World's Best Scientists 2026 revealed!

D-Index & Metrics

Medicine

D-Index
92
Citations
28586
World Ranking
11390
National Ranking
351

Overview

Paul Czernichow is affiliated with Grenoble Alpes University in France. The primary fields of study in their research are Medicine and Biochemistry, Genetics and Molecular Biology. Their subfields include Molecular Biology, Surgery, Neurology, Genetics, and Cellular and Molecular Neuroscience.

The research topics they have addressed span several areas, with significant work in pancreatic function and diabetes, Parkinson's disease mechanisms and treatments, diabetes and associated disorders, RNA modifications and cancer, genetics and neurodevelopmental disorders, diabetes management and research, and nuclear receptors and signaling.

Recent papers authored or co-authored by Paul Czernichow include:

  • Patient-Derived Midbrain Organoids to Explore the Molecular Basis of Parkinson's Disease, 2020, Frontiers in Neurology
  • The HASTER lncRNA promoter is a cis-acting transcriptional stabilizer of HNF1A, 2022, Nature Cell Biology
  • Regulated expression and function of the GABAB receptor in human pancreatic beta cell line and islets, 2020, Scientific Reports
  • EndoC-βH5 cells are storable and ready-to-use human pancreatic beta cells with physiological insulin secretion, 2023, Molecular Metabolism
  • The Amyotrophic Lateral Sclerosis M114T PFN1 Mutation Deregulates Alternative Autophagy Pathways and Mitochondrial Homeostasis, 2022, International Journal of Molecular Sciences

Paul Czernichow's frequent co-authors include Benjamin Galet, Javier García-Hurtado, Jorge Ferrer, M.A. Maestro, and Raphaël Scharfmann.

The venues where Paul Czernichow commonly publishes are bioRxiv (Cold Spring Harbor Laboratory), Molecular Metabolism, Frontiers in Neurology, Nature Cell Biology, and Scientific Reports.

Best Publications

  • Management of the Child Born Small for Gestational Age through to Adulthood: A Consensus Statement of the International Societies of Pediatric Endocrinology and the Growth Hormone Research Society

    P. E. Clayton;S. Cianfarani;P. Czernichow;G. Johannsson

  • Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.

    Jocelyne Magré;Marc Delépine;Eliane Khallouf;Tobias Gedde-Dahl

  • International Small for Gestational Age Advisory Board consensus development conference statement: management of short children born small for gestational age, April 24-October 1, 2001

    Peter A. Lee;Steven D. Chernausek;Anita C. S. Hokken-Koelega;Paul Czernichow

  • Activating Mutations in the ABCC8 Gene in Neonatal Diabetes Mellitus

    Andrey P. Babenko;Michel Polak;Hélène Cavé;Kanetee Busiah

  • A genetically engineered human pancreatic β cell line exhibiting glucose-inducible insulin secretion

    Philippe Ravassard;Yasmine Hazhouz;Séverine Pechberty;Emilie Bricout-Neveu

  • Small for Gestational Age: Short Stature and Beyond

    Paul Saenger;Paul Czernichow;Ieuan Hughes;Edward O. Reiter

  • Fgf10 is essential for maintaining the proliferative capacity of epithelial progenitor cells during early pancreatic organogenesis

    Anil Bhushan;Nobuyuki Itoh;Shigeaki Kato;Jean P. Thiery

  • Reduced final height and indications for insulin resistance in 20 year olds born small for gestational age: regional cohort study

    Juliane Leger;Claire Levy-Marchal;Juliette Bloch;Agnes Pinet

  • Insulin resistance early in adulthood in subjects born with intrauterine growth retardation.

    D. Jaquet;A. Gaboriau;P. Czernichow;C. Levy-Marchal

  • In utero undernutrition impairs rat beta-cell development

    A. Garofano;P. Czernichow;B. Bréant

  • Follistatin regulates the relative proportions of endocrine versus exocrine tissue during pancreatic development.

    F. Miralles;P. Czernichow;R. Scharfmann

  • Ontogeny of Leptin in Human Fetuses and Newborns: Effect of Intrauterine Growth Retardation on Serum Leptin Concentrations

    D. Jaquet;J. Leger;C. Levy-Marchal;J. F. Oury

  • Syndromic Short Stature in Patients with a Germline Mutation in the LIM Homeobox LHX4

    Kalotina Machinis;Jacques Pantel;Irène Netchine;Juliane Léger

  • Management of Graves’ Disease during Pregnancy: The Key Role of Fetal Thyroid Gland Monitoring

    Dominique Luton;Isabelle Le Gac;Edith Vuillard;Mireille Castanet

  • Beta-cell mass and proliferation following late fetal and early postnatal malnutrition in the rat.

    A. Garofano;P. Czernichow;B. Bréant

  • Nineteen Years of National Screening for Congenital Hypothyroidism: Familial Cases with Thyroid Dysgenesis Suggest the Involvement of Genetic Factors

    Mireille Castanet;Michel Polak;Catherine Bonaïti-Pellié;Stanislas Lyonnet

  • PAX8, TITF1, and FOXE1 gene expression patterns during human development: new insights into human thyroid development and thyroid dysgenesis-associated malformations.

    Sylvia Sura Trueba;Joëlle Augé;Géraldine Mattei;Heather Etchevers

  • Evaluation of Gonadal Function in 107 Intersex Patients by Means of Serum Antimüllerian Hormone Measurement

    Rodolfo A. Rey;Corinne Belville;Claire Nihoul-Fékété;Laurence Michel-Calemard

  • School Difficulties in 20-Year-Olds Who Were Born Small for Gestational Age at Term in a Regional Cohort Study

    Béatrice Larroque;Sandrine Bertrais;Paul Czernichow;Juliane Léger

  • Signaling through fibroblast growth factor receptor 2b plays a key role in the development of the exocrine pancreas

    Francisco Miralles;Paul Czernichow;Keiichi Ozaki;Nobuyuki Itoh

Frequent Co-Authors

Raphael Scharfmann
Raphael Scharfmann Université Paris Cité
Raja Brauner
Raja Brauner Université Paris Cité
Philippe Ravassard
Philippe Ravassard Université Paris Cité
Philippe Froguel
Philippe Froguel Imperial College London
Corinne Alberti
Corinne Alberti Inserm : Institut national de la santé et de la recherche médicale
Bo Ahrén
Bo Ahrén Lund University
Michael B. Ranke
Michael B. Ranke University of Tübingen
Hélène Cavé
Hélène Cavé Université Paris Cité
Stanislas Lyonnet
Stanislas Lyonnet Université Paris Cité

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