Felicitas Lacbawan - Concepedia

Author

Felicitas Lacbawan

Also Known As

F Lacbawan, F. Lacbawan, F.L. Lacbawan, Felicitas L Lacbawan, Felicitas L. Lacbawan, Felicitas Lacbawan, Mauricio Delgado

Publications

Citations

H-Index

108

Concepts

All Affiliations

National Institutes of Health National Human Genome Research Institute State University of New York Cleveland Clinic Children's National

About

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

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	23	1.7K
2	Public Health	4	4	192
3	Arts	1	1	115
4	Health Sciences	1	1	16
5	Biology	1	1	51

Felicitas Lacbawan

Publications

2.7K

Citations

H-Index

Page 1

	Year	Citations
Familial dementia caused by polymerization of mutant neuroserpin Richard L. Davis, Antony E. Shrimpton, P D Holohan, Nature Alzheimer's DiseaseDementiaFrontotemporal DementiaNeuroscienceNeurology	1999	347
Brain-Derived Neurotrophic Factor and Obesity in the WAGR Syndrome Joan C. Han, Qing‐Rong Liu, MaryPat Jones, New England Journal of Medicine	2008	346
Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly Erich Roessler, Maia V. Ouspenskaia, Jayaprakash D. Karkera, The American Journal of Human Genetics Transcriptional RegulationDevelopmental BiologyNodal Signaling StrengthSignaling PathwayGenetic Disorder	2008	174
Association between conformational mutations in neuroserpin and onset and severity of dementia Richard L. Davis, Antony E. Shrimpton, Robin W. Carrell, The Lancet Alzheimer's DiseaseDementiaGeneticsConformational MutationsVascular Dementia	2002	161
Muenke syndrome (FGFR3‐related craniosynostosis): Expansion of the phenotype and review of the literature Emily S Doherty, Felicitas Lacbawan, Donald W. Hadley, American Journal of Medical Genetics Part A PathologyFgfr3‐related CraniosynostosisPro250arg MutationMendelian DisorderBone Morphogenic Protein	2007	115
Familial Encephalopathy with Neuroserpin Inclusion Bodies Richard L. Davis, P D Holohan, Antony E. Shrimpton, American Journal Of Pathology Neurological DisorderNeuroanatomyNeurologyNeuroscienceBrain Pathology	1999	111
Clinical spectrum of <i>SIX3</i>-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function Felicitas Lacbawan, Benjamin D. Solomon, Erich Roessler, Journal of Medical Genetics	2009	98
The mutational spectrum of holoprosencephaly-associated changes within the<i>SHH</i>gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis Erich Roessler, Kênia Balbi El-Jaick, Christèle Dubourg, Human Mutation GeneticsDisease Gene IdentificationSignaling PathwayHoloprosencephaly-associated ChangesMutational Spectrum	2009	86
Mutations in <i>ZIC2</i> in human holoprosencephaly: description of a Novel <i>ZIC2</i> specific phenotype and comprehensive analysis of 157 individuals B. D. Solomon, Felicitas Lacbawan, Sandra Mercier, Journal of Medical Genetics	2009	83
Traceback: A Proposed Framework to Increase Identification and Genetic Counseling of <i>BRCA1</i> and <i>BRCA2</i> Mutation Carriers Through Family-Based Outreach Goli Samimi, Marcus Q. Bernardini, Lawrence C. Brody, Journal of Clinical Oncology Genetic TestingCancer PathologyGeneticsGenetic EpidemiologyPathology	2017	76

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