Joanne Weinberg

Dr. Joanne Weinberg

orcid

Research Focus & Metrics

Academic Career Length

50Years (1977-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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24 March 2008 in Epigenetics
Verified
Journal Article
Closed access
TOTim F. Oberlander
Tim F. Oberlander
JWJoanne Weinberg
Joanne Weinberg
MPMichael Papsdorf
Michael Papsdorf
RGRuth Grunau
Ruth Grunau
SMShaila Misri
Shaila Misri
ADAngela Devlin
Angela Devlin
Background: In animal models, variations in early maternal care are associated with differences in hypothalamic-pituitary-adrenal (HPA) stress response in the offspring, mediated via changes in the...

1 October 2012 in Neuroscience & Biobehavioral Reviews
Verified
Journal Article
Closed access
MHMatthew N. Hill
Matthew N. Hill
KHKim G.C. Hellemans
Kim G.C. Hellemans
PVPamela Verma
Pamela Verma
BGBoris B. Gorzalka
Boris B. Gorzalka
JWJoanne Weinberg
Joanne Weinberg

1 February 2005 in Pain
Verified
Journal Article
Closed access
RGRuth E. Grunau
Ruth E. Grunau
LHLiisa Holsti
Liisa Holsti
DHDavid W. Haley
David W. Haley
TOTim F. Oberlander
Tim F. Oberlander
JWJoanne Weinberg
Joanne Weinberg
WYWayne Yu
Wayne Yu
Data from animal models indicate that neonatal stress or pain can permanently alter subsequent behavioral and/or physiological reactivity to stressors. However, cumulative effects of pain related to acute procedures in the neonatal intensive care unit (NICU) on later stress and/or pain reactivity has received limited attention. The objective of this study is to examine relationships between prior neonatal pain exposure (number of skin breaking procedures), and subsequent stress and pain reactivity in preterm infants in the NICU. Eighty-seven preterm infants were studied at 32 (+/-1 week) postconceptional age (PCA). Infants who received analgesia or sedation in the 72 h prior to each study, or any postnatal dexamethasone, were excluded. Outcomes were infant responses to two different stressors studied on separate days in a repeated measures randomized crossover design: (1) plasma cortisol to stress of a fixed series of nursing procedures; (2) behavioral (Neonatal Facial Coding System; NFCS) and cardiac reactivity to pain of blood collection. Among infants born <or=28 weeks gestational age (GA), but not 29-32 weeks GA, higher cumulative neonatal procedural pain exposure was related to lower cortisol response to stress and to lower facial (but not autonomic) reactivity to pain, at 32 weeks PCA, independent of early illness severity and morphine exposure since birth. Repeated neonatal procedural pain exposure among neurodevelopmentally immature preterm infants was associated with down-regulation of the hypothalamic-pituitary-adrenal axis, which was not counteracted with morphine. Differential effects of early pain on development of behavioral, physiologic and hormonal systems warrant further investigation.

1 May 2010 in Neuroscience & Biobehavioral Reviews
Verified
Journal Article
Closed access
KHKim G.C. Hellemans
Kim G.C. Hellemans
JSJoanna H. Sliwowska
Joanna H. Sliwowska
PVPamela Verma
Pamela Verma
JWJoanne Weinberg
Joanne Weinberg

8 February 2008 in Journal of Neuroendocrinology
Verified
Journal Article
Closed access
PDF file
JWJoanne Weinberg
Joanne Weinberg
JSJ. H. Sliwowska
J. H. Sliwowska
NLN. Lan
N. Lan
KHK. G. C. Hellemans
K. G. C. Hellemans

1 February 2007 in The Journal of Pediatrics
Verified
Journal Article
Closed access
RGRuth E. Grunau
Ruth E. Grunau
DHDavid W. Haley
David W. Haley
MWMichael F. Whitfield
Michael F. Whitfield
JWJoanne Weinberg
Joanne Weinberg
WYWayne Yu
Wayne Yu
PTPaul Thiessen
Paul Thiessen