C. Jeanpierre

E. Bongers, R. Salomon, C. Antignac, 2011, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

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

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

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

Craig S. Wong, E. Zackai, H. Hakonarson, 2017, The New England journal of medicine.

Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19.

A. Hoischen, R. Pfundt, J. Veltman, 2011, American journal of human genetics.

WT1-Associated Disorders

M. Gubler, C. Jeanpierre, 2003 .

WNT/β‐catenin pathway activation in Wilms tumors: A unifying mechanism with multiple entries?

Gudrun Schleiermacher, Liliane Boccon-Gibod, Aurélien de Reyniès, 2009, Genes, chromosomes & cancer.

Molecular cytogenetic anomalies and phenotype alterations in a newly established cell line from Wilms tumor with diffuse anaplasia.

J. Gogusev, M. Faussillon, C. Jeanpierre, 2008, Cancer genetics and cytogenetics.

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

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

Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract.

R. Salomon, C. Antignac, S. Saunier, 2017, Journal of the American Society of Nephrology : JASN.

Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT)

M. Klintschar, A. Kispert, D. Haffner, 2015, Human Genetics.

RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects

R. Salomon, C. Antignac, P. Nitschké, 2011, Journal of Medical 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.

Human IFT52 mutations uncover a novel role for the protein in microtubule dynamics and centrosome cohesion.

P. Shannon, D. Chitayat, S. Saunier, 2019, Human molecular genetics.

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

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

Loss‐of‐function mutations in KIF14 cause severe microcephaly and kidney development defects in humans and zebrafish

S. Saunier, J. Roume, C. Jeanpierre, 2018, Human molecular genetics.

Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice.

F. Silbermann, S. Saunier, C. Bole-Feysot, 2017, American journal of human genetics.

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

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

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

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

DCDC2 Mutations Cause Neonatal Sclerosing Cholangitis

S. Saunier, C. Bole-Feysot, P. Nitschké, 2016, Human mutation.

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

Christophe Béroud, Claudine Junien, Cécile Jeanpierre, 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.

Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

H. Fuchs, A. Köttgen, T. Meitinger, 2023, medRxiv.

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.

Targeted next‐generation sequencing in a large series of fetuses with severe renal diseases

S. Saunier, C. Bénéteau, C. Jeanpierre, 2022, Human mutation.

The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies.

K. Tory, A. Burgun, R. Salomon, 2023, Kidney international.

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.

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

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

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

R. Berger, B. Olsen, A. Bernheim, 1988, Genomics.

Human IFT52 mutations uncover a novel role for the protein in microtubule dynamics 1 and centrosome cohesion 2

S. Saunier, C. Jeanpierre, M. Garfa-Traoré, 2020 .

Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

Nurit Assia Batzir, H. Fuchs, A. Köttgen, 2023, Kidney international.