Citation Impact
Citing Papers
Hyperplasia and Carcinomas in Pten-Deficient Mice and Reduced PTEN Protein in Human Bladder Cancer Patients
2006 StandoutNobel
Alpha-B Crystallin Gene (CRYAB) Mutation Causes Dominant Congenital Posterior Polar Cataract in Humans
2001
Classic serotonergic psychedelics for mood and depressive symptoms: a meta-analysis of mood disorder patients and healthy participants
2021 Standout
CRYBA3/A1 Gene Mutation Associated with Suture-Sparing Autosomal Dominant Congenital Nuclear Cataract: A Novel Phenotype
2004
Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome
1997 Standout
Autonomic, Neuroendocrine, and Immunological Effects of Ayahuasca
2011
Structural and Functional Diversity of Connexin Genes in the Mouse and Human Genome
2002 Standout
When brain clocks lose track of time: cause or consequence of neuropsychiatric disorders
2011 StandoutNobel
Psychedelics
2016 Standout
Inherited PAX6, NF1 and OTX2 mutations in a child with microphthalmia and aniridia
2007 StandoutNobel
Evaluation of the skin sensitizing potential of biodegradable magnesium alloys
2007
WHO-EORTC classification for cutaneous lymphomas
2005 Standout
Serotonergic innervation of the amygdala: targets, receptors, and implications for stress and anxiety
2013
A deletion mutation in the ?A1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family
2004
Genetics of childhood cataract
2004
Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataract
2004
The genetics of childhood cataract
2000
Papillomaviruses and cancer: from basic studies to clinical application
2002 StandoutNobel
Characterization of a Mutation in the Lens-specific MP70 Encoding Gene of the Mouse Leading to a Dominant Cataract
2001
Reticulohistiocytoma of the dorsum
1988
Neurochemically defined cell types in the claustrum of the cat
2007
PTEN hamartoma tumor syndromes
2008 Standout
A role for the circadian genes in drug addiction
2008
HPV6b virus like particles are potent immunogens without adjuvant in man
2000
Link between a novel human gammaD-crystallin allele and a unique cataract phenotype explained by protein crystallography
2000
Connexin46 Mutations in Autosomal Dominant Congenital Cataract
1999
Crystallin γB-I4F Mutant Protein Binds to α-Crystallin and Affects Lens Transparency
2005 StandoutNobel
A Temperature-sensitive Mutation of Crygs in the Murine Opj Cataract
2001
Sexually transmitted diseases treatment guidelines
2003 Standout
The genetic and molecular basis of congenital eye defects
2003
A Nonsense Mutation in CRYBB1 Associated with Autosomal Dominant Cataract Linked to Human Chromosome 22q
2002
Cell death triggered by a novel mutation in the alphaA-crystallin gene underlies autosomal dominant cataract linked to chromosome 21q
2003
External Genital Warts: Diagnosis, Treatment, and Prevention
2002
The γ-Crystallins and Human Cataracts: A Puzzle Made Clearer
1999
The TSC1-2 tumor suppressor controls insulin–PI3K signaling via regulation of IRS proteins
2004 Standout
Quadrivalent Vaccine against Human Papillomavirus to Prevent High-Grade Cervical Lesions
2007 Standout
A new betaA1-crystallin splice junction mutation in autosomal dominant cataract.
2000
Genetic and Allelic Heterogeneity ofCrygMutations in Eight Distinct Forms of Dominant Cataract in the Mouse
2004
Development of a microstructural grand potential-based sintering model
2019
Gene expression changes during cataract progression in Sparc null mice: differential regulation of mouse globins in the lens.
2004 StandoutNobel
Past, present, and future of soft magnetic composites
2018 Standout
Degradable biomaterials based on magnesium corrosion
2008 Standout
Binder jet 3D printing—Process parameters, materials, properties, modeling, and challenges
2020 Standout
A missense mutation in the gammaD crystallin gene (CRYGD) associated with autosomal dominant "coral-like" cataract linked to chromosome 2q.
2004
EORTC classification for primary cutaneous lymphomas: a proposal from the Cutaneous Lymphoma Study Group of the European Organization for Research and Treatment of Cancer.
1997 Standout
Effect of iron particle size and volume fraction on the magnetic properties of Fe/silicate glass soft magnetic composites
2014
The Cowden syndrome: a clinical and genetic study in 21 patients
1986
Aey2, a new mutation in the betaB2-crystallin-encoding gene of the mouse.
2001
Cowden disease: gene marker studies and measurements of epidermal growth factor.
1986
The phosphatidylinositol‐3 kinase pathway regulates bladder cancer cell invasion
2003
A novel missense mutation in the gene for gap-junction protein alpha3 (GJA3) associated with autosomal dominant "nuclear punctate" cataracts linked to chromosome 13q.
2004
Expression profiling and gene discovery in the mouse lens.
2003 StandoutNobel
A novel connexin46 (GJA3) mutation in autosomal dominant congenital nuclear pulverulent cataract.
2004
Diverse gap junctions modulate distinct mechanisms for fiber cell formation during lens development and cataractogenesis
2006 StandoutNobel
Works of L. Olmos being referenced
Maladie de Cowden: a propos de 8 cas familiaux.
1979
Cocaine Dependence and Acute Cocaine Induce Decreases of Monocyte Proinflammatory Cytokine Expression across the Diurnal Period: Autonomic Mechanisms
2006
Embryonic and postnatal development of GABA, calbindin, calretinin, and parvalbumin in the mouse claustral complex
2004
Dynamic patterns of colocalization of calbindin, parvalbumin and GABA in subpopulations of mouse basolateral amygdalar cells during development
2007
Discrete element modeling of metallic powder sintering
2006
Double-Blind, Randomized Clinical Trial on the Effect of Interferon-Beta in the Treatment of Condylomata Acuminata
1994
Réticulo-histiocytome du dos de l’adulte
1974
Electric and magnetic properties of Fe–Ni powders–polymeric matrix composites
2006
Autosomal dominant zonular cataract with sutural opacities is associated with a splice mutation in the betaA3/A1-crystallin gene.
1998
A propos des basophiles dans l’infiltrat de l’eczéma experimental chez le cobaye
1976
[Cowden disease: report of 8 cases in 2 families (author's transl)].
1979