

C. Junien, D. Weil, M. Bernard, 1985, Annals of the New York Academy of Sciences.

Abstracts of workshop presentations (Part 10 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

WT1 splicing alterations in Wilms' tumors.

C. Junien, D. Baudry, M. Cabanis, 2000, Clinical cancer research : an official journal of the American Association for Cancer Research.

WT 1 Splicing Alterations in Wilms ’ Tumors 1

C. Junien, D. Baudry, M. Cabanis, 2000 .

Mapping of a human fibrillar collagen gene, pro α1(XI) (COL11A1), to the p21 region of chromosome 1

C. Junien, R. Berger, B. Olsen, 1988 .

Beckwith-Wiedemann syndrome, tumourigenesis and imprinting

C. Junien, 1992, Current Biology.

Sexual dimorphism in environmental epigenetic programming

A. Gabory, L. Attig, C. Junien, 2009, Molecular and Cellular Endocrinology.

Human type I procollagen genes are located on different chromosomes.

M. Gross, C. Junien, A. de la Chapelle, 1982, Proceedings of the National Academy of Sciences of the United States of America.

Epigenetic control of development and expression of quantitative traits.

C. Junien, P. Chavatte-Palmer, H. Jammes, 2011, Reproduction, fertility, and development.

Inverted tandem duplication of the short arm of chromosome 8: a non-random de novo structural aberration in man. Localization of the gene for glutathione reductase in subband 8p21.1.

C. Junien, A. de la Chapelle, P. K. Jensen, 1982, Annales de genetique.

Assignment of phosphoglycerate mutase (PGAMA) to human chromosome 10. Regional mapping of GOT1 and PGAMA to subbands 10q26.1 (or q25.3).

C. Junien, C. Turleau, R. Fundele, 1982, Annales de genetique.

Foetal enzyme pattern of two alveolar rhabdomyosarcomas.

C. Junien, F. Schapira, C. Micheau, 1972, Revue europeenne d'etudes cliniques et biologiques. European journal of clinical and biological research.

The organization of two related subfamilies of a human tandemly repeated DNA is chromosome specific

C. Junien, D. Weil, P. Gallano, 2004, Human Genetics.

Gene dosage effect in human triploid fibroblasts

C. Junien, J. Boué, A. Boué, 1976, Human Genetics.

Role for the Wilms tumor gene in genital development?

C. Junien, M. Gessler, W. Bickmore, 1990, Proceedings of the National Academy of Sciences of the United States of America.

[Increase of the LDH-B activity in a boy with 12p trisomy by malsegregation of a maternal translocation t(12;14) (q12;p11)].

C. Junien, B. Dutrillaux, A. Aurias, 1975, Annales de genetique.

Abstracts for the committee on the genetic constitution of the X chromosome (Part 3 of 3)

Brien, J. Beckmann, K. Kidd, 1991 .

Child health, developmental plasticity, and epigenetic programming.

M. Fraga, C. Junien, R. Scharfmann, 2011, Endocrine reviews.

Metabolic imprinting, programming and epigenetics – a review of present priorities and future opportunities

S. Lewis, C. Junien, B. Koletzko, 2010, British Journal of Nutrition.

Further evidence for the dispersion of the human fibrillar collagen genes.

K. Grzeschik, C. Junien, D. Weil, 1986, American journal of human genetics.

Frequent overexpression of cyclin D2/cyclin-dependent kinase 4 in Wilms' tumor.

C. Junien, M. Faussillon, C. Jeanpierre, 2005, Cancer letters.

Parental Imprinting of Human Chromosome Region 11p15.3-pter Involved in the Beckwith-Wiedemann Syndrome and Various Human Neoplasia

A. Feinberg, R. Weksberg, N. Niikawa, 1994, European journal of human genetics : EJHG.

The Genetics of Neonatal Hyperinsulinism

C. Junien, J. Fournet, 2003, Hormone Research in Paediatrics.

Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia.

