H. Collmann - Concepedia

Author

H. Collmann

University of Würzburg

Also Known As

Collmann H., H Collmann, H. Collmann, Hartmut Collmann

101

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

University of Würzburg Universitätsklinikum Würzburg Klinikum Oldenburg Freie Universität Berlin National Human Genome Research Institute

About

H. Collmann is an author at University of Würzburg specializing in medicine, orthopaedics, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	24	927
2	Anatomy	6	6	247
3	Health Sciences	3	3	141
4	Social Sciences	1	1	10
5	Cognitive Science	1	1	10

H. Collmann

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Saethre–Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome Christian Schropp, Gabriele Lieb, Birgit Petersen, European Journal of Human Genetics Twist 1Developmental BiologyGenetic DisorderGeneticsSaethre–chotzen Syndrome	2005	146
Surgical management of tethered spinal cord in adults: report of 54 cases Sabine Hüttmann, Jüergen Krauss, H. Collmann, Journal of Neurosurgery Spine	2001	120
Neurosurgical aspects of childhood hypophosphatasia H. Collmann, Étienne Mornet, Stefan Gattenlöhner, Child s Nervous System Pediatric Brain TumorsPediatric HydrocephalusPediatric NeurosurgeryNeuroanatomyPediatrics	2008	97
Avoiding CT scans in children with single-suture craniosynostosis T. Schweitzer, H. Böhm, Philipp Meyer‐Marcotty, Child s Nervous System Medical ImagingPediatricsCraniofacial AnomaliesCt ScansCraniofacial Surgery	2012	87
Cutaneous lesions in occult spinal dysraphism—correlation with intraspinal findings Christian Schropp, N. Sörensen, H. Collmann Child s Nervous System Surgical PathologySpinal TumorDermatologyNeuropathologyMedicine	2005	79
Mutations in the interleukin receptor <i><scp>IL</scp>11<scp>RA</scp></i> cause autosomal recessive Crouzon‐like craniosynostosis Katharina Keupp, Yun Li, İbrahim Vargel, Molecular Genetics & Genomic Medicine	2013	75
Effective NSAID treatment indicates that hyperprostaglandinism is affecting the clinical severity of childhood hypophosphatasia HJ Girschick, P. Schneider, Imme Haubitz, Orphanet Journal of Rare Diseases	2006	66
Hydrocephalus in craniosynostosis H. Collmann, N. Sörensen, J. Mühling Child s Nervous System Pediatric HydrocephalusCerebrospinal FluidCraniofacial AnomaliesNeurologyAnatomy	1988	57
An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly Birgit Petersen, H. Collmann, T. Grimm Cytogenetic and Genome Research Developmental AnomalyThumb HypoplasiaDevelopmental BiologyMendelian DisorderOphthalmology	2000	57
Clustering of FGFR2 gene mutations inpatients with Pfeiffer and Crouzon syndromes (FGFR2-associated craniosynostoses) H. Collmann, Madleen Busse, B. Halliger–Keller, Cytogenetic and Genome Research Mendelian DisorderGenetic DisorderGeneticsFgfr MutationsGenetic Epidemiology	2000	49

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