Sarojini Budden - Concepedia

Author

Sarojini Budden

Also Known As

Budden, Sarojini, S BUDDEN, S Budden, S. Budden, S. S. Budden, SAROJINI BUDDEN, Sarojini Budden, Sarojini S Budden, Sarojini S. Budden

Publications

2.5K

Citations

H-Index

Concepts

All Affiliations

Oregon Health & Science University Kennedy Krieger Institute Stanford University University of California, Los Angeles Johns Hopkins University

About

Sarojini Budden is an author at Oregon Health & Science University specializing in medicine, neurology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	15	1.3K
2	Education	3	3	179
3	Social Sciences	3	3	174
4	Health Sciences	2	2	61
5	Public Health	1	1	10

Sarojini Budden

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG Hotspots Mimi Wan, Stephen Sung Jae Lee, Xianyu Zhang, The American Journal of Human Genetics Genome InstabilityRecurrent SpontaneousMendelian DisorderGenetic DisorderRett Syndrome	1999	515
Is angelman syndrome an alternate result of del(15)(qllql3)? R. Ellen Magenis, Michael G. Brown, Deborah A. Lacy, American Journal of Medical Genetics	1987	240
Sleep dysfunction in Rett syndrome: a trial of exogenous melatonin treatment Angela J. McArthur, Sarojini Budden Developmental Medicine & Child Neurology	1998	208
Comparison of the 15q deletions in Prader‐Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences R.E. Magenis, S Toth-Fejel, Leland Allen, American Journal of Medical Genetics	1990	198
Guidelines for reporting clinical features in cases with MECP2 mutations Alison Kerr, Yoshiko Nomura, Dawna Armstrong, Brain and Development Genetic DisorderGeneticsMecp2 MutationsPathologyMedical Genetics	2001	146
<i>FXYD1</i> is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and <i>Mecp2</i>-null mice Vivianne Deng, Valérie Matagne, Fatima Banine, Human Molecular Genetics	2007	145
Qigong Massage Treatment for Sensory and Self-Regulation Problems in Young Children With Autism: A Randomized Controlled Trial Louisa M. T. Silva, Mark Schalock, Robert Ayres, American Journal of Occupational Therapy EducationMotor DifficultyNeurodiversityAutismDevelopmental Disorder	2009	90
Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: Studies in four children Sarojini Budden, Nancy G. Kennaway, Neil R.M. Buist, The Journal of Pediatrics NutritionMetabolic SyndromeMetabolic DisorderMetabolic DiseaseInherited Metabolic Disease	1986	84
Abnormal Expression of Microtubule-Associated Protein 2 (MAP-2) in Neocortex in Rett Syndrome Walter E. Kaufmann, S. Naidu, Sarojini Budden Neuropediatrics Rett SyndromeMicrotubule-associated Protein 2PathologyCellular NeurobiologySynaptic Signaling	1995	76
Ruvalcaba‐myhre‐Smith syndrome: A case with probable autosomal‐dominant inheritance and additional manifestations John H. DiLiberti, Richard G. Weleber, Sarojini Budden, American Journal of Medical Genetics	1983	64

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