Sigrun Wohlfart - Concepedia

Author

Sigrun Wohlfart

Universitätsklinikum Erlangen ORCID

Also Known As

S Wohlfart, S. Wohlfart, Sigrun Maier-Wohlfart, Sigrun Wohlfart

Publications

651

Citations

H-Index

Concepts

All Affiliations

Universitätsklinikum Erlangen Friedrich-Alexander-Universität Erlangen-Nürnberg Edimer Pharmaceuticals (United States)Université Paris Cité Cardiff University

About

Sigrun Wohlfart is an author at Universitätsklinikum Erlangen specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	302
2	Endocrinology	1	1	170
3	Molecular Genetics	1	1	39
4	Obstetrics	1	1	170
5	Pathology	1	1	39

Sigrun Wohlfart

Publications

610

Citations

H-Index

Page 1

	Year	Citations
Prenatal Correction of X-Linked Hypohidrotic Ectodermal Dysplasia Holm Schneider, Florian Faschingbauer, Sonia Schuepbach‐Mallepell, New England Journal of Medicine GeneticsReproductive HealthGynecologyEmbryologyAbnormal Development	2018	170
Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity Rami Abou Jamra, Sigrun Wohlfart, Markus Zweier, European Journal of Human Genetics Genetic DisorderMedicineGeneticsGenetic EpidemiologyLinkage Analysis	2011	93
Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly Update Nicolai Peschel, J. Timothy Wright, Maranke I. Koster, Genes	2022	49
Automatic recognition of the <scp>XLHED</scp> phenotype from facial images S. Hadj‐Rabia, Holm Schneider, Elena Navarro, American Journal of Medical Genetics Part A	2017	48
Genotype–phenotype correlation in boys with X‐linked hypohidrotic ectodermal dysplasia Kristin Burger, Anne‐Theres Schneider, Sigrun Wohlfart, American Journal of Medical Genetics Part A	2014	45
Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study Sigrun Wohlfart, Ralph Meiller, Johanna Hammersen, Orphanet Journal of Rare Diseases	2020	42
Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements Sigrun Wohlfart, Johanna Hammersen, Holm Schneider Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsBreakpoint MappingPathology	2016	39
A novel missense mutation in the gene <i>EDARADD</i> associated with an unusual phenotype of hypohidrotic ectodermal dysplasia Sigrun Wohlfart, Stephan Söder, Asma Smahi, American Journal of Medical Genetics Part A	2015	35
Reliability of prenatal detection of X‐linked hypohidrotic ectodermal dysplasia by tooth germ sonography Johanna Hammersen, Sigrun Wohlfart, Tamme W. Goecke, Prenatal Diagnosis	2018	27
Maternal SARS-CoV-2 infection during pregnancy: possible impact on the infant Patrick Morhart, Christian Y. Mardin, Manfred Rauh, European Journal of Pediatrics	2021	25

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