Erich Roessler - Concepedia

Author

Erich Roessler

National Institutes of Health

Also Known As

Blake Carrington, Daniel Pineda-Alvarez, E Roessler, E. Roessler, ERICH ROESSLER, Erich Roessler, Thomas Winder

112

Publications

10.4K

Citations

H-Index

103

Concepts

All Affiliations

National Institutes of Health National Human Genome Research Institute Children's Hospital of Philadelphia University of Pennsylvania Baylor College of Medicine

About

Erich Roessler is an author at National Institutes of Health specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	35	45	7.1K
2	Public Health	3	3	120
3	Natural Sciences	2	2	66
4	Engineering	1	1	19
5	Health Sciences	1	1	38

Erich Roessler

Publications

9.1K

Citations

H-Index

Page 1

	Year	Citations
Mutations in the human Sonic Hedgehog gene cause holoprosencephaly Erich Roessler, Elena Belloni, Karin Gaudenz, Nature Genetics Knockout MouseDevelopmental BiologyGenetic DisorderGeneticsMorphogenesis	1996	1.2K
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly Elena Belloni, Maximilian Muenke, Erich Roessler, Nature Genetics Knockout MouseDevelopmental BiologyGeneticsMorphogenesisMedicine	1996	644
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly Deeann Wallis, Erich Roessler, Ute Hehr, Nature Genetics Developmental BiologyGenetic DisorderGeneticsAutophagyMolecular Genetics	1999	427
The interleukin (IL) 2 receptor beta chain is shared by IL-2 and a cytokine, provisionally designated IL-T, that stimulates T-cell proliferation and the induction of lymphokine-activated killer cells. Richard N. Bamford, Angus Grant, J. D. Burton, Proceedings of the National Academy of Sciences T-regulatory CellImmune RegulationImmunologyImmunodominanceImmunologic Mechanism	1994	412
A lymphokine, provisionally designated interleukin T and produced by a human adult T-cell leukemia line, stimulates T-cell proliferation and the induction of lymphokine-activated killer cells. J. D. Burton, Richard N. Bamford, Christian Peters, Proceedings of the National Academy of Sciences T-regulatory CellImmunologyImmune RegulationImmunologic MechanismInterleukin T	1994	397
Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination Karen W. Gripp, David Wotton, Michael C. Edwards, Nature Genetics Developmental BiologyMolecular NeuroscienceNeurogenomicsSignal TransductionTgif Cause Holoprosencephaly	2000	390
The Mutational Spectrum of the Sonic Hedgehog Gene in Holoprosencephaly: SHH Mutations Cause a Significant Proportion of Autosomal Dominant Holoprosencephaly Luisa Nanni, Jeffrey E. Ming, Maureen Bocian, Human Molecular Genetics	1999	359
Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects Richard N. Bamford, Erich Roessler, Rebecca D. Burdine, Nature Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsEgf-cfc Gene Cfc1	2000	350
Loss-of-function mutations in the human <i>GLI2</i> gene are associated with pituitary anomalies and holoprosencephaly-like features Erich Roessler, Yangzhu Du, José L. Mullor, Proceedings of the National Academy of Sciences GeneticsMolecular GeneticsDisease Gene IdentificationPituitary AnomaliesMendelian Disorder	2003	344
A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication Mauricio Arcos‐Burgos, Mahim Jain, Maria T. Acosta, Molecular Psychiatry AdhdPsychiatryPsychotropic MedicationPsychopharmacologyStimulant Medication	2010	291

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