Déborah Morris-Rosendahl

Author

Also Known As

D J Morris-Rosendahl, D Morris-Rosendahl, D. J. Morris-Rosendahl, D. Morris-Rosendahl, D.J. Morris-Rosendahl, D.J. Morris‐Rosendahl, D.J. Morris–Rosendahl, Deborah J Morris-Rosendahl, Deborah J. Morris-Rosendahl, Deborah J. Morris‐Rosendahl

153

Publications

Citations

H-Index

Concepts

All Affiliations

University of Freiburg Imperial College London Royal Brompton & Harefield NHS Foundation Trust Centre hospitalier de Rouffach University Medical Center Freiburg

About

Déborah Morris-Rosendahl is an author at University of Freiburg specializing in medicine, genetics, and biological psychiatry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	23	1.5K
2	Public Health	3	3	131
3	Social Sciences	3	3	177
4	Health Sciences	1	1	103
5	Cell Biology	1	1	42

Déborah Morris-Rosendahl

Publications

2.9K

Citations

H-Index

Page 1

	Year	Citations
The core <i>FOXG1</i> syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis Fanny Kortüm, Soma Das, M. Flindt, Journal of Medical Genetics	2011	246
Isolation of a novel potassium channel gene hSKCa3 containing a polymorphic CAG repeat: a candidate for schizophrenia and bipolar disorder? K. George Chandy, Emmanuelle Fantino, Oliver H. Wittekindt, Molecular Psychiatry Molecular NeuroscienceSignal TransductionHyperpolarization (Biology)GeneticsPsychiatric Genetics	1998	208
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry Julia Wallmeier, Diana Frank, Amelia Shoemark, The American Journal of Human Genetics Developmental BiologyGenetic DisorderGeneticsPathologyMotile Ciliopathy	2019	201
Loss-of-Function Mutations in TBC1D20 Cause Cataracts and Male Infertility in blind sterile Mice and Warburg Micro Syndrome in Humans Ryan P. Liegel, Mark T. Handley, Adam Ronchetti, The American Journal of Human Genetics Genetic DisorderGeneticsPathogenesisPathologyMolecular Genetics	2013	132
Brief research communication: serotonin transporter (5-HTT) gene polymorphisms are not associated with susceptibility to mood disorders Margret R. Hoehe, Birgit Wendel, Ingrid Grunewald, American Journal of Medical Genetics Psychiatric DisordersGeneticsGenetic EpidemiologyHuman PolymorphismPsychology	1998	123
Mutations in STAMBP, encoding a deubiquitinating enzyme, cause microcephaly–capillary malformation syndrome Laura M. McDonell, Ghayda Mirzaa, Diana Alcantara, Nature Genetics Developmental BiologyPathogenesisVascular MalformationPathologyDeubiquitinating Enzyme	2013	116
Topological data analysis reveals genotype–phenotype relationships in primary ciliary dyskinesia Amelia Shoemark, Bruna Rubbo, Marie Legendre, European Respiratory Journal	2021	104
Disturbed Wnt Signalling due to a Mutation in CCDC88C Causes an Autosomal Recessive Non-Syndromic Hydrocephalus with Medial Diverticulum Arif B. Ekici, D. Hilfinger, M. Jatzwauk, Molecular Syndromology Medial DiverticulumBrain DevelopmentGeneticsDisease Gene IdentificationSynaptic Signaling	2010	103
CardioClassifier: disease- and gene-specific computational decision support for clinical genome interpretation Nicola Whiffin, Roddy Walsh, Risha Govind, Genetics in Medicine	2018	101
Clinical utility of NGS diagnosis and disease stratification in a multiethnic primary ciliary dyskinesia cohort Mahmoud R. Fassad, Mitali Patel, Amelia Shoemark, Journal of Medical Genetics	2019	91

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