Michael A. Morris - Concepedia

Author

Michael A. Morris

Also Known As

Christopher J Mattocks, Francesca Mari, H. Mertes, Inge Liebaers, M A Morris, M Morris, M. A. MORRIS, M. A. Morris, M. Morris, M.A. MORRIS

158

Publications

7.7K

Citations

H-Index

220

Concepts

All Affiliations

University Hospital of Geneva University of Geneva KU Leuven Geneva College Stanford University

About

Michael A. Morris is an author at University Hospital of Geneva specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	8	8	283
2	Health Sciences	4	4	406
3	Education	2	2	135
4	Language Studies	1	1	91
5	Management	1	1	14

Michael A. Morris

Publications

6.9K

Citations

H-Index

Page 1

	Year	Citations
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Maria Karayiorgou, Michael A. Morris, Bernice E. Morrow, Proceedings of the National Academy of Sciences Schizophrenia SusceptibilityPsychiatrySchizophrenia Susceptibility GeneGenetic OverlapGenetics	1995	644
Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy Maria D. Lalioti, Hamish S. Scott, Catherine Burési, Nature Progressive Myoclonus EpilepsyGeneticsNeuroscienceCystatin B GeneNeuropathology	1997	354
Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report Hanan Hamamy, Stylianos E. Antonarakis, Luigi Luca Cavalli-Sforza, Genetics in Medicine Intimate RelationshipGender StudiesSociologyConsanguineous MarriagesForced Marriage	2011	333
COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome Doron Gothelf, Stéphan Eliez, Tracy Thompson, Nature Neuroscience PsychopathologyPsychiatryPsychotic DisorderPsychiatric GeneticsSchizophrenia	2005	319
Enhanced nonenzymatic glucosylation of human serum albumin in diabetes mellitus. C. Earl Guthrow, Michael A. Morris, J.F. Day, Proceedings of the National Academy of Sciences GlycobiologyInsulin SignalingMetabolic SyndromeBioanalysisHematology	1979	265
Schizophrenia: A genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes Ann E. Pulver, Virginia K. Lasseter, Laura Kasch, American Journal of Medical Genetics GeneticsGenetic EpidemiologySusceptibility LociGenome-wide Association StudyGenotype-phenotype Association	1995	254
Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders – updated European recommendations Manfred Stuhrmann, Michael A. Morris, Teresa Casals, European Journal of Human Genetics Genetic DiseasesMedicineGeneticsDiagnosisMolecular Genetic Diagnosis	2008	241
Guidelines for the genetic diagnosis of hereditary recurrent fevers Yael Shinar, Laura Obici, Ivona Aksentijevich, Annals of the Rheumatic Diseases Recurrent BoutsHrf Genetic TestingDisease SusceptibilityGenetic TestingAutoimmune Disease	2012	196
Angelman syndrome due to paternal uniparental disomy of chromosome 15: A milder phenotype? Armand Bottani, Wendy P. Robinson, C.D. DeLozier-Blanchet, American Journal of Medical Genetics	1994	188
Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cells Judith Pratt Rosslter, Michele Young, Michelle L. Kimberland, Human Molecular Genetics Genetic DisorderX ChromosomeGeneticsPathogenesisHematology	1994	179

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