Concepedia

Author

Aurélio Balsalobre

Montreal Clinical Research InstituteORCID

Also Known As

A Balsalobre, Aurelio Balsalobre, Aurélio Balsalobre, Aurélio Balsalobre

34

Publications

6.2K

Citations

21

H-Index

47

Concepts

All Affiliations

Montreal Clinical Research InstituteMcGill UniversityUniversité de MontréalCentre National de la Recherche ScientifiqueUniversity of Geneva
AB

About

Aurélio Balsalobre is an author at Montreal Clinical Research Institute specializing in medicine, cell biology, and gene expression.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

10

10

4.9K

2

Cell Biology

9

9

4.8K

3

Health Sciences

2

2

1.9K

4

Natural Sciences

1

1

195

5

Cellular Physiology

1

1

482

Aurélio Balsalobre

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23

Publications

5.6K

Citations

20

H-Index

YearCitations

A Serum Shock Induces Circadian Gene Expression in Mammalian Tissue Culture Cells

Aurélio Balsalobre, Francesca Damiola, Ueli Schibler

Cell

1998

2K

Resetting of Circadian Time in Peripheral Tissues by Glucocorticoid Signaling

Aurélio Balsalobre, Steven A. Brown, Lysiane Marcacci,

Science

2000

1.8K

Multiple signaling pathways elicit circadian gene expression in cultured Rat-1 fibroblasts

Aurélio Balsalobre, Lysiane Marcacci, Ueli Schibler

Current Biology

2000

482

The Stat3/GR Interaction Code: Predictive Value of Direct/Indirect DNA Recruitment for Transcription Outcome

David Langlais, Catherine Couture, Aurélio Balsalobre,

Molecular Cell

2012

195

Pioneer factor Pax7 deploys a stable enhancer repertoire for specification of cell fate

Alexandre Mayran, Konstantin Khetchoumian, Fadi Hariri,

Nature Genetics

2018

173

The selector gene Pax7 dictates alternate pituitary cell fates through its pioneer action on chromatin remodeling

Lionel Budry, Aurélio Balsalobre, Konstantin Khetchoumian,

Genes & Development

2012

149

Pioneer and nonpioneer factor cooperation drives lineage specific chromatin opening

Alexandre Mayran, Kevin Sochodolsky, Konstantin Khetchoumian,

Nature Communications

2019

132

Mutations in NFKB2and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies

Thierry Brue, Marie-Hélène Quentien, Konstantin Khetchoumian,

BMC Medical Genetics

2014

93

Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing’s disease

Laura C. Hernández‐Ramírez, Ryhem Gam, Nuria Valdés,

Endocrine Related Cancer

2017

84

The<i>Cables1</i>Gene in Glucocorticoid Regulation of Pituitary Corticotrope Growth and Cushing Disease

Audrey Roussel-Gervais, Catherine Couture, David Langlais,

The Journal of Clinical Endocrinology & Metabolism

2015

64

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