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Wolfanga L. Boson

Observed names: W Boson, W L Boson, W. Boson, W. L. Boson, W.L. Boson, W.L.M. Boson, Wolfanga Boson, Wolfanga Bóson, Wolfanga L Boson, Wolfanga L.M. Boson
OpenAlex ID: A5073729450
PTCH Gene Mutations in Odontogenic Keratocysts
2000 · D.C. Barreto, R.S. Gomez, et al. · Journal of Dental Research · 234
A Novel Mutation of the Cathepsin C Gene in Papillon‐Lefévre Syndrome
2002 · Vanessa F. Cury, José E. Costa, et al. · Journal of Periodontology · 58
Thiopurine methyltransferase polymorphisms in a Brazilian population
2003 · W L Boson, M A Romano-Silva, et al. · The Pharmacogenomics Journal · 45
Novel mutations of the BSCL2 and AGPAT2 genes in 10 families with Berardinelli–Seip congenital generalized lipodystrophy syndrome
2009 · Debora M. Miranda, Bernardo L. Wajchenberg, et al. · Clinical Endocrinology · 39
Familial suicide behaviour: association with probands suicide attempt characteristics and 5‐HTTLPR polymorphism
2004 · H. Correa, A. C. Campi‐Azevedo, et al. · Acta Psychiatrica Scandinavica · 35
Clonal composition of human adamantinomatous craniopharyngiomas and somatic mutation analyses of the patched (PTCH), Gsα and Gi2α genes
2001 · J.C. Sarubi, H. Bei, et al. · Neuroscience Letters · 35
Association of the serotonin transporter promoter polymorphism with suicidal behavior
2003 · A C Campi-Azevedo, W Boson, et al. · Molecular Psychiatry · 33
Sporadic cardiac myxomas and tumors from patients with Carney complex are not associated with activating mutations of the Gsα gene
1996 · Luiz DeMarco, Constantine A. Stratakis, et al. · Human Genetics · 32
Investigation of A218C tryptophan hydroxylase polymorphism: association with familial suicide behavior and proband's suicide attempt characteristics
2005 · M. M. Viana, L. A. De Marco, et al. · Genes Brain & Behavior · 31
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A homozygous cathepsin C mutation associated with Haim-Munk syndrome
2005 · V.F. Cury, R.S. Gomez, et al. · British Journal of Dermatology · 30
Nephrogenic diabetes insipidus: an X chromosome-linked dominant inheritance pattern with a vasopressin type 2 receptor gene that is structurally normal.
1994 · E Friedman, A E Bale, et al. · Proceedings of the National Academy of Sciences · 27
Molecular analysis of the WNT4 gene in 6 patients with Mayer-Rokitansky-Küster-Hauser syndrome
2007 · Juliana B. Drummond, Fernando M. Reis, et al. · Fertility and Sterility · 24
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Molecular analyses of the vasopressin type 2 receptor and aquaporin-2 genes in Brazilian kindreds with nephrogenic diabetes insipidus
1999 · Juliane L. Rocha, Eitan Friedman, et al. · Human Mutation · 20
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A signal peptide mutation of the arginine vasopressin gene in monozygotic twins
2003 · Wolfanga L. Boson, Juliana C. Sarubi, et al. · Clinical Endocrinology · 19
Analysis of T102C 5HT2A Polymorphism in Brazilian Psychiatric Inpatients: Relationship with Suicidal Behavior
2002 · H. Correa, L. De Marco, et al. · Cellular and Molecular Neurobiology · 19
Association study of T102C 5-HT2A polymorphism in schizophrenic patients: diagnosis, psychopathology, and suicidal behavior
2007 · Humberto Correa, Luiz De Marco, et al. · Dialogues in Clinical Neuroscience · 18
Odontogenic myxomas are not associated with activating mutations of the Gs alpha gene.
1998 · W L Boson, R S Gomez, et al. · PubMed · 16
Novel Vasopressin Type 2 ( AVPR2 ) Gene Mutations in Brazilian Nephrogenic Diabetes Insipidus Patients
2006 · W.L. Boson, T. Della Manna, et al. · Genetic Testing · 12
Nephrogenic Diabetes Insipidus (NDI): Clinical, Laboratory and Genetic Characterization of Five Brazilian Patients
2009 · Maria Helena Vaisbich, Juliana Carneiro, et al. · Clinics · 8
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Microsatellite Instability in Sporadic Parathyroid Adenoma1
2000 · Marta Sarquis, Eitan Friedman, et al. · The Journal of Clinical Endocrinology & Metabolism · 8
p.F508del in a heterogeneous cystic fibrosis population from Minas Gerais, Brazil
2008 · P.V.T. Vidigal, F.J.C. Reis, et al. · Brazilian Journal of Medical and Biological Research · 6
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Mutational Analyses of Candidate Genes in Human Squamous Cell Carcinomas
1999 · Andy Petroianu, Wolfanga L. Boson, et al. · The Laryngoscope · 5
Diabetes insipidus nefrogênico: conceitos atuais de fisiopatologia e aspectos clínicos
2000 · Juliane L. Rocha, Eitan Friedman, et al. · Arquivos Brasileiros de Endocrinologia & Metabologia · 3
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O papel do polimorfismo do gene p53 no desenvolvimento do cancer de colo uterino
2002 · Bruna Eugenia de Freitas, Juliana Moyses Barbosa Leite, et al. · RBM. Revista brasileira de medicina
Analise de mutações somáticas dos genes APP, presenilina 1 e 2, em tecido encefálico na doença de Alzheimer
1998 · Joao C Machado, Wolfanga L Boson, et al.
Works count: 25
Citation count: 757
H-index: 16
I10-index: 18
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