Infant Mortality || Public Health Genomics Knowledge Base (v1.0)

Public Health Genomics Knowledge Base (v1.0)



Infant Mortality

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Last Updated: Feb 03, 2016

• Evidence for an association between infant mortality and homozygosity for the arctic variant of carnitine palmitoyltransferase 1A.
  Gessner Bradford D, et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 1 (From HuGE Literature Finder)
• State Plan for Genetic Services in Missouri[PDF 81.12 KB]
  Disease: Multiple Diseases; Type: Data|Policy|Program; State: Missouri (From Implementation Database)
• Genetic Program Manual for Local Health Departments (August, 2008) (Iowa)[PDF 2.45 MB] 
  Disease: Multiple Diseases; Type: Tools|Program; State: Illinois (From Implementation Database)
• Illinois State Genetics Plan (2007)[PDF 2.04 MB]
  Disease: Multiple Diseases; Type: Policy|Education|Program; State: Illinois (From Implementation Database)
• Connecticut Department of Public Health Genomics Action Plan[PDF 139 KB]
  Disease: Multiple Diseases; Type: Policy|Program; State: Connecticut (From Implementation Database)
• Health policy for sickle cell disease in Africa: experience from Tanzania on interventions to reduce under-five mortality.
  Makani Julie et al. Trop. Med. Int. Health 2015 Feb 20(2) 184-7 (From CDC-Authored Genomics Publication Database)
• Changing Trends in Carrier Screening for Genetic Disease in the United States.
  Nazareth Shivani B et al. Prenat. Diagn. 2015 Jul 3. (From Genomics & Health Impact Scan Database)
• Ethics, genetics and public policies in Uruguay: newborn and infant screening as a paradigm.
  Larrandaburu Mariela et al. J Community Genet 2015 May 29. (From Genomics & Health Impact Scan Database)
• Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings.
  Willig Laurel K et al. Lancet Respir Med 2015 Apr 27. (From Genomics & Health Impact Scan Database)
• The effect of consanguinity on neonatal outcomes and health.
  Abbas Hussein A et al. Hum. Hered. 2014 (1-4) 87-92 (From Discoveries and Insights Database)
• Public health approach to birth defects: the Argentine experience.
  (From Genomics & Health Impact Scan Database)
• Genetic services and testing in South Africa.
  (From Genomics & Health Impact Scan Database)
• The Congenital Heart Disease Genetic Network Study: rationale, design, and early results.
  (From Genomics & Health Impact Scan Database)
• The use of a Toolkit for health needs assessment on neural tube defects in Argentina.
  (From Genomics & Health Impact Scan Database)
• The genomics of preterm birth: from animal models to human studies.
  (From Genomics & Health Impact Scan Database)
• Replication of the 4p16 susceptibility locus in congenital heart disease in Han Chinese populations.
  Zhao Bijun, et al. PloS one 2014 0 (9) e107411 (From HuGE Literature Finder)
• PITX2c loss-of-function mutations responsible for congenital atrial septal defects.
  Yuan Fang, et al. International journal of medical sciences 2013 0 (10) 1422-9 (From HuGE Literature Finder)
• Novel PITX2c loss-of-function mutations associated with complex congenital heart disease.
  Wei Dong, et al. International journal of molecular medicine 2014 5 (5) 1201-8 (From HuGE Literature Finder)
• Spectrum and distribution of CFTR gene mutations in asthma and chronic pancreatitis cases of North Indian population.
  Muthuswamy Srinivasan, et al. Gene 2014 4 (1) 125-31 (From HuGE Literature Finder)
• Association of maternal CNVs in GSTT1/GSTT2 with smoking, preterm delivery, and low birth weight.
  Zheng Xiaojing, et al. Frontiers in genetics 2013 0 196 (From HuGE Literature Finder)