C. Junien, F. Brunelle, J. Saudubray, 1998, The Journal of clinical investigation.

Developmental programming and epigenetics.

A. Gabory, L. Attig, C. Junien, 2011, The American journal of clinical nutrition.

Placental contribution to nutritional programming of health and diseases: epigenetics and sexual dimorphism

A. Gabory, C. Junien, A. Tarrade, 2015, Journal of Experimental Biology.

CpG islands surround a DNA segment located between translocation breakpoints associated with genitourinary dysplasia and aniridia.

C. Junien, D. Porteous, W. Bickmore, 1989, Genomics.

Diagnosis of Duchenne and Becker muscular dystrophies by polymerase chain reaction. A multicenter study.

D. Bentley, A. Covone, C. Junien, 1992, JAMA.

Sex- and Diet-Specific Changes of Imprinted Gene Expression and DNA Methylation in Mouse Placenta under a High-Fat Diet

A. Gabory, A. Vigé, S. Mayeur, 2010, PloS one.

2 Implications for Obesity and Common Diseases

A. Vigé, C. Gallou-Kabani, M. Gross, 2007 .

Sexual dimorphism 24 / 02 / 09 1 Sexual Dimorphism in Environmental Epigenetic Programming

A. Gabory, L. Attig, C. Junien, 2018 .

Sexual Dimorphism and DOHaD through the Lens of Epigenetics: Genetic, Ancestral, Developmental, and Environmental Origins from Previous to the Next Generation(s)

A. Gabory, C. Junien, S. Voisin, 2016 .

Conference on ‘ Over-and undernutrition : challenges and approaches ’ Symposium 2 : Modern approaches to nutritional research challenges Nutritional developmental epigenomics : immediate and long-lasting effects

A. Gabory, L. Attig, C. Junien, 2010 .

C57BL/6J and A/J Mice Fed a High‐Fat Diet Delineate Components of Metabolic Syndrome

A. Vigé, C. Gallou-Kabani, M. Gross, 2007, Obesity.

Mutations of the VHL gene in sporadic renal cell carcinoma: Definition of a risk factor for VHL patients to develop an RCC

C. Junien, S. Richard, C. Béroud, 1999, Human mutation.

Software and database for the analysis of mutations in the VHL gene

Christophe Béroud, Claudine Junien, Dominique Joly, 1998, Nucleic Acids Res..

Epigenetic mechanisms involved in developmental nutritional programming.

A. Gabory, L. Attig, C. Junien, 2011, World journal of diabetes.

Developmental programming and epigenetics 1 – 4

A. Gabory, L. Attig, C. Junien, 2011 .

Early nutrition and epigenetic programming: chasing shadows

A. Gabory, L. Attig, C. Junien, 2010, Current opinion in clinical nutrition and metabolic care.

Autosomal dominant type IIa hypercholesterolemia: evaluation of the respective contributions of LDLR and APOB gene defects as well as a third major group of defects

C. Junien, M. Krempf, C. Bonaïti‐pellié, 2000, European Journal of Human Genetics.

Genetics of Wilms' tumor: a blend of aberrant development and genomic imprinting.

C. Junien, I. Henry, 1994, Kidney international.

Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith–Wiedemann syndrome

C. Junien, W. Reik, V. D. Der Kaloustian, 2003, Journal of medical genetics.

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

C. Junien, C. Schwartz, C. Bonaïti‐pellié, 1991, Nature.

Wiedman-Beckwith syndrome, tumorigenesis and imprinting.

C. Junien, 1996, Acta geneticae medicae et gemellologiae.

Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females.

C Junien, C. Junien, C. Bonaïti‐pellié, 1992, Journal of medical genetics.

Somatic Mosaicism for Partial Paternal Isodisomy in Wiedemann-Beckwith Syndrome: A Post-Fertilization Event

C. Junien, P. Landrieu, M. Mannens, 1993, European journal of human genetics : EJHG.

Congenital hyperinsulinism and mosaic abnormalities of the ploidy

C. Junien, C. Sempoux, F. Brunelle, 2005, Journal of Medical Genetics.

A deletion map of the WAGR region on chromosome 11.

