Sudden infant death syndrome: study of genes pertinent to cardiorespiratory and autonomic regulation

[1]  D. Tester,et al.  A mechanism for sudden infant death syndrome (SIDS): stress-induced leak via ryanodine receptors. , 2007, Heart rhythm.

[2]  Michael J Ackerman,et al.  Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3. , 2007, Heart rhythm.

[3]  Dan M Roden,et al.  Cardiac potassium channel dysfunction in sudden infant death syndrome. , 2007, Journal of molecular and cellular cardiology.

[4]  Peter J. Schwartz,et al.  Prevalence of Long-QT Syndrome Gene Variants in Sudden Infant Death Syndrome , 2007, Circulation.

[5]  S. Priori,et al.  Cost-effectiveness of neonatal ECG screening for the long QT syndrome. , 2006, European heart journal.

[6]  E. Berry-Kravis,et al.  Congenital central hypoventilation syndrome: PHOX2B mutations and phenotype. , 2006, American journal of respiratory and critical care medicine.

[7]  Michael J Ackerman,et al.  Mutant Caveolin-3 Induces Persistent Late Sodium Current and Is Associated With Long-QT Syndrome , 2006, Circulation.

[8]  Amy E. Chadwick,et al.  Multiple serotonergic brainstem abnormalities in sudden infant death syndrome. , 2006, JAMA.

[9]  B. Maher,et al.  Sudden infant death syndrome: Case‐control frequency differences in paired like homeobox (PHOX) 2B gene , 2006, American journal of medical genetics. Part A.

[10]  W. Budts,et al.  Prevalence of cardiovascular risk factors in adults with congenital heart disease , 2006, European journal of cardiovascular prevention and rehabilitation : official journal of the European Society of Cardiology, Working Groups on Epidemiology & Prevention and Cardiac Rehabilitation and Exercise Physiology.

[11]  B. Maher,et al.  3′ UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: Haplotype analysis , 2006, American journal of medical genetics. Part A.

[12]  B. Maher,et al.  Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndrome , 2006, American journal of medical genetics. Part A.

[13]  S. L. Murphy,et al.  Deaths: final data for 2003. , 2006, National vital statistics reports : from the Centers for Disease Control and Prevention, National Center for Health Statistics, National Vital Statistics System.

[14]  Matthew W State,et al.  A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y. , 2006, The Journal of clinical investigation.

[15]  D. Tester,et al.  Sudden infant death syndrome: how significant are the cardiac channelopathies? , 2005, Cardiovascular research.

[16]  P. Sham,et al.  The serotonin transporter gene as a QTL for ADHD , 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[17]  A. Munnich,et al.  PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndrome. , 2005, American journal of human genetics.

[18]  Jørgen K. Kanters,et al.  Mutations in the HERG K+-ion channel: a novel link between long QT syndrome and sudden infant death syndrome. , 2005, The American journal of cardiology.

[19]  Johnf . Thompson,et al.  Role of a KCNH2 polymorphism (R1047 L) in dofetilide-induced Torsades de Pointes. , 2004, Journal of molecular and cellular cardiology.

[20]  J. Stephens,et al.  Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing. , 2004, Heart rhythm.

[21]  Lili Zhou,et al.  Sudden Infant Death Syndrome: Case-Control Frequency Differences at Genes Pertinent to Early Autonomic Nervous System Embryologic Development , 2004, Pediatric Research.

[22]  François Guillemot,et al.  Ascl1/Mash1 is required for the development of central serotonergic neurons , 2004, Nature Neuroscience.

[23]  M. Ackerman,et al.  Cardiac channelopathies: it's in the genes , 2004, Nature Medicine.

[24]  K. Hayasaka,et al.  Sudden infant death syndrome is not associated with the mutation of PHOX2B gene, a major causative gene of congenital central hypoventilation syndrome. , 2004, The Tohoku journal of experimental medicine.

[25]  R. Ravazzolo,et al.  PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome , 2004, Journal of Medical Genetics.

[26]  B. Maher,et al.  Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b , 2003, American journal of medical genetics. Part A.

[27]  Michael J Ackerman,et al.  Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome. , 2003, Mayo Clinic proceedings.

