Jürgen Herrmann - Concepedia

Author

Jürgen Herrmann

Shodair Children's Hospital

Also Known As

Jurgen Herrmann, Jurgen P. Herrmann, Jurgen P.R. Herrmann, Jürgen Herrmann, Jürgen P. R. Herrmann

Publications

1.4K

Citations

H-Index

Concepts

All Affiliations

Shodair Children's Hospital University of Wisconsin–Madison Oklahoma State University Center for Health Sciences Houston Methodist

About

Jürgen Herrmann is an author at Shodair Children's Hospital specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	449
2	Natural Sciences	2	2	176
3	Biology	2	2	176
4	Public Health	1	1	84
5	Gender Studies	1	1	84

Jürgen Herrmann

Publications

Citations

H-Index

Page 1

	Year	Citations
New multiple congenital anomalies/mental retardation syndrome with cardio‐facio‐cutaneous involvement—the CFC syndrome James F. Reynolds, Giovanni Neri, Jürgen Herrmann, American Journal of Medical Genetics	1986	219
MALDI-TOF mass spectrometry – a rapid method for the identification of dermatophyte species Pietro Nenoff, Marcel Erhard, Jan C. Simon, Medical Mycology Maldi-tof Mass SpectrometryBiological Mass SpectrometryDermatophyte SpeciesRapid MethodDermatology	2012	144
Some considerations bearing on the doctrine of self‐fulfilling prophecy in sex chromosome aneuploidy Mary Puck, Jürgen Herrmann American Journal of Medical Genetics FertilityCytogeneticsSelf-fulfilling ProphecyGeneticsGynecology	1981	84
Significance of phenotypic and chromosomal abnormalities in X‐linked mental retardation (Martin‐Bell or Renpenning syndrome) Mark T. Jennings, Judith G. Hall, Holger Hoehn, American Journal of Medical Genetics	1980	79
AUTOSOMAL-DOMINANT SEX-DEPENDENT TRANSMISSION OF THE WIEDEMANN-BECKWITH SYNDROME Mark Lubinsky, Jürgen Herrmann, AndrewL. Kosseff, The Lancet Mendelian DisorderGenetic DisorderThe Wiedemann-beckwith SyndromeGeneticsAbnormal Development	1974	66
Further delineation of the C (trigonocephaly) syndrome Ray M. Antley, Do Sung Hwang, W Theopold, American Journal of Medical Genetics	1981	60
Studies of malformation syndromes of man XXIX: The Wiedemann-Beckwith syndrome Andrew L. Kosseff, Jürgen Herrmann, Enid F. Gilbert, European Journal of Pediatrics Developmental AnomalyMendelian DisorderMalformation SyndromesCongenital DisordersPathology	1976	56
THE WIEDEMANN-BECKWITH SYNDROME: GENETIC CONSIDERATIONS AND A DIAGNOSTIC SIGN AndrewL. Kosseff, Jürgen Herrmann, JohnM. Opitz The Lancet Developmental AnomalyMendelian DisorderGenetic DisorderNeuropathologyMedicine	1972	42
Short rib‐polydactyly syndrome, type 3 with chondrocytic inclusions: Report of a case and review of the literature S. Samuel Yang, Ching‐Shen Lin, A. Al Saadi, American Journal of Medical Genetics Developmental AnomalyType 1Chondrocytic InclusionsDevelopmental BiologySurgical Pathology	1980	41
Studies of malformation syndromes of humans XXXIIIC: The FG syndrome — further studies on three affected individuals from the FG family John M. Opitz, Elizabeth G. Kaveggia, William N. Adkins, American Journal of Medical Genetics	1982	35

Page 1