C. Junien, M. Gessler, G. Bruns, 1989, American journal of human genetics.

Homozygous deletion of a DNA marker from chromosome 11p13 in sporadic Wilms tumor.

H. Chan, C. Junien, L. Bonetta, 1988, Genomics.

Del 11p/aniridia complex. Report of three patients and review of 37 observations from the literature

C. Junien, C. Turleau, M. Tournade, 1984, Clinical genetics.

Physical and genetic mapping of the dipeptidase gene DPEP1 to 16q24.3.

C. Junien, C. Antignac, A. Bernheim, 1993, Genomics.

Report on the IASO Stock Conference 2006: early and lifelong environmental epigenomic programming of metabolic syndrome, obesity and type II diabetes

C. Junien, P. Nathanielsz, 2007, Obesity reviews : an official journal of the International Association for the Study of Obesity.

Molecular Basis of Epigenetic Memory

A. Vigé, C. Gallou-Kabani, M. Gross, 2007 .

Lifelong Circadian and Epigenetic Drifts in Metabolic Syndrome

A. Vigé, C. Gallou-Kabani, C. Junien, 2007, Epigenetics.

Nutri-epigenomics: lifelong remodelling of our epigenomes by nutritional and metabolic factors and beyond

A. Vigé, C. Gallou-Kabani, M. Gross, 2007, Clinical chemistry and laboratory medicine.

Defective satellite cells in congenital myotonic dystrophy.

C. Junien, G. Butler-Browne, V. Mouly, 2001, Human molecular genetics.

Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complex.

C. Junien, R. Tenconi, J. Dufier, 1980, Annales de genetique.

Beckwith-Wiedemann Syndrome, Tumorigenesis and Imprinting

C. Junien, 1992 .

Silencing of CDKN 1 C ( p 57 KIP 2 ) is associated with hypomethylation at KvDMR 1 in Beckwith – Wiedemann syndrome

C. Junien, W. Reik, E. Maher, 2003 .

Candidate genetic modifiers of individual susceptibility to renal cell carcinoma: a study of polymorphic human xenobiotic-metabolizing enzymes.

C. Junien, C. Béroud, M. Galteau, 1999, Cancer research.

[Nutritional epigenomics of metabolic syndrome].

A. Vigé, C. Gallou-Kabani, M. Gross, 2005, Medecine sciences : M/S.

MSH2-Dependent Germinal CTG Repeat Expansions Are Produced Continuously in Spermatogonia from DM1 Transgenic Mice

C. Junien, H. te Riele, G. Gourdon, 2004, Molecular and Cellular Biology.

Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability.

C. Junien, G. Gourdon, H. Hofmann-Radvanyi, 2000, Human molecular genetics.

Genetic linkage heterogeneity in myotubular myopathy.

C. Junien, J. Mandel, A. Hanauer, 1995, American journal of human genetics.

R3531C Mutation in the Apolipoprotein B Gene Is Not Sufficient to Cause Hypercholesterolemia

C. Junien, M. Krempf, C. Boileau, 2000, Arteriosclerosis, thrombosis, and vascular biology.

Blunted coronary reserve in myotonic dystrophy. An early and gene-related phenomenon.

P. Merlet, B. Mazoyer, C. Junien, 1996, Circulation.

Expression of epigenetic machinery genes is sensitive to maternal obesity and weight loss in relation to fetal growth in mice

Claudine Junien, Hélène Jammes, Luc Jouneau, 2016, Clinical Epigenetics.

Association of GSTT1 non-null and NAT1 slow/rapid genotypes with von Hippel-Lindau tumour suppressor gene transversions in sporadic renal cell carcinoma.

C. Junien, C. Béroud, D. Droz, 2001, Pharmacogenetics.

G6PD Baudelocque: a new unstable variant characterized in cultured fibroblasts.