[28]  H. Kinney,et al.  Serotonergic Brainstem Abnormalities in Northern Plains Indians with the Sudden Infant Death Syndrome , 2003, Journal of neuropathology and experimental neurology.

[29]  Tomohiko Nakamura,et al.  Molecular analysis of congenital central hypoventilation syndrome , 2003, Human Genetics.

[30]  B. Maher,et al.  Association of the serotonin transporter gene with sudden infant death syndrome: A haplotype analysis , 2003, American journal of medical genetics. Part A.

[31]  M. Garcia-Barceló,et al.  Association study of PHOX2B as a candidate gene for Hirschsprung’s disease , 2003, Gut.

[32]  R. Rosmond,et al.  Serotonin transporter gene polymorphisms and platelet [3H] paroxetine binding in premenstrual dysphoria , 2003, Psychoneuroendocrinology.

[33]  A. Munnich,et al.  Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome , 2003, Nature Genetics.

[34]  R. Krumlauf,et al.  Coordinated temporal and spatial control of motor neuron and serotonergic neuron generation from a common pool of CNS progenitors. , 2003, Genes & development.

[35]  B. Maher,et al.  Sudden infant death syndrome: Association with a promoter polymorphism of the serotonin transporter gene , 2003, American journal of medical genetics. Part A.

[36]  V. Bubb,et al.  The serotonin transporter intronic VNTR enhancer correlated with a predisposition to affective disorders has distinct regulatory elements within the domain based on the primary DNA sequence of the repeat unit , 2003, The European journal of neuroscience.

[37]  M. Egan,et al.  Serotonin Transporter Genetic Variation and the Response of the Human Amygdala , 2002, Science.

[38]  N. Okado,et al.  Alteration of serotonergic receptors in the brain stems of human patients with respiratory disorders. , 2002, Neuropediatrics.

[39]  Tianhua Niu,et al.  Maternal cigarette smoking, metabolic gene polymorphism, and infant birth weight. , 2002, JAMA.

[40]  J. Towbin,et al.  Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome. , 2001, JAMA.

[41]  G. Breithardt,et al.  Molecular diagnosis in a child with sudden infant death syndrome , 2001, The Lancet.

[42]  A. Miniño,et al.  Deaths: preliminary data for 2000. , 2001, National vital statistics reports : from the Centers for Disease Control and Prevention, National Center for Health Statistics, National Vital Statistics System.

[43]  K R Nielsen,et al.  Acute exposure to environmental tobacco smoke and heart rate variability. , 2001, Environmental health perspectives.

[44]  M. Yanagisawa,et al.  Impaired Ventilatory Responses to Hypoxia in Mice Deficient in Endothelin-Converting-Enzyme-1 , 2001, Pediatric Research.

[45]  B. Maher,et al.  Case/control family study of autonomic nervous system dysfunction in idiopathic congenital central hypoventilation syndrome. , 2001, American journal of medical genetics.

[46]  B. Maher,et al.  Genetic segregation analysis of autonomic nervous system dysfunction in families of probands with idiopathic congenital central hypoventilation syndrome. , 2001, American journal of medical genetics.

[47]  S. Takashima,et al.  Serotonin Transporter Gene Variation Is a Risk Factor for Sudden Infant Death Syndrome in the Japanese Population , 2001, Pediatrics.

[48]  G. Breithardt,et al.  Life-threatening Arrhythmias Genotype-phenotype Correlation in the Long-qt Syndrome : Gene-specific Triggers for Genotype-phenotype Correlation in the Long-qt Syndrome Gene-specific Triggers for Life-threatening Arrhythmias , 2022 .

[49]  P. Hrdina,et al.  Gender differences in association between serotonin transporter gene polymorphism and personality traits. , 2000, Psychiatric genetics.

[50]  S. Priori,et al.  A molecular link between the sudden infant death syndrome and the long-QT syndrome. , 2000, The New England journal of medicine.

[51]  H. Kinney,et al.  Decreased Serotonergic Receptor Binding in Rhombic Lip‐Derived Regions of the Medulla Oblongata in the Sudden Infant Death Syndrome , 2000, Journal of neuropathology and experimental neurology.

[52]  Andreas Heinz,et al.  A relationship between serotonin transporter genotype and in vivo protein expression and alcohol neurotoxicity , 2000, Biological Psychiatry.

