J. Pantel

发表

NF1 gene analysis focused on CpG‐rich exons in a cohort of 93 patients with neurofibromatosis type 1

D. Vidaud, E. G. Boulandet, J. Pantel, 2000, Human mutation.

A genome-wide association study of anorexia nervosa

I. Ntalla, E. Zeggini, D. Pinto, 2011, Molecular Psychiatry.

Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation

Hunna J. Watson, I. Ntalla, E. Zeggini, 2018, bioRxiv.

Targeting the cis‐dimerization of LINGO‐1 with low MW compounds affects its downstream signalling

E. Kellenberger, D. Rognan, J. Pantel, 2015, British journal of pharmacology.

Analysis of Heterogeneous βA4 Peptides in Human Cerebrospinal Fluid and Blood by a Newly Developed Sensitive Western Blot Assay*

Hans Förstl, J. Schröder, K. Beyreuther, 1996, The Journal of Biological Chemistry.

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

Hunna J. Watson, I. Ntalla, E. Zeggini, 2019, Nature Genetics.

The GhsrQ343X allele favors the storage of fat by acting on nutrient partitioning

S. Luquet, J. Pantel, F. Noble, 2020, bioRxiv.

Measurement of Plasma Free Luteinizing Hormoneβ -Subunit in Women

P. Chanson, Jacques Young, J. Bidart, 2000 .

Free luteinizing-hormone beta-subunit in normal subjects and patients with pituitary adenomas.

P. Chanson, J. Bidart, J. Pantel, 1997, The Journal of clinical endocrinology and metabolism.

Characterization of Human Lutropin Carboxyl- Terminus Isoforms.

J. Bidart, J. Pantel, D. Bellet, 1998, Endocrinology.

Characterization of a monoclonal antibody reacting with the free human luteinizing hormone β-subunit

P. Chanson, J. Bidart, J. Pantel, 1996 .

Immunochemical mapping of human lutropin: II. Characterization of two monoclonal antipeptide antibodies reacting with the native β-subunit

J. Bidart, J. Pantel, D. Bellet, 1994, Molecular and Cellular Endocrinology.

Loss of constitutive activity of the growth hormone secretagogue receptor in familial short stature.

J. Pantel, S. Amselem, Y. Le Bouc, 2006, The Journal of clinical investigation.

Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders

Hunna J. Watson, Ryan L. Collins, Dan J Stein, 2019, bioRxiv.

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

Hunna J. Watson, I. Ntalla, E. Zeggini, 2019, Nature Genetics.

Development of a high throughput screen for allosteric modulators of melanocortin-4 receptor signaling using a real time cAMP assay.

R. Cone, J. Pantel, J. Corbin, 2011, European journal of pharmacology.

Species-specific Alternative Splice Mimicry at the Growth Hormone Receptor Locus Revealed by the Lineage of Retroelements during Primate Evolution

J. Pantel, S. Amselem, P. Duquesnoy, 2000, The Journal of Biological Chemistry.

Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies

Hunna J. Watson, I. Ntalla, E. Zeggini, 2019, bioRxiv.

Subcellular Localization and Mechanisms of Nucleocytoplasmic Trafficking of Steroid Receptor Coactivator-1*

E. Milgrom, J. Pantel, C. Pichon, 2003, Journal of Biological Chemistry.

Stimulation of human trophoblast invasion by placental growth hormone.

I. Laurendeau, J. Pantel, J. Guibourdenche, 2005, Endocrinology.

Common Genetic Variation and Age of Onset of Anorexia Nervosa

Hunna J. Watson, D. Pinto, S. Scherer, 2021, Biological Psychiatry Global Open Science.

Heterozygous nonsense mutation in exon 3 of the growth hormone receptor (GHR) in severe GH insensitivity (Laron syndrome) and the issue of the origin and function of the GHRd3 isoform.

J. Pantel, S. Amselem, C. Strasburger, 2003, The Journal of clinical endocrinology and metabolism.

Molecular screening of a large cohort of Moroccan patients with congenital hypopituitarism

J. Pantel, S. Amselem, N. Collot, 2015, Clinical endocrinology.

Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4.

P. Czernichow, J. Pantel, S. Amselem, 2001, American journal of human genetics.

Alternative splicing at the MEFV locus involved in familial Mediterranean fever regulates translocation of the marenostrin/pyrin protein to the nucleus.

J. Pantel, C. Cazeneuve, S. Amselem, 2000, Human molecular genetics.

Using ancestry-informative markers to identify fine structure across 15 populations of European origin

Graham M Lord, Günter P. Wagner, I. Ntalla, 2014, European Journal of Human Genetics.

Enhanced responsiveness of Ghsr Q343X rats to ghrelin results in enhanced adiposity without increased appetite

J. Pantel, D. Geny, J. Epelbaum, 2016, Science Signaling.

Associations between ADHD and various eating disorders : A Swedish nationwide population study using multiple genetically informative approaches

Hunna J. Watson, I. Ntalla, E. Zeggini, 2019 .

Recessive isolated growth hormone deficiency and mutations in the ghrelin receptor.

J. Pantel, S. Amselem, Y. Le Bouc, 2009, The Journal of clinical endocrinology and metabolism.

Mapping of HCG-receptor complexes

R. Salesse, E. Pajot-Augy, J. Bidart, 1996, Molecular and Cellular Endocrinology.

A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

John J. Connolly, I. Ntalla, E. Zeggini, 2017, Scientific Reports.

Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches

Hunna J. Watson, I. Ntalla, E. Zeggini, 2019, Biological Psychiatry.

Genome-Wide Association Study Reveals First Locus for Anorexia Nervosa and Metabolic Correlations

Hunna J. Watson, I. Ntalla, E. Zeggini, 2016, bioRxiv.

Unmasking of an immunoreactive site on the alpha subunit of human choriogonadotropin bound to the extracellular domain of its receptor.

R. Salesse, J. Bidart, J. Pantel, 1993, Biochemical and biophysical research communications.

Molecular screening of a large cohort of Moroccan patients with congenital hypopituitarism

J. Pantel, S. Amselem, N. Collot, 2015, Clinical endocrinology.

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.

Hunna J. Watson, Sarah M. Hartz, I. Ntalla, 2020, Addiction biology.

Common Genetic Variation and Age of Onset of Anorexia Nervosa

I. Giegling, S. Djurovic, R. Ophoff, 2023 .