Astrid Golla - Concepedia

Concepedia

Author

Astrid Golla

Ludwig-Maximilians-Universität München

Also Known As

A Golla, A. Golla, Astrid Golla

32

Publications

1.1K

Citations

16

H-Index

40

Concepts

All Affiliations

Ludwig-Maximilians-Universität München University of Bonn Universitätskinderklinik Technical University of Munich Salzburger Landeskliniken

AG

About

Astrid Golla is an author at Ludwig-Maximilians-Universität München specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	596
2	Biology	2	2	109
3	Natural Sciences	1	1	86
4	Cell Biology	1	1	42
5	Molecular Biology	1	1	86

Astrid Golla

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17

Publications

1.1K

Citations

16

H-Index

	Year	Citations
Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22 Astrid Golla, Annette Jansson, Juliane Ramser, European Journal of Human Genetics GeneticsPathologySusceptibility GeneMolecular GeneticsMedicine	2002	185
Heritability of Carotid Artery Atherosclerotic Lesions Susanna Moskau, Astrid Golla, Christoph Grothe, Stroke	2004	110
Limited relevance of the <i>CHEK2</i> gene in hereditary breast cancer Michael R. Dufault, Beate Betz, Barbara Wappenschmidt, International Journal of Cancer	2004	92
Genotype–phenotype analysis in Apert syndrome suggests opposite effects of the two recurrent mutations on syndactyly and outcome of craniofacial surgery Steven von Gernet, Astrid Golla, Y Ehrenfels, Clinical Genetics GeneticsGenetic EpidemiologyPathologyMaxillofacial GrowthSurgery	2000	86
Familial Mental Retardation Syndrome ATR-16 Due to an Inherited Cryptic Subtelomeric Translocation, t(3;16)(q29;p13.3) Elke Holinski‐Feder, Edwin Reyniers, Sabine Uhrig, The American Journal of Human Genetics Down SyndromeMendelian DisorderPsychiatryGenetic DisorderGenetics	2000	86
Wiskott-Aldrich syndrome: no strict genotype-phenotype correlations but clustering of missense mutations in the amino-terminal part of the WASP gene product Dirk Schindelhauer, Michael Weiss, Heide Hellebrand, Human Genetics BiologyAllelic VariantStrict Genotype-phenotype CorrelationsMendelian DisorderGenetic Disorder	1996	86
Evidence for genetic heterogeneity of malignant hyperthermia susceptibility. Thomas Deufel, Astrid Golla, David Iles, PubMed	1992	77
Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26 Axel M. Hillmer, Antònia Flaquer, S. Hanneken, The American Journal of Human Genetics Genetic DisorderGeneticsLinkage AnalysisChromosome BiologyMolecular Genetics	2008	76
Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232. Thomas Meitinger, Babett Heye, Christine Petit, PubMed	1990	69
Exclusion of malignant hyperthermia susceptibility (MHS) from a putative MHS2 locus on chromosome 17q and of the α1, β1, and γ subunits of the dihydropyridine receptor calcium channel as candidates for the molecular defect Ralf Sudbrak, Astrid Golla, Kirk J. Hogan, Human Molecular Genetics	1993	43

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