Deborah Sival - Concepedia

Author

Deborah Sival

Also Known As

D A Sival, D Sival, D. A. Sival, D. Sival, D.A. Sival, DEBORAH A SIVAL, Deborah A Sival, Deborah A. Sival, Deborah Sival

Publications

829

Citations

H-Index

Concepts

All Affiliations

University Medical Center Groningen University of Groningen Yale University University of California, San Francisco Rutgers, The State University of New Jersey

About

Deborah Sival is an author at University Medical Center Groningen specializing in medicine, health sciences, and pediatrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	416
2	Health Sciences	4	4	126
3	Education	1	1	44
4	Public Health	1	1	15
5	Social Sciences	1	1	44

Deborah Sival

Publications

656

Citations

H-Index

Page 1

	Year	Citations
De Novo Coding Variants Are Strongly Associated with Tourette Disorder A. Jeremy Willsey, Thomas Fernandez, Dongmei Yu, Neuron Tourette DisorderPsychiatryGenetic DisorderGeneticsPsychiatric Genetics	2017	193
Does fetal endoscopic closure of the myelomeningocele prevent loss of neurologic function in spina bifida aperta? R.J. Verbeek, Axel Heep, Natasha M. Maurits, Cerebrospinal Fluid Research Fetal Endoscopic ClosureNeurologic FunctionSpina Bifida ApertaSba ChildrenPediatric Hydrocephalus	2010	84
Neonatal Loss of Motor Function in Human Spina Bifida Aperta Deborah Sival, Tiemen W. van Weerden, Johan S.H. Vles, PEDIATRICS	2004	68
The EEG response to pyridoxine‐IV neither identifies nor excludes pyridoxine‐dependent epilepsy Levinus A. Bok, Natasha M. Maurits, Michèl A.A.P. Willemsen, Epilepsia	2010	65
Shah-Waardenburg syndrome and PCWH associated with SOX10 mutations: A case report and review of the literature Johanna B. G. M. Verheij, Deborah Sival, Johannes H. van der Hoeven, European Journal of Paediatric Neurology Mendelian DisorderDisease MechanismGenetic DisorderMedicineGenetics	2006	58
Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder Mohamed Abdulkadir, Jay A. Tischfield, Robert A. King, Journal of Psychiatric Research AdhdPsychiatryPerinatal ComplicationsPediatricsPsychology	2016	44
Novel homozygous ALS2 nonsense mutation (p.Gln715X) in sibs with infantile-onset ascending spastic paralysis: the first cases from northwestern Europe Corien C. Verschuuren‐Bemelmans, Pia Winter, Deborah Sival, European Journal of Human Genetics First CasesAmyotrophic Lateral SclerosisMendelian DisorderNeurological DisorderGenetic Disorder	2008	40
Pathogenesis of cerebral malformations in human fetuses with meningomyelocele Olga A de Wit, Wilfred F.A. den Dunnen, Krystyne M. Sollie, Cerebrospinal Fluid Research	2008	30
Paediatric motor phenotypes in early‐onset ataxia, developmental coordination disorder, and central hypotonia Tjitske F Lawerman, Rick Brandsma, Natasha M. Maurits, Developmental Medicine & Child Neurology	2019	17
Visual Screening of Muscle Ultrasound Images in Children Rick Brandsma, R.J. Verbeek, Natasha M. Maurits, Ultrasound in Medicine & Biology Medical UltrasoundMedical ImagingPediatricsDiagnosisPaediatric Radiology	2014	16

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