Gerhard Neuhäuser - Concepedia

Author

Gerhard Neuhäuser

Oklahoma State University Center for Health Sciences

Also Known As

G NEUHAEUSER, G Neuhäuser, G. NEUHÄUSER, G. Neuhauser, G. Neuhäuser, Gerhard Neuhauser, Gerhard Neuhäuser, Neuhäuser, Gerhard

240

Publications

871

Citations

H-Index

Concepts

All Affiliations

Oklahoma State University Center for Health Sciences University of Wisconsin–Madison Wisconsin Disability Association Friedrich-Alexander-Universität Erlangen-Nürnberg Justus-Liebig-Universität Gießen

About

Gerhard Neuhäuser is an author at Oklahoma State University Center for Health Sciences specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	135
2	Education	1	1	23
3	Health Sciences	1	1	19
4	Anatomy	1	1	77
5	Immunology	1	1	19

Gerhard Neuhäuser

Publications

340

Citations

H-Index

Page 1

	Year	Citations
Autosomal recessive syndrome of cerebellar ataxia and hypogonadotropic hypogonadism* Gerhard Neuhäuser, John M. Opitz Clinical Genetics	1975	89
“ADAM complex” (amniotic deformity, adhesions, mutilations)—A pattern of craniofacial and limb defects H. Keller, Gerhard Neuhäuser, M. Virginia Durkin‐Stamm, American Journal of Medical Genetics GeneticsAdam ComplexAnatomyOrthopaedic SurgeryEmbryology	1978	77
Autosomal recessive syndrome of pseudogliomatous blindness, osteoporosis and mild mental retardation Gerhard Neuhäuser, Elisabeth G. Kaveggia, John M. Opitz Clinical Genetics	1976	40
[Internalizing and externalizing syndrome in reading and writing disorders]. Andreas Bäcker, Gerhard Neuhäuser PubMed Language DevelopmentEducationPsycholinguisticsMental HealthReading Disabilities	2003	23
CNS late effects after ALL therapy in childhood. Part II: Conventional EEG recordings in asymptomatic long-term survivors of childhood ALL- An evaluation of the interferences between neurophysiology, neurology, psychology, and CNS morphology Michael A. Ueberall, D. Wénzel, Holger Hertzberg, Medical and Pediatric Oncology	1997	22
Heterogeneity of X‐linked recessive (Spino)cerebellar ataxia with or without spastic diplegia Selçuk Apak, Memnune Yüksel, Meral Özmen, American Journal of Medical Genetics	1989	21
CYTOPLASMIC INCLUSIONS IN A CHILD AFFECTED WITH KRABBEʼS DISEASE (GLOBOID LEUCODYSTROPHY) AND IN THE RABBIT INJECTED WITH GALACTOCEREBROSIDES A. P. Anzil, K. Blinzinger, P. MEHRAELN, Journal of Neuropathology & Experimental Neurology ImmunohematologyGermany SearchAutoimmune DiseaseG. DornImmunodeficiencies	1972	19
Familial spastic paraplegia with distal muscle wasting in the Old Order Amish; atypical Troyer syndrome or “new” syndrome* Gerhard Neuhäuser, Colette Wiffler, John M. Opitz Clinical Genetics	1976	19
Benign Hereditary Non-Progressive Chorea of Early Onset<sup>1</sup>– Clinical Genetics of the syndrome and report of a New Family Joshua Burns, Gerhard Neuhäuser, Lawrence G. Tomasi Neuropediatrics New FamilyParamyoclonus MultiplexDominant GeneMendelian DisorderGenetic Disorder	1976	16
X‐linked congenital ataxia: A new locus maps to Xq25‐q27.1 Ginevra Zanni, Enrico Bertini, Cecelia Bellcross, American Journal of Medical Genetics Part A	2008	14

Page 1