Juan Antonio Aguilar‐Pimentel

Helmholtz Zentrum München — Germany

Medicine · Health Sciences

29h-index3.5kcitations82works2.02yr avg
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Research Topics

Asthma and respiratory diseases(13), Adipose Tissue and Metabolism(11), Allergic Rhinitis and Sensitization(9), RNA modifications and cancer(9), RNA Research and Splicing(7)

Publications80 total

Loss of histone macroH2A1.1 causes kidney abnormalities secondary to a change in nutrient metabolization
Science Advances·2025Open Access
Abcb5-deficient mice show a subtle, pleiotropic phenotype indicating a role for this transporter in intermediary metabolism
iScience·2025Open Access
NRAC controls CD36-mediated fatty acid uptake in adipocytes and lipid clearance in vivo
The EMBO Journal·2025· 1 citedOpen Access
Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
Science Advances·2025· 3 citedOpen Access
X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomes
Nature Communications·2024· 4 citedOpen Access
Comparative Phenotyping of Mice Reveals Canonical and Noncanonical Physiological Functions of TRα and TRβ
Endocrinology·2024· 5 cited
<scp>LncRNA <i>U90926</i></scp> is dispensable for the development of obesity‐associated phenotypes in vivo
Physiological Reports·2024· 1 citedOpen Access
Comparative phenotyping of mice reveals canonical and noncanonical physiological functions of TRα and TRβ
2023· 1 citedOpen Access
Insights into energy balance dysregulation from a mouse model of methylmalonic aciduria
Human Molecular Genetics·2023· 5 citedOpen Access
AOX delays the onset of the lethal phenotype in a mouse model of Uqcrh (complex III) disease
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease·2023· 5 citedOpen Access
Knockout mouse models as a resource for the study of rare diseases
Mammalian Genome·2023· 35 citedOpen Access
Genome-wide screening reveals the genetic basis of mammalian embryonic eye development
BMC Biology·2023· 18 citedOpen Access
GPR101 loss promotes insulin resistance and diet-induced obesity risk
Neuroscience Applied·2023· 2 citedOpen Access
Deep phenotyping and lifetime trajectories reveal limited effects of longevity regulators on the aging process in C57BL/6J mice
Nature Communications·2022· 40 citedOpen Access
Identifying causal serum protein–cardiometabolic trait relationships using whole genome sequencing
Human Molecular Genetics·2022· 17 citedOpen Access
Knockout mouse models as a resource for rare diseases studies
Research Square (Research Square)·2022Open Access
Thermosensitive PLGA–PEG–PLGA Hydrogel as Depot Matrix for Allergen-Specific Immunotherapy
Pharmaceutics·2022· 16 citedOpen Access
Mice lacking the mitochondrial exonuclease MGME1 develop inflammatory kidney disease with glomerular dysfunction
PLoS Genetics·2022· 18 citedOpen Access
Dietary intervention improves health metrics and life expectancy of the genetically obese Titan mouse
Communications Biology·2022· 8 citedOpen Access
Publisher Correction: Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy
Nature Cardiovascular Research·2022· 4 citedOpen Access
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Frequent Co-authors

Martin Hrabě de Angelis(42), Helmut Fuchs(37), Valérie Gailus‐Durner(33), Birgit Rathkolb(28), Lore Becker(26), Lillian Garrett(25), Sabine M. Hölter(24), Jan Rozman(24), Dirk H. Busch(24), Markus Ollert(24), Julia Calzada‐Wack(24), Eckhard Wolf(21), Thomas Klopstock(20), Wolfgang Wurst(20), Oana V. Amarie(18), Jochen Graw(17), Thure Adler(16), Martin Klingenspor(16), Frauke Neff(15), Wolfgang Hans(14)