[53]  B. Greenberg,et al.  Interaction between the serotonin transporter gene and neuroticism in cigarette smoking behavior , 2000, Molecular Psychiatry.

[54]  Y. Osher,et al.  Association and linkage of anxiety-related traits with a functional polymorphism of the serotonin transporter gene regulatory region in Israeli sibling pairs , 2000, Molecular Psychiatry.

[55]  S. Korsmeyer,et al.  Rnx deficiency results in congenital central hypoventilation , 2000, Nature Genetics.

[56]  P. Franco,et al.  Influence of Maternal Smoking on Autonomic Nervous System in Healthy Infants , 2000, Pediatric Research.

[57]  F. Zhou,et al.  Expression of serotonin transporter protein in developing rat brain. , 2000, Brain research. Developmental brain research.

[58]  J. Quinn,et al.  A serotonin transporter gene intron 2 polymorphic region, correlated with affective disorders, has allele-dependent differential enhancer-like properties in the mouse embryo. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[59]  D. Tester,et al.  Swimming, a gene-specific arrhythmogenic trigger for inherited long QT syndrome. , 1999, Mayo Clinic proceedings.

[60]  S. Priori,et al.  Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome. , 1999, The American journal of cardiology.

[61]  C. Fiskerstrand,et al.  An intronic polymorphic domain often associated with susceptibility to affective disorders has allele dependent differential enhancer activity in embryonic stem cells , 1999, FEBS letters.

[62]  T. Arinami,et al.  Association between drinking-related antisocial behavior and a polymorphism in the serotonin transporter gene in a Japanese population. , 1999, Alcoholism, clinical and experimental research.

[63]  P. Franco,et al.  Decreased Autonomic Responses to Obstructive Sleep Events in Future Victims of Sudden Infant Death Syndrome , 1999, Pediatric Research.

[64]  X. Morin,et al.  The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives , 1999, Nature.

[65]  D. Blackwood,et al.  Presence of Multiple Functional Polyadenylation Signals and a Single Nucleotide Polymorphism in the 3′ Untranslated Region of the Human Serotonin Transporter Gene , 1999, Journal of neurochemistry.

[66]  David J. Anderson,et al.  Specification of Neurotransmitter Identity by Phox2 Proteins in Neural Crest Stem Cells , 1999, Neuron.

[67]  K K Kidd,et al.  Population studies of polymorphisms of the serotonin transporter protein gene. , 1999, American journal of medical genetics.

[68]  Hiroshi Kunugi,et al.  Association between serotonin transporter gene polymorphism and anxiety-related traits , 1999, Biological Psychiatry.

[69]  R. Hauer,et al.  Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1). , 1999, Journal of the American College of Cardiology.

[70]  L. Siever,et al.  Serotonin transporter protein gene polymorphism and personality measures in African American and European American subjects. , 1998, The American journal of psychiatry.

[71]  D. Kupfer,et al.  How common is resistance to treatment in recurrent, nonpsychotic geriatric depression? , 1998, The American journal of psychiatry.

[72]  P. Schwartz,et al.  Prolongation of the QT interval and the sudden infant death syndrome. , 1998, The New England journal of medicine.

[73]  M. Ledwidge,et al.  Neurocardiogenic syncope: a model for SIDS , 1998, Archives of disease in childhood.

[74]  P. Shields,et al.  The role of the serotonin transporter gene in cigarette smoking. , 1998, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[75]  M. Hirsch,et al.  Control of noradrenergic differentiation and Phox2a expression by MASH1 in the central and peripheral nervous system. , 1998, Development.

[76]  D. Anderson,et al.  MASH1 activates expression of the paired homeodomain transcription factor Phox2a, and couples pan-neuronal and subtype-specific components of autonomic neuronal identity. , 1998, Development.

[77]  E H Cook,et al.  Cocaine, ethanol, and genotype effects on human midbrain serotonin transporter binding sites and mRNA levels. , 1998, The American journal of psychiatry.

[78]  M. Spitz,et al.  Susceptibility to lung cancer in light smokers associated with CYP1A1 polymorphisms in Mexican- and African-Americans. , 1997, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[79]  D. Cook,et al.  Passive smoking and sudden infant death syndrome: review of the epidemiological evidence. , 1997, Thorax.