C. Junien, J. Kaplan, A. Sender, 1974, Enzyme.

Heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Algeria

C. Junien, J. Kaplan, G. Trabuchet, 1978, Human Genetics.

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database.

E. Denamur, C. Junien, M. Gubler, 1998, American journal of human genetics.

Partial deletion of the short arm of chromosome 12(p11; p13). Report of a case.

C. Junien, F. Anglani, R. Tenconi, 1975, Annales de genetique.

Prenatal diagnosis of myotonic dystrophy using closely linked flanking markers.

C. Junien, C. Lavedan, P. Shelbourne, 1991, Journal of medical genetics.

Marfan Database (third edition): new mutations and new routines for the software

Hanns-Georg Klein, Christophe Béroud, Gwenaëlle Collod-Béroud, 1998, Nucleic Acids Res..

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.

NcoI RFLP at 19q13 identified by the DNA sequence pW119B (D19S169).

C. Junien, B. Wieringa, C. Lavedan, 1991, Nucleic acids research.

Sexual Dimorphism in Non-Mendelian Inheritance

Claudine Junien, A. Vigé, C. Gallou-Kabani, 2008, Pediatric Research.

REVIEW ARTICLE Sexual Dimorphism in Non-Mendelian Inheritance

A. Vigé, C. Gallou-Kabani, C. Junien, 2008 .

A linkage map of 10 loci flanking the Marfan syndrome locus on 15q: results of an International Consortium study.

C Junien, M Sarfarazi, P Farndon, 1992, Journal of medical genetics.

Cytogenetic forms of retinoblastoma: their incidence in a survey of 66 patients.

C. Junien, A. Leblanc, C. Turleau, 1985, Cancer genetics and cytogenetics.

Retinoblastoma, deletion 13q14, and esterase D: application of gene dosage effect to prenatal diagnosis.

C. Junien, C. Turleau, S. Despoisse, 1982, Cancer genetics and cytogenetics.

[Epigenetics, interface between environment and genes: role in complex diseases].

C. Junien, A. Scheen, 2012, Revue medicale de Liege.

Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene

Thierry Soussi, Christophe Béroud, Gwenaëlle Collod-Béroud, 1997, Nucleic Acids Res..

Seven megabase yeast artificial chromosome contig at region 11p15: identification of a yeast artificial chromosome spanning the breakpoint of a chromosomal translocation found in a case of Beckwith-Wiedemann syndrome.

C. Junien, C. Croce, S. Sabbioni, 1995, Cancer research.

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

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

Report of the committee on the genetic constitution of chromosome 11.

C. Junien, V. Heyningen, W. Mcbride, 1988, Cytogenetics and cell genetics.

Male and Female Placentas Have Divergent Transcriptomic and Epigenomic Responses to Maternal Diets: Not Just Hormones

A. Gabory, Laure Ferry, L. Jouneau, 2014 .

Dietary Alleviation of Maternal Obesity and Diabetes: Increased Resistance to Diet-Induced Obesity Transcriptional and Epigenetic Signatures

Claudine Junien, Jean-Philippe Jais, A. Gabory, 2013, PloS one.

Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis

G. Gyapay, C. Junien, C. Jeanpierre, 1995, Genes, chromosomes & cancer.

Meta‐analysis of genome‐wide DNA methylation and integrative omics of age in human skeletal muscle

S. Horvath, A. Gabory, C. Junien, 2021, Journal of cachexia, sarcopenia and muscle.

Meta-analysis of genome-wide DNA methylation and integrative OMICs in human skeletal muscle

S. Horvath, A. Gabory, C. Junien, 2020, bioRxiv.

SUBREGIONAL MAPPING OF BWS, CTSD, MYOD1, AND A T-ALL BREAKPOINT IN 11P15

C. Junien, W. Cavenee, C. Antignac, 1989 .

The isolation of genomic recombinants for the human apolipoprotein B gene and the mapping of three common DNA polymorphisms of the gene —a useful marker for human chromosome 2

S. Humphries, K. Grzeschik, C. Junien, 1986, Human Genetics.

Assignment of 112 microsatellite markers to 23 chromosome 11 subregions delineated by somatic hybrids: comparison with the genetic map.

