Wolfanga L. Boson - Concepedia

Author

Wolfanga L. Boson

Also Known As

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

Publications

760

Citations

H-Index

Concepts

All Affiliations

Universidade Federal de Minas Gerais Sheba Medical Center Hospital das Clínicas da Universidade Federal de Minas Gerais Universidade de São Paulo Dr. Euryclides Hospital de Jesus Zerbini

About

Wolfanga L. Boson is an author at Universidade Federal de Minas Gerais specializing in genetics, medicine, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	129
2	Social Sciences	1	1	18
3	Biology	1	1	19
4	Diabetes	1	1	19
5	Endocrinology	1	1	19

Wolfanga L. Boson

Publications

693

Citations

H-Index

Page 1

	Year	Citations
PTCH Gene Mutations in Odontogenic Keratocysts D.C. Barreto, Ricardo Santiago Gomez, A.E. Bale, Journal of Dental Research	2000	237
A Novel Mutation of the Cathepsin C Gene in Papillon‐Lefévre Syndrome Vanessa F. Cury, José E. Costa, Ricardo Santiago Gomez, Journal of Periodontology	2002	56
Thiopurine methyltransferase polymorphisms in a Brazilian population Wolfanga L. Boson, Marco Aurélio Romano‐Silva, Humberto Corrêa, The Pharmacogenomics Journal Brazilian PopulationGenetic DeterminantGeneticsHuman PolymorphismPopulation	2003	45
Novel mutations of the <i>BSCL2</i> and <i>AGPAT2</i> genes in 10 families with Berardinelli–Seip congenital generalized lipodystrophy syndrome Débora Marques de Miranda, B L Wajchenberg, Maria Regina Calsolari, Clinical Endocrinology	2009	37
Clonal composition of human adamantinomatous craniopharyngiomas and somatic mutation analyses of the patched (PTCH), Gsα and Gi2α genes Juliana Sarubi, H. Bei, Eric F. Adams, Neuroscience Letters GeneticsCraniofacial DevelopmentGi2α GenesSomatic Mutation AnalysesMolecular Genetics	2001	36
Familial suicide behaviour: association with probands suicide attempt characteristics and 5‐HTTLPR polymorphism Humberto Corrêa, Ana Carolina Campi‐Azevedo, Luiz De Marco, Acta Psychiatrica Scandinavica	2004	35
Sporadic cardiac myxomas and tumors from patients with Carney complex are not associated with activating mutations of the Gsα gene L DeMarco, Constantine A. Stratakis, Wolfanga L. Boson, Human Genetics Sporadic Cardiac MyxomasCardiac MuscleGeneticsCarney ComplexPathology	1996	32
Investigation of A218C tryptophan hydroxylase polymorphism: association with familial suicide behavior and proband's suicide attempt characteristics Melissa Machado Viana, Luiz Marco, Wolfanga L. Boson, Genes Brain & Behavior	2005	31
A homozygous cathepsin C mutation associated with Haim-Munk syndrome Vanessa F. Cury, Ricardo Santiago Gomez, J. E. Costa, British Journal of Dermatology	2005	29
Nephrogenic diabetes insipidus: an X chromosome-linked dominant inheritance pattern with a vasopressin type 2 receptor gene that is structurally normal. Eitan Friedman, A. Bale, Emma Carson, Proceedings of the National Academy of Sciences	1994	27

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