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Mark D. Krieger

University of Southern California · US
Area of research
Genetics · Cellular and Molecular Neuroscience
Research interest
Research interests include Glioma Diagnosis and Treatment, Cerebrospinal fluid and hydrocephalus, Spinal Dysraphism and Malformations, and Fetal and Pediatric Neurological Disorders.
h-index
39
citations
4,456
works
218
NIH funding
primary concept
email

Recent publications

A re-evaluation of the Endoscopic Third Ventriculostomy Success Score: a Hydrocephalus Clinical Research Network study
Journal of Neurosurgery Pediatrics 2024cited by 11position: middledoi
The role of occipital condyle and atlas anomalies on occipital cervical fusion outcomes in Chiari malformation type I with syringomyelia: a study from the Park-Reeves Syringomyelia Research Consortium
Journal of Neurosurgery Pediatrics 2024cited by 9position: middledoi
Comparing ventriculoatrial and ventriculopleural shunts in pediatric hydrocephalus: a Hydrocephalus Clinical Research Network study
Journal of Neurosurgery Pediatrics 2024cited by 7position: middledoi
Does machine learning improve prediction accuracy of the Endoscopic Third Ventriculostomy Success Score? A contemporary Hydrocephalus Clinical Research Network cohort study
Child s Nervous System 2024cited by 2position: middledoi
Complications and outcomes of posterior fossa decompression with duraplasty versus without duraplasty for pediatric patients with Chiari malformation type I and syringomyelia: a study from the Park-Reeves Syringomyelia Research Consortium
Journal of Neurosurgery Pediatrics 2022cited by 39position: middledoi
Endoscopic third ventriculostomy in previously shunt-treated patients
Journal of Neurosurgery Pediatrics 2022cited by 18position: middledoi
Dural augmentation approaches and complication rates after posterior fossa decompression for Chiari I malformation and syringomyelia: a Park-Reeves Syringomyelia Research Consortium study
Journal of Neurosurgery Pediatrics 2021cited by 30position: middledoi
Treatment strategies for hydrocephalus related to Dandy-Walker syndrome: evaluating procedure selection and success within the Hydrocephalus Clinical Research Network
Journal of Neurosurgery Pediatrics 2021cited by 22position: middledoi
Extradural decompression versus duraplasty in Chiari malformation type I with syrinx: outcomes on scoliosis from the Park-Reeves Syringomyelia Research Consortium
Journal of Neurosurgery Pediatrics 2021cited by 16position: middledoi
Occipital-Cervical Fusion and Ventral Decompression in the Surgical Management of Chiari-1 Malformation and Syringomyelia: Analysis of Data From the Park-Reeves Syringomyelia Research Consortium
Neurosurgery 2020cited by 28position: middledoi
Surgical resource utilization after initial treatment of infant hydrocephalus: comparing ETV, early experience of ETV with choroid plexus cauterization, and shunt insertion in the Hydrocephalus Clinical Research Network
Journal of Neurosurgery Pediatrics 2020cited by 25position: middledoi
Predictors of fast and ultrafast shunt failure in pediatric hydrocephalus: a Hydrocephalus Clinical Research Network study
Journal of Neurosurgery Pediatrics 2020cited by 22position: middledoi
Editorial. Early lessons in the management of COVID-19 for the pediatric neurosurgical community from the leadership of the American Society of Pediatric Neurosurgeons
Journal of Neurosurgery Pediatrics 2020cited by 21position: middledoi
Radiological and clinical predictors of scoliosis in patients with Chiari malformation type I and spinal cord syrinx from the Park-Reeves Syringomyelia Research Consortium
Journal of Neurosurgery Pediatrics 2019cited by 18position: middledoi
Prospective feasibility and safety assessment of surgical biopsy for patients with newly diagnosed diffuse intrinsic pontine glioma
Neuro-Oncology 2018cited by 133position: middledoi
PDCT-20. FEASIBILITY AND SAFETY OF SURGICAL BIOPSY FOR PATIENTS WITH DIPG: PRELIMINARY RESULTS FROM DIPG-BATS
Neuro-Oncology 2017cited by 1position: middledoi
A retrospective analysis of recurrent intracranial ependymoma
Pediatric Blood & Cancer 2014cited by 46position: middledoi
<i>PID1</i> ( <i>NYGGF4</i> ), a New Growth-Inhibitory Gene in Embryonal Brain Tumors and Gliomas
Clinical Cancer Research 2013cited by 34position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

John C. Wellons · Monroe Carell Jr. Children's Hospital7 papers (2020–2024)David D. Limbrick · Virginia Commonwealth University6 papers (2020–2024)Jay Riva-Cambrin · University of Calgary6 papers (2020–2024)John R. W. Kestle · Primary Children's Hospital6 papers (2020–2024)Ian F. Pollack · University of Pittsburgh6 papers (2020–2024)Todd C. Hankinson · University of Colorado Denver6 papers (2020–2024)Patrick J. McDonald · Seattle Children's Hospital6 papers (2020–2024)Mandeep S. Tamber · University of Illinois Chicago6 papers (2020–2024)Ron Reeder · University of Utah6 papers (2020–2024)Eric M. Jackson · Johns Hopkins University6 papers (2020–2024)Jason S. Hauptman · Seattle Children's Hospital6 papers (2020–2024)Jonathan Pindrik · University of Alabama at Birmingham6 papers (2020–2024)Abhaya V. Kulkarni · University of Toronto6 papers (2020–2024)William E. Whitehead · University of North Carolina at Chapel Hill5 papers (2020–2024)Hailey Jensen · University of Utah4 papers (2021–2024)Jason Chu · Columbia University Irving Medical Center4 papers (2020–2024)Robert P. Naftel · Monroe Carell Jr. Children's Hospital4 papers (2020–2022)Curtis J. Rozzelle · Children's of Alabama4 papers (2020–2022)Brandon G. Rocque · Children's of Alabama3 papers (2022–2024)Samuel R. Browd · Neurological Surgery3 papers (2020–2024)