Erawati V. Bawle - Concepedia

Author

Erawati V. Bawle

Also Known As

E BAWLE, E V Bawle, E. Bawle, E. V. Bawle, E.V. Bawle, Erawat V. Bawle, Erawati Bawle, Erawati V Bawle, Erawati V. Bawle, Erin Carmany

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

Children's Hospital of Michigan Wayne State University Henry Ford Health System Baylor College of Medicine Signature Research (United States)

About

Erawati V. Bawle is an author at Children's Hospital of Michigan specializing in medicine, pediatrics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	13	886
2	Arts	2	2	144
3	Education	2	2	121
4	Social Sciences	2	2	162
5	Public Health	1	1	107

Erawati V. Bawle

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome Angela L. Duker, Blake C. Ballif, Erawati V. Bawle, European Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathogenesisPathology	2010	316
Hearing, Language, Speech, Vestibular, and Dentofacial Disorders in Fetal Alcohol Syndrome Michael W. Church, Frances Eldis, Brian W. Blakley, Alcoholism Clinical and Experimental Research Dentofacial DisordersPediatric OtolaryngologyAudiologyPediatricsArts	1997	131
Adult and two children with fetal methotrexate syndrome Erawati V. Bawle, J Conard, Lester Weiss Teratology	1998	131
Maternal systemic primary carnitine deficiency uncovered by newborn screening: Clinical, biochemical, and molecular aspects Ayman W. El‐Hattab, Fangyuan Li, Joseph Shen, Genetics in Medicine NutritionNewborn ScreeningPediatricsMaternal HealthMolecular Aspects	2010	107
Memory and Learning in Children with 22q11.2 Deletion Syndrome: Evidence for Ventral and Dorsal Stream Disruption? Renée Lajiness-O’Neill, Isabelle Beaulieu, Jeffrey B. Titus, Child Neuropsychology Developmental Cognitive NeuroscienceEducationDorsal Stream DisruptionHuman MemoryExplicit Memory	2005	103
Transmission of ring chromosome 13 from a mother to daughter with both having a 46,XX, r(13)(p13q34) karyotype Jirair K. Bedoyan, Leigh Anne Flore, Aziz A. Alkatib, American Journal of Medical Genetics Part A Karyotype ImagingChromatinRing Chromosome 13CytogeneticsGenetic Disorder	2004	92
Molecular spectrum of SLC22A5 (OCTN2) gene mutations detected in 143 subjects evaluated for systemic carnitine deficiency Fangyuan Li, Ayman W. El‐Hattab, Erawati V. Bawle, Human Mutation GeneticsMolecular BiologyMolecular GeneticsAbnormal Nbs ResultsGenomics	2010	75
Macrocephaly with hamartomas: Bannayan‐Zonana syndrome Judith H. Miles, Jonathan Zonana, Jean McFarlane, American Journal of Medical Genetics	1984	74
Heterozygous N-terminal deletion of IκBα results in functional nuclear factor κB haploinsufficiency, ectodermal dysplasia, and immune deficiency Douglas R. McDonald, Jana L. Mooster, M.Naveen Kumar Reddy, Journal of Allergy and Clinical Immunology ImmunogeneticsImmune DeficiencyIκbα ResultsHeterozygous N-terminal DeletionDisease Mechanism	2007	74
Medulloblastoma With Adverse Reaction to Radiation Therapy in Nijmegen Breakage Syndrome Sameer Bakhshi, Karen Cerosaletti, Patrick Concannon, Journal of Pediatric Hematology/Oncology Neuro-oncologyRadiation TherapyGliomaGenetic DisorderRadiation Effect	2003	66

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