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C. Woellner · SciRah

Researcher profile · Semantic Scholar

C. Woellner

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C. Woellner — researcher profile on SciRah

h-index: 18
Works: 69
Citations: 5,473

Most-cited papers

Inflammatory Bowel Disease and Mutations Affecting the Interleukin-10 Receptor
E. Glocker, D. Kotlarz, K. Boztug, E. Gertz +24 more
2009New England Journal of Medicine1,394 citations Open access
Semantic Scholar
STAT3 mutations in the hyper-IgE syndrome.
S. Holland, F. DeLeo, H. Elloumi, Amy P. Hsu +21 more
2007New England Journal of Medicine1,189 citations Open access
Semantic Scholar
A Homozygous CARD9 Mutation in a Family with Susceptibility to Fungal Infections
E. Glocker, A. Hennigs, M. Nabavi, A. Schäffer +15 more
2009New England Journal of Medicine792 citations Open access
Semantic Scholar
An antibody-deficiency syndrome due to mutations in the CD19 gene.
M. V. van Zelm, I. Reisli, M. van der Burg, Diana Castaño +7 more
2006New England Journal of Medicine538 citations Open access
Semantic Scholar
Large Deletions and Point Mutations Involving DOCK8 in the Autosomal Recessive Form of the Hyper-IgE Syndrome
K. Engelhardt, S. Mcghee, S. Winkler, A. Sassi +34 more
2009Journal of Allergy and Clinical Immunology509 citations Open access
Semantic Scholar
Mutations in the signal transducer and activator of transcription 3 (STAT3) and diagnostic guidelines for the Hyper-IgE Syndrome
C. Woellner, E. Gertz, A. Schäffer, M. Lagos +43 more
2010Journal of Allergy and Clinical Immunology282 citations Open access
Semantic Scholar
Chédiak-Higashi syndrome
Nils Peters, Martin Dichgans, S. Surendran, Josep M. Argilés +174 more
2020Definitions128 citations Open access
Semantic Scholar
Congenital sucrase-isomaltase deficiency
Nils Peters, Martin Dichgans, S. Surendran, Josep M. Argilés +174 more
2020Definitions77 citations Open access
Semantic Scholar
Reduced memory B cells in patients with hyper IgE syndrome.
C. Speckmann, A. Enders, C. Woellner, D. Thiel +14 more
2008Clinical Immunology77 citations
Semantic Scholar
The hyper IgE syndrome and mutations in TYK2.
C. Woellner, A. Schäffer, J. Puck, E. Renner +4 more
2007Immunity63 citations Open access
Semantic Scholar
Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome (vol 124, pg 1289, 2009)
K. Engelhardt, S. Mcghee, S. Winkler, A. Sassi +34 more
201060 citations
Semantic Scholar
Congenital dysfibrinogenemia.
Nils Peters, Martin Dichgans, S. Surendran, Josep M. Argilés +174 more
1984Current problems in clinical biochemistry49 citations
Semantic Scholar
CHLAMYDIA INFECTION
N. Peters, M. Dichgans, S. Surendran, Josep M. Argilés +174 more
201845 citations
Semantic Scholar
Screening of functional and positional candidate genes in families with common variable immunodeficiency
U. Salzer, C. Neumann, J. Thiel, C. Woellner +13 more
2008BMC Immunology42 citations Open access
Semantic Scholar
An immune defect causing dominant chronic mucocutaneous candidiasis and thyroid disease maps to chromosome 2p in a single family.
T. Atkinson, A. Schäffer, B. Grimbacher, H. Schroeder +3 more
2001American Journal of Human Genetics40 citations Open access
Semantic Scholar
Crigler-Najjar syndrome
Nils Peters, Martin Dichgans, S. Surendran, Josep M. Argilés +174 more
2020Definitions21 citations Open access
Semantic Scholar
Chronic Idiopathic Intestinal Pseudo-obstruction
N. Peters, M. Dichgans, S. Surendran, Josep M. Argilés +174 more
201119 citations
Semantic Scholar
Plasticity of secondary structure in the N-terminal region of β-dystroglycan
A. Boffi, M. Bozzi, F. Sciandra, C. Woellner +3 more
200119 citations
Semantic Scholar
Pneumocystis jirovecii pneumonia in a baby with hyper-IgE syndrome
B. Garty, A. Ben-Baruch, A. Rolinsky, C. Woellner +2 more
2009European Journal of Pediatrics14 citations
Semantic Scholar
Reduced Bone Density in Patients with Autosomal Dominant Hyper-IgE Syndrome
O. Scheuerman, V. Hoffer, A. Cohen, C. Woellner +2 more
2013Journal of Clinical Immunology13 citations
Semantic Scholar
Toll-Like Receptor Stimulation Induces Higher TNF-α Secretion in Peripheral Blood Mononuclear Cells from Patients with Hyper IgE Syndrome
M. Yeganeh, P. Henneke, N. Rezaei, S. Ehl +15 more
2008International Archives of Allergy and Immunology12 citations Open access
Semantic Scholar
Hypertrophic pulmonary osteoarthropathy
D. Metze, V. F. Cury, R. Gomez, L. Marco +193 more
200911 citations
Semantic Scholar
Chylomicron retention disease
Nils Peters, M. Dichgans, S. Surendran, Josep M. Argilés +174 more
2020Definitions9 citations Open access
Semantic Scholar
Challenges of genetic counseling in patients with autosomal dominant diseases, such as the hyper-IgE syndrome (STAT3-HIES).
B. Spielberger, C. Woellner, G. Dueckers, J. Sawalle-Belohradsky +8 more
2012Journal of Allergy and Clinical Immunology9 citations Open access
Semantic Scholar
Community acquired Staphylococcus aureus meningitis and cerebral abscesses in a patient with a hyper-IgE and a Dubowitz-like syndrome.
M. Beitzke, C. Enzinger, C. Windpassinger, D. Pfeifer +4 more
2011Journal of Neurological Sciences8 citations
Semantic Scholar
Hypoxanthine-guanine phosphoribosyltransferase deficiency
D. Metze, V. F. Cury, R. Gomez, L. Marco +193 more
2020Definitions6 citations Open access
Semantic Scholar
The hyper-IgE syndrome is not caused by a microdeletion syndrome
D. Pfeifer, C. Woellner, Astrid Petersen, M. Pietrogrande +8 more
2007Immunogenetics6 citations
Semantic Scholar
Human transmissible spongiform encephalopathies
D. Metze, V. F. Cury, R. Gomez, L. Marco +193 more
20026 citations
Semantic Scholar
Hypersensitivity vasculitis.
D. Metze, V. F. Cury, R. Gomez, L. Marco +193 more
1978Journal of the Indian Medical Association6 citations
Semantic Scholar
Novel humoral immunodeficiency in humans associated with deleterious homozygous mutation in CD19.
Diana Castaño, P. Patiño, C. Woellner, U. Salzer +5 more
20055 citations
Semantic Scholar
Plasticity of secondary structure in the N-terminal region of beta-dystroglycan.
A. Boffi, M. Bozzi, F. Sciandra, C. Woellner +3 more
2001Biochimica et Biophysica Acta5 citations
Semantic Scholar
Chronic mucocutaneous candidiasis is associated with a homozygous mutation in CARD9
B. Grimbacher, A. Hennigs, M. Nabavi, E. Glocker +8 more
20083 citations
Semantic Scholar
Hereditary hyperekplexia
D. Metze, V. F. Cury, R. Gomez, L. Marco +193 more
2020Definitions2 citations Open access
Semantic Scholar
Susceptibility to fungal infections due to a homozygous mutation in CARD9
E. Glocker, A. Hennigs, M. Nabavi, A. Schäffer +15 more
20102 citations
Semantic Scholar
Early-onset inflammatory bowel disease caused by mutant IL10 receptor
E. Glocker, D. Kotlarz, K. Boztug, E. Gertz +24 more
2010Journal of Translational Medicine2 citations Open access
Semantic Scholar
Genetic and functional characterisation of the autosomal dominant form of Hyper IgE Syndrome
C. Woellner
20141 citations
Semantic Scholar
DOCK8 Deletions and Mutations Are Associated With The Autosomal Recessive Hyper-IgE Phenotype
S. Mcghee, K. Engelhardt, S. Winkler, A. Sassi +21 more
20101 citations Open access
Semantic Scholar
Severe Early-Onset Inflammatory Bowel Disease Caused by IL10 Receptor Deficiency Can Be Cured by Allogeneic Hematopoietic Stem Cell Transplantation.
K. Boztug, D. Kotlarz, E. Glocker, M. Gertz +24 more
20091 citations
Semantic Scholar
[Caroli's syndrome].
Nils Peters, Martin Dichgans, S. Surendran, Josep M. Argilés +174 more
2019RöFo. Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren (Print)0 citations
Semantic Scholar
CHOROIDEREMIA
Nils Peters, Martin Dichgans, S. Surendran, Josep M. Argilés +174 more
2019Retina0 citations
Semantic Scholar
Cryptogenic Fibrosing Alveolitis
Nils Peters, Martin Dichgans, S. Surendran, Josep M. Argilés +174 more
20150 citations
Semantic Scholar
Reduced Bone Density in Patients with Autosomal Dominant Hyper-IgE Syndrome
O. Scheuerman, V. Hoffer, A. Cohen, C. Woellner +2 more
2013Journal of Clinical Immunology0 citations
Semantic Scholar
Congestive hepatopathy
Nils Peters, Martin Dichgans, S. Surendran, Josep M. Argilés +174 more
2013Radiopaedia.org0 citations
Semantic Scholar
Chronic Bullous Disease of Childhood
Nils Peters, Martin Dichgans, S. Surendran, Josep M. Argilés +174 more
20110 citations
Semantic Scholar
Immune deficiencies , infection , and systemic immune disorders Mutations in STAT 3 and diagnostic guidelines for hyper-IgE syndrome
C. Woellner, E. Gertz, A. Schäffer, M. Lagos +40 more
20100 citations
Semantic Scholar
Severe early onset ileo-colitis can be caused by mutations in IL10RB and successfully treated by allogeneic hematopoietic stem cell transplantation
E. Glocker, A. Schäffer, M. Perro, A. Allroth +10 more
20100 citations
Semantic Scholar
Thirty-eight of 47 patients with autosomal-recessive hyper-IgE syndrome carry deletions and point mutations in Dock8
K. Engelhardt, S. Mcghee, S. Winkler, L. Graham +51 more
20100 citations
Semantic Scholar
高IgE症候群(HIGE)患者における免疫固相化アレルゲンチップ(ISAC)を用いた血清IgEレパートリーの解析
A. Heaps, T. El-shanawany, C. Selwood, M. Moody +6 more
20100 citations
Semantic Scholar
Cornea Farinata and other Variants
W. Lisch, A. Janecke, B. Seitz, J. Wierzba +174 more
20090 citations
Semantic Scholar
WSC 05 ‐ Deficiencies of the Innate Immune System
Lytic, Function, S. Torres, G. Zaldivar +37 more
20090 citations Open access
Semantic Scholar

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