[80]  E. Mitchell,et al.  Risk factors for sudden infant death syndrome following the prevention campaign in New Zealand: a prospective study. , 1997, Pediatrics.

[81]  X. Morin,et al.  Expression and interactions of the two closely related homeobox genes Phox2a and Phox2b during neurogenesis. , 1997, Development.

[82]  P. Blair,et al.  Giving thyroid hormones to clinically hypothyroid but biochemically euthyroid patients , 1997, BMJ.

[83]  S. Kanba,et al.  Serotonin transporter gene regulatory region polymorphism and anxiety-related traits in the Japanese. , 1997, American journal of medical genetics.

[84]  H. Hoffman,et al.  Sudden infant death syndrome and smoking in the United States and Sweden. , 1997, American journal of epidemiology.

[85]  G. Brüning,et al.  Prenatal development of the serotonin transporter in mouse brain , 1997, Cell and Tissue Research.

[86]  H. Brown,et al.  Case-control study of sudden infant death syndrome in Scotland, 1992-5 , 1997, BMJ.

[87]  D. Shannon,et al.  RET proto-oncogene is important for the development of respiratory CO2 sensitivity. , 1997, Journal of the autonomic nervous system.

[88]  R. Murray,et al.  A novel functional polymorphism within the promoter of the serotonin transporter gene: possible role in susceptibility to affective disorders. , 1996, Molecular psychiatry.

[89]  K. Lesch,et al.  Association of Anxiety-Related Traits with a Polymorphism in the Serotonin Transporter Gene Regulatory Region , 1996, Science.

[90]  E. Mitchell,et al.  Symptoms, sweating and reactivity of infants who die of SIDS compared with community controls , 1996, Journal of paediatrics and child health.

[91]  P. J. Fleming,et al.  Smoking and the sudden infant death syndrome: results from 1993-5 case-control study for confidential inquiry into stillbirths and deaths in infancy , 1996 .

[92]  R. Murray,et al.  The serotonin transporter is a potential susceptibility factor for bipolar affective disorder. , 1996, Neuroreport.

[93]  P Riederer,et al.  Allelic Variation of Human Serotonin Transporter Gene Expression , 1996, Journal of neurochemistry.

[94]  A Malliani,et al.  A controlled study of the autonomic changes produced by habitual cigarette smoking in healthy subjects. , 1996, Cardiovascular research.

[95]  G. Goodwin,et al.  Polymorphism in serotonin transporter gene associated with susceptibility to major depression , 1996, The Lancet.

[96]  J. Lauder,et al.  Serotonin regulates mouse cranial neural crest migration. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[97]  M. Kotamäki Smoking induced differences in autonomic responses in military pilot candidates , 1995, Clinical Autonomic Research.

[98]  S. Piha Cardiovascular autonomic reflexes in heavy smokers. , 1994, Journal of the autonomic nervous system.

[99]  Mary T. Carbone,et al.  Cardiorespiratory recordings from infants dying suddenly and unexpectedly at home. , 1994, Pediatrics.

[100]  M. Marazita,et al.  Congenital central hypoventilation syndrome: inheritance and relation to sudden infant death syndrome. , 1993, American journal of medical genetics.

[101]  D L Eckberg,et al.  Influence of Cigarette Smoking on Human Autonomic Function , 1993, Circulation.

[102]  K. Nakachi,et al.  Polymorphisms of the CYP1A1 and glutathione S-transferase genes associated with susceptibility to lung cancer in relation to cigarette dose in a Japanese population. , 1993, Cancer research.

[103]  R. Blakely,et al.  Antidepressant- and cocaine-sensitive human serotonin transporter: molecular cloning, expression, and chromosomal localization. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[104]  K. Kawajiri,et al.  High Susceptibility to Lung Cancer Analyzed in Terms of Combined Genotypes of P450IA1 and Mu‐class Glutathione S‐Transferase Genes , 1992, Japanese journal of cancer research : Gann.

[105]  J. Groswasser,et al.  Sleep and cardiorespiratory characteristics of infant victims of sudden death: a prospective case-control study. , 1992, Sleep.

[106]  T. Dwyer,et al.  Thermal environment and sudden infant death syndrome: case-control study. , 1992, BMJ.

[107]  R. Gilbert,et al.  Interaction between bedding and sleeping position in the sