Christine Haag - Concepedia

Author

Christine Haag

Charité - Universitätsmedizin Berlin

Also Known As

C Haag, C Hååg, C. Haag, Christine Haag, Haag, Christine

Publications

741

Citations

H-Index

Concepts

All Affiliations

Charité - Universitätsmedizin Berlin European Molecular Biology Laboratory Friedrich-Alexander-Universität Erlangen-Nürnberg Universitätsklinikum Erlangen Heidelberg University

About

Christine Haag is an author at Charité - Universitätsmedizin Berlin specializing in medicine, chromosome 9, and quantitative genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	32
2	Public Health	1	1	21
3	Allergy	1	1	21
4	Allergy Medicine	1	1	21
5	Biology	1	1	11

Christine Haag

Publications

665

Citations

H-Index

Page 1

	Year	Citations
Prevalence and Clinical Spectrum of Nonsecretory Medullary Thyroid Carcinoma in a Series of 839 Patients with Sporadic Medullary Thyroid Carcinoma Karin Frank‐Raue, Andreas Machens, G. Leidig‐Bruckner, Thyroid	2012	114
Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German survey Friedhelm Raue, J. Pichl, Helmuth-G. Dörr, Clinical Endocrinology	2011	89
Novel Inactivating Mutations of the Calcium-Sensing Receptor: The Calcimimetic NPS R-568 Improves Signal Transduction of Mutant Receptors Ramona Rus, Christine Haag, Christiane Bumke‐Vogt, The Journal of Clinical Endocrinology & Metabolism	2008	74
Inactivating calcium‐sensing receptor mutations in patients with primary hyperparathyroidism Karin Frank‐Raue, G. Leidig‐Bruckner, Christine Haag, Clinical Endocrinology	2011	59
Novel Activating Mutations of the Calcium-Sensing Receptor: The Calcilytic NPS-2143 Mitigates Excessive Signal Transduction of Mutant Receptors Saskia Letz, Ramona Rus, Christine Haag, The Journal of Clinical Endocrinology & Metabolism	2010	58
The localisation of the extraneuronal monoamine transporter (EMT) in rat brain Christine Haag, Reinhard Berkels, Dirk Gründemann, Journal of Neurochemistry	2003	45
Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions Binsheng Gong, Dan Li, Rebecca Kusko, Genome biology	2021	38
CDC73-related hereditary hyperparathyroidism: five new mutations and the clinical spectrum Karin Frank‐Raue, Christine Haag, Egbert Schulze, European Journal of Endocrinology	2011	37
Heterozygous inactivating CaSR mutations causing neonatal hyperparathyroidism: function, inheritance and phenotype Markus Glaudo, Saskia Letz, Marcus Quinkler, European Journal of Endocrinology	2016	33
Amino Alcohol- (NPS-2143) and Quinazolinone-Derived Calcilytics (ATF936 and AXT914) Differentially Mitigate Excessive Signalling of Calcium-Sensing Receptor Mutants Causing Bartter Syndrome Type 5 and Autosomal Dominant Hypocalcemia Saskia Letz, Christine Haag, Egbert Schulze, PLoS ONE	2014	30

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