C. Fizames, C. Junien, A. Vignal, 1994, Genomics.

Linkage analysis of five fibrillar collagen loci in a large French Marfan syndrome family.

C. Junien, G. Jondeau, C. Boileau, 1990, Journal of medical genetics.

New nomenclature and DNA testing guidelines for myotonic dystrophy type 1 (DM1)

T. Cooper, A. Roses, S. Tapscott, 2000, Neurology.

Somatic instability of the CTG repeat in mice transgenic for the myotonic dystrophy region is age dependent but not correlated to the relative intertissue transcription levels and proliferative capacities.

C. Junien, F. Radvanyi, G. Gourdon, 1998, Human molecular genetics.

Myotonic dystrophy: absence of CTG enlarged transcript in congenital forms, and low expression of the normal allele.

C. Junien, C. Lavedan, J. Rabès, 1993, Human molecular genetics.

Different sex-dependent constraints in CTG length variation as explanation for congenital myotonic dystrophy

C. Junien, J. Roume, C. Lavedan, 1993, The Lancet.

Silencing of CDKN1C ( p57 KIP2 ) is associated with hypomethylation at KvDMR1 in Beckwith–Wiedemann syndrome

C. Junien, W. Reik, N. Diaz-Meyer, 2003 .

Horizons in nutritional science : The case for strategic international alliances to harness nutritional genomics for public and personal health.

Jean-Daniel Zucker, Peter Morgan, Berthold Koletzko, 2005 .

Genotype–phenotype correlation in von Hippel‐Lindau families with renal lesions

C. Junien, S. Richard, C. Béroud, 2004, Human mutation.

Implication of the folate-methionine metabolism pathways in susceptibility to follicular lymphomas.

G. Salles, C. Junien, E. Macintyre, 2006, Blood.

Profiling of differential gene expression in Wilms tumor by cDNA expression array

C. Junien, D. Baudry, M. Faussillon, 2001, Pediatric Nephrology.

Impact of diets and nutrients/drugs on early epigenetic programming

Claudine Junien, C. Junien, 2006, Journal of Inherited Metabolic Disease.

Cadherins in Wilms' tumor: E-cadherin expression despite absence of WT1.

C. Junien, D. Baudry, M. Cabanis, 2003, Anticancer research.

Report of the committee on the genetic constitution of chromosomes 10, 11, and 12.

C. Junien, H. Kazazian, 1987, Cytogenetics and cell genetics.

A third major locus for autosomal dominant hypercholesterolemia maps to 1p34.1-p32.

C. Junien, M. Krempf, C. Boileau, 1999, American journal of human genetics.

Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndrome.

J. Mallet, C. Junien, C. Turleau, 1988, Annales de genetique.

The structural gene for lecithin:cholesterol acyl transferase (LCAT) maps to 16q22

C. Junien, D. Weil, R. Williamson, 1987, Annals of human genetics.

The structural gene for aldolase B (ALDB) maps to 9q13→32

C. Junien, D. Weil, M. Mattei, 1985, Annals of human genetics.

Msh3 is a limiting factor in the formation of intergenerational CTG expansions in DM1 transgenic mice

Claudine Junien, Laurence Hubert, C. Junien, 2006, Human Genetics.

[Molecular diagnosis of Duchenne and Becker muscular dystrophies. Current data].

C. Junien, J. Boué, A. Boué, 1987, Annales de genetique.

Software and database for the analysis of mutations in the human WT1 gene

Christophe Béroud, Claudine Junien, Cécile Jeanpierre, 1998, Nucleic Acids Res..

[Trisomy 12p caused by malsegregation of a paternal translocation t(12;22) (p11;p11)].

C. Junien, M. Rethoré, J. Kaplan, 1978, Annales de genetique.

Gene dosage effect for human triosephosphate isomerase and glyceraldehyde-3-phosphate dehydrogenase in partial trisomy 12p13 and trisomy 18p

C. Junien, J. Kaplan, A. Broustet, 1978, Human Genetics.

12pter → 12p 12.2: Possible assignment of human triose phosphate isomerase

C. Junien, J. Lejeune, M. Rethoré, 1977, Human Genetics.

PK3: A new chromosome enzyme marker for gene dosage studies in chromosome 15 imbalance

C. Junien, J. Boué, A. Boué, 2004, Human Genetics.

Report of the second chromosome 11 workshop.

C Junien, C. Junien, P. Little, 1992, Genomics.

[Localization of the gene of the glyceraldehyde 3 phosphate dehydrogenase on the distal segment of the short arm of the chromosome 12].

C. Junien, R. Tenconi, J. Lejeune, 1976, Annales de genetique.

Triplex gene dosage effect of TPI and G3PD in a human lymphoblastoid cell line with partial trisomy 12p13 and 18p

C. Junien, G. Lenoir, J. Kaplan, 1979, Human Genetics.

Duplication 15q22»15qter and its phenotypic expression

C. Junien, C. Pernot, J. Boué, 2004, Human Genetics.

Confirmation of the regional assignment of peptidase A (PEPA) to 18q23 by gene dosage studies.

C. Junien, C. Turleau, J. de Grouchy, 1980, Annales de genetique.

Direct haplotyping by double digestion of PCR-amplified creatine kinase (CKMM): application to myotonic dystrophy diagnosis.

C. Junien, R. Korneluk, C. Lavedan, 1990, Genomics.

Abstracts of workshop presentations (Part 3 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities.

A. Delacourte, C. Junien, A. Ghestem, 2001, Human molecular genetics.

[46,XX/46,XX,del (10) (p13)/47,XX,+r/47,XX,del (10) (p13), + r mosaicism and partial trisomy 10p phenotype (author's transl)].

C. Junien, J. Lejeune, M. Rethoré, 1979, Annales de genetique.

LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysis

Manfred Stuhrmann, Hartmut Schmidt, Christophe Béroud, 1998, Nucleic Acids Res..

Chromosomal assignment of the uromodulin gene (UMOD) to 16p13.11.

C. Junien, M. Cohen-Salmon, D. Callen, 1993, Cytogenetics and cell genetics.

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

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

The structural gene for transferrin (TF) maps to 3q21----3qter.

K. Grzeschik, C. Junien, D. Weil, 1984, Annales de genetique.

Genetics of neonatal hyperinsulinism

C. Junien, B. Glaser, T. Otonkoski, 2000, Archives of disease in childhood. Fetal and neonatal edition.

Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 cases

C. Junien, C. Sempoux, F. Brunelle, 2001, European Journal of Pediatrics.

Del11p13/nephroblastoma without aniridia

C. Junien, J. Dufier, C. Turleau, 2004, Human Genetics.

Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a family

C. Junien, M. Gessler, M. Mannens, 1993, Genes, chromosomes & cancer.

DM1 CTG expansions affect insulin receptor isoforms expression in various tissues of transgenic mice.

C. Junien, G. Bassez, M. Gomes-Pereira, 2007, Biochimica et biophysica acta.

Gene for apolipoprotein CII is on human chromosome 19

S. Humphries, C. Junien, D. Weil, 1984, Somatic cell and molecular genetics.

Extended Haplotypes and Linkage Disequilibrium between I I Markers at the APOA IC 3-A 4 Gene Cluster on Chromosome

C. Junien, G., J., 2006 .

Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13

C. Junien, C. Jeanpierre, F. Barichard, 1989, Human Genetics.

Identification of the first Lebanese mutation in the LPL gene and description of a rapid detection method

C. Junien, E. Chouery, C. Boileau, 2004, Clinical genetics.

Isolation and characterisation of a cDNA clone for human apolipoprotein CI and assignment of the gene to chromosome 19

S. Humphries, K. Grzeschik, C. Junien, 2004, Human Genetics.

Resistance to high-fat diet in the female progeny of obese mice fed a control diet during the periconceptual, gestation, and lactation periods.

A. Vigé, C. Gallou-Kabani, M. Gross, 2007, American journal of physiology. Endocrinology and metabolism.

[Epigenetics and Nutrition: maternal nutrition impacts on placental development and health of offspring].

A. Gabory, C. Junien, M. Lemaire, 2015, Biologie aujourd'hui.

Placental BDNF/TrkB signaling system is modulated by fetal growth disturbances in rat and human.

C Junien, A. Gabory, I. Fajardy, 2010, Placenta.

ABCC8 (SUR1) and KCNJ11 (KIR6.2) Mutations in Persistent Hyperinsulinemic Hypoglycemia of Infancy and Evaluation of Different Therapeutic Measures

M. Gross, C. Junien, F. Baş, 2002, Journal of pediatric endocrinology & metabolism : JPEM.

Genetics of congenital hyperinsulinism

C. Junien, J. Fournet, 2004, Endocrine pathology.

Major difference in aetiology and phenotypic abnormalities between transient and permanent neonatal diabetes

C. Junien, C. Bellanné-Chantelot, C. Bouvattier, 2002, Journal of medical genetics.

Strain-specific changes in nucleus accumbens transcriptome and motivation for food reward in mice exposed to maternal separation

A. Gabory, L. Jouneau, C. Junien, 2023, bioRxiv.

Myotonic dystrophy: Over-expression or/and under-expression? A critical review on a controversial point

C. Junien, H. Hofmann-Radvanyi, 1993, Neuromuscular Disorders.

Impaired cerebral glucose metabolism in myotonic dystrophy: a triplet-size dependent phenomenon

P. Merlet, D. Annane, S. Pappatà, 1998, Neuromuscular Disorders.

Correlation Between Decreased Myocardial Glucose Phosphorylation and the DNA Mutation Size in Myotonic Dystrophy

P. Merlet, D. Annane, B. Mazoyer, 1994, Circulation.

CANDIDATE GENE APPROACH TO TYPE IIa HYPERCHOLESTEROLAEMIA

C. Junien, P. Benlian, P. Douste-Blazy, 1989, The Lancet.

The gene for catalase is assigned between the antigen loci MIC4 and MIC11.

C. Junien, P. Couillin, P. Métézeau, 1989, Genomics.

Hyperinsulinemic hypoglycemia in children.

C. Junien, C. Sempoux, F. Brunelle, 2004, Annales d'endocrinologie.

Retinoblastoma-del(13q14): Report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase D

C. Junien, J. Zucker, H. Rivera, 2004, Human Genetics.

Direct gene dosage determination in patients with unbalanced chromosomal aberrations using cloned DNA sequences. Application to the regional assignment of the gene for alpha 2(I) procollagen (COLIA2).

C. Junien, M. Rethoré, C. Huerre, 1983, American journal of human genetics.

Regional assignment of arylsulfatase A, mitochondrial aconitase and NADH-cytochrome b5 reductase by somatic cell hybridization

C. Junien, J. Frézal, S. Heuertz, 2004, Human Genetics.

Two new polymorphisms in the coding sequence of the LDL receptor (LDLR) gene

C. Junien, C. Boileau, B. Saint-Jore, 1993, Human Genetics.

Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene

G Collod-Béroud, C Béroud, L Adès, 1997, Nucleic Acids Res..

Software and database for the analysis of mutations in the human LDL receptor gene

Christophe Béroud, Mathilde Varret, Jean-Pierre Rabès, 1997, Nucleic Acids Res..

Subregional physical mapping of an αB-crystallin sequence and of a new expressed sequence D11S877E to human 11q

C. Junien, O. Delattre, C. Jeanpierre, 2004, Mammalian Genome.

Report of the committee on the genetic constitution of chromosome 11.

C. Junien, V. van Heyningen, 1990, Cytogenetics and cell genetics.

[Colon cancer and nutritional genetics: modifier genes].

C. Junien, 2001, Annales de medecine interne.

Abstracts of workshop presentations pp. 1075-1091

R. L. Miller, D. Cox, D. Ledbetter, 1989 .

Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy.

C. Junien, H. Brunner, T. Ashizawa, 1994, American journal of human genetics.

A highly polymorphic probe on 11p15.5: L22.5.2 (D11S774).

C. Junien, C. Jeanpierre, A. Puech, 1991, Nucleic acids research.

Strain-specific changes in nucleus accumbens transcriptome and motivation for palatable food reward in mice exposed to maternal separation

A. Gabory, L. Jouneau, C. Junien, 2023, Frontiers in nutrition.

Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genes.

C. Junien, J. Melki, M. Babron, 1993, American journal of human genetics.

Abstracts of workshop presentations pp. 1057-1074

R. L. Miller, D. Cox, D. Ledbetter, 1989 .

Two TaqI dimorphic sites at the human beta-hydroxylase locus.

M. Leboyer, J. Mallet, A. Malafosse, 1989, Nucleic acids research.

Reply to “The question of heterogeneity in Marfan syndrome”

C. Junien, C. Bonaïti‐pellié, G. Jondeau, 1995, Nature Genetics.

Abstracts for the committee on the genetic constitution of chromosome 6

Brien, J. Beckmann, K. Kidd, 1991 .

Abstracts of workshop presentations pp. 1023-1039

R. L. Miller, D. Cox, D. Ledbetter, 1989 .

Abstracts for the committee on comparative gene mapping

Brien, J. Beckmann, K. Kidd, 1991 .

Detection of an EcoRI restriction fragment length polymorphism in the gene encoding the human TBP associated factor II 30 (TAFII30)

C. Junien, I. Henry, S. Luce, 1997, Clinical genetics.

Symposium 2: Modern approaches to nutritional research challenges Nutritional developmental epigenomics: immediate and long-lasting effects

A. Gabory, L. Attig, C. Junien, 2010 .

Reply to Gilchrist

C. Junien, G. Jondeau, C. Boileau, 1994 .

The isolation, characterisation, and chromosomal assignment of the gene for human 3-hydroxy-3-methylglutaryl coenzyme A reductase, (HMG-CoA reductase)

S. Humphries, C. Junien, R. Williamson, 2004, Human Genetics.

Abstracts for the committee on the genetic constitution of chromosome 15

Brien, J. Beckmann, K. Kidd, 1991 .

Sexual dimorphism in environmental epigenetic programming

A. Gabory, L. Attig, C. Junien, 2009, Molecular and Cellular Endocrinology.

PRENATAL DIAGNOSIS OF CONGENITAL ENZYMOPENIC METHAEMOGLOBINAEMIA WITH MENTAL RETARDATION DUE TO GENERALIZED REPORT

C. Junien, A. Leroux, D. Lostanlen, 2005 .

Mutations and polymorphisms in the proprotein convertase subtilisin kexin 9 (PCSK9) gene in cholesterol metabolism and disease

A. Munnich, C. Junien, C. Boileau, 2009, Human mutation.

Identification of 23 TGFBR2 and 6 TGFBR1 gene mutations and genotype‐phenotype investigations in 457 patients with Marfan syndrome type I and II, Loeys‐Dietz syndrome and related disorders

C. Junien, G. Jondeau, M. Claustres, 2008, Human mutation.

Software and database for the analysis of mutations in the human LDL receptor gene

C. Junien, C. Béroud, G. Collod-Béroud, 1997, Nucleic Acids Res..

Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene

C. Junien, D. Milewicz, C. Béroud, 1997, Nucleic Acids Res..