Dr. Hannah Kinney

Hannah C. Kinney, M.D.

617-355-6330
Harvard Catalyst Profile
Harvard Title

Professor of Pathology, Emerita

Other Affiliations

Boston Children's Hospital

Address

Childrens Hospital
Neuroscience
300 Longwood Ave  
Boston MA 02115

Publications View
Consent for autopsy research for unexpected death in early life.
Authors: Odendaal HJ, Elliott A, Kinney HC, Human M, Gaspar D, Petersen D, Randall B, Dempers J.
Obstet Gynecol
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Lack of association of the serotonin transporter polymorphism with the sudden infant death syndrome in the San Diego Dataset.
Authors: Paterson DS, Rivera KD, Broadbelt KG, Trachtenberg FL, Belliveau RA, Holm IA, Haas EA, Stanley C, Krous HF, Kinney HC, Markianos K.
Pediatr Res
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The cerebral cortex overlying periventricular leukomalacia: analysis of pyramidal neurons.
Authors: Andiman SE, Haynes RL, Trachtenberg FL, Billiards SS, Folkerth RD, Volpe JJ, Kinney HC.
Brain Pathol
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Neuroanatomic relationships between the GABAergic and serotonergic systems in the developing human medulla.
Authors: Broadbelt KG, Paterson DS, Rivera KD, Trachtenberg FL, Kinney HC.
Auton Neurosci
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Brainstem serotonergic deficiency in sudden infant death syndrome.
Authors: Duncan JR, Paterson DS, Hoffman JM, Mokler DJ, Borenstein NS, Belliveau RA, Krous HF, Haas EA, Stanley C, Nattie EE, Trachtenberg FL, Kinney HC.
JAMA
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Novel neuropathologic findings in the Haddad syndrome.
Authors: Tomycz ND, Haynes RL, Schmidt EF, Ackerson K, Kinney HC.
Acta Neuropathol
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Potential Mechanisms of Failure in the Sudden Infant Death Syndrome.
Authors: Harper RM, Kinney HC.
Curr Pediatr Rev
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The encephalopathy of prematurity: one pediatric neuropathologist's perspective.
Authors: Kinney HC.
Semin Pediatr Neurol
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A practical classification schema incorporating consideration of possible asphyxia in cases of sudden unexpected infant death.
Authors: Randall BB, Wadee SA, Sens MA, Kinney HC, Folkerth RD, Odendaal HJ, Dempers JJ.
Forensic Sci Med Pathol
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Serotonin-related FEV gene variant in the sudden infant death syndrome is a common polymorphism in the African-American population.
Authors: Broadbelt KG, Barger MA, Paterson DS, Holm IA, Haas EA, Krous HF, Kinney HC, Markianos K, Beggs AH.
Pediatr Res
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