Klaus Schmitz‐Abe - Concepedia

Author

Klaus Schmitz‐Abe

Also Known As

German Retinal Vein Occlusion Group, K Schmitz, K. E. F. Schmitz, K. SCHMITZ, K. Schmitz, K. Schmitz-Abe, KLAUS Schmitz, Kai Schmitz, Klaus E. Schmitz, Klaus Erich Schmitz Abe

174

Publications

4.3K

Citations

H-Index

141

Concepts

All Affiliations

Boston Children's Hospital Harvard University Dana-Farber/Boston Children's Cancer and Blood Disorders Center Broad Institute University of Cologne

About

Klaus Schmitz‐Abe is an author at Boston Children's Hospital specializing in medicine, biology, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	19	1.1K
2	Natural Sciences	8	8	305
3	Engineering	6	6	226
4	Health Sciences	4	4	178
5	Public Health	1	1	24

Klaus Schmitz‐Abe

Publications

3.2K

Citations

H-Index

Page 1

	Year	Citations
Using Whole-Exome Sequencing to Identify Inherited Causes of Autism Timothy W. Yu, Maria H. Chahrour, Michael E. Coulter, Neuron Whole-exome SequencingGeneticsSyndromic AutismAutism	2013	456
Recessive truncating titin gene, <i>TTN</i> , mutations presenting as centronuclear myopathy Ozge Ceyhan‐Birsoy, Pankaj B. Agrawal, Carlos Hidalgo, Neurology	2013	213
Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD) Pranesh Chakraborty, Klaus Schmitz‐Abe, Erin K. Kennedy, Blood	2014	176
Notch4 signaling limits regulatory T-cell-mediated tissue repair and promotes severe lung inflammation in viral infections Hani Harb, Mehdi Benamar, Peggy S. Lai, Immunity InflammationInflammatory Lung DiseaseLung InflammationT-regulatory CellImmunology	2021	119
Ductal epithelial proliferations of the breast: a biological continuum? Comparative genomic hybridization and high‐molecular‐weight cytokeratin expression patterns Werner Boecker, Horst Buerger, Klaus Schmitz‐Abe, The Journal of Pathology	2001	111
Dominant-negative mutations in human <i>IL6ST</i> underlie hyper-IgE syndrome Vivien Béziat, Simon J. Tavernier, Yin‐Huai Chen, The Journal of Experimental Medicine ImmunodeficienciesImmunologyPathologyImmunotherapyStat3 Mutations	2020	109
A regulatory T cell Notch4–GDF15 axis licenses tissue inflammation in asthma Hani Harb, Emmanuel Stephen‐Victor, Elena Crestani, Nature Immunology InflammationAsthmaImmune Cell DevelopmentT-regulatory CellImmune Regulation	2020	109
ClinPhen extracts and prioritizes patient phenotypes directly from medical records to expedite genetic disease diagnosis Cole A. Deisseroth, Johannes Birgmeier, Ethan E. Bodle, Genetics in Medicine Genetic DiseasesMedical RecordsMedicineGeneticsGenetic Disease Diagnosis	2018	107
Neuromuscular Evaluation of Trunk-Training Exercises. Peter Konrad, Klaus Schmitz‐Abe, Achim Denner PubMed Muscle FunctionNeuromuscular CoordinationHealthy SubjectsMotor ControlRaw Emg Signals	2001	97
Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination Tojo Nakayama, Almundher Al‐Maawali, Malak El‐Quessny, The American Journal of Human Genetics	2015	79

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