Justine Bouilly

Lausanne, VD, Switzerland

Last Updated: 09/26/2026

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Found 14 publications

Nodal cytotoxic peripheral T-cell lymphoma occurs frequently in the clinical setting of immunodysregulation and is associated with recurrent epigenetic alterations.

Nodal cytotoxic peripheral T-cell lymphoma occurs frequently in the clinical setting of immunodysregulation and is associated with recurrent epigenetic alterations.

Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc

Published: October 04, 2021

Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma in Asia Frequently Shows SETD2 Alterations.

Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma in Asia Frequently Shows SETD2 Alterations.

Journal: Cancers

Published: October 22, 2020

CD73 expression in normal, hyperplastic, and neoplastic thyroid: a systematic evaluation revealing CD73 overexpression as a feature of papillary carcinomas.

CD73 expression in normal, hyperplastic, and neoplastic thyroid: a systematic evaluation revealing CD73 overexpression as a feature of papillary carcinomas.

Journal: Virchows Archiv : an international journal of pathology

Published: August 07, 2020

Primary hepatic marginal B cell lymphoma of mucosa-associated lymphoid tissue (MALT) and non-alcoholic steatohepatitis (NASH): more than a coincidence?

Primary hepatic marginal B cell lymphoma of mucosa-associated lymphoid tissue (MALT) and non-alcoholic steatohepatitis (NASH): more than a coincidence?

Journal: Annals of hematology

Published: August 15, 2018

DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development.

DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development.

Journal: Human molecular genetics

Published: September 14, 2017

KLB, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism.

KLB, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism.

Journal: EMBO molecular medicine

Published: July 30, 2017

R-spondin2, a novel target of NOBOX: identification of variants in a cohort of women with primary ovarian insufficiency.

R-spondin2, a novel target of NOBOX: identification of variants in a cohort of women with primary ovarian insufficiency.

Journal: Journal of ovarian research

Published: March 02, 2017

Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency.

Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency.

Journal: The Journal of clinical endocrinology and metabolism

Published: September 08, 2016

Impaired protein stability and nuclear localization of NOBOX variants associated with premature ovarian insufficiency.

Impaired protein stability and nuclear localization of NOBOX variants associated with premature ovarian insufficiency.

Journal: Human molecular genetics

Published: July 14, 2016

The Tyrosine Kinase Inhibitor Sunitinib Affects Ovulation but Not Ovarian Reserve in Mouse: A Preclinical Study.

The Tyrosine Kinase Inhibitor Sunitinib Affects Ovulation but Not Ovarian Reserve in Mouse: A Preclinical Study.

Journal: PloS one

Published: December 10, 2015

Germline Prolactin Receptor Mutation Is Not a Major Cause of Sporadic Prolactinoma in Humans.

Germline Prolactin Receptor Mutation Is Not a Major Cause of Sporadic Prolactinoma in Humans.

Journal: Neuroendocrinology

Published: June 04, 2015

New NOBOX mutations identified in a large cohort of women with primary ovarian insufficiency decrease KIT-L expression.

New NOBOX mutations identified in a large cohort of women with primary ovarian insufficiency decrease KIT-L expression.

Journal: The Journal of clinical endocrinology and metabolism

Published: December 17, 2014

Showing 1-12 of 14

Last Updated: 09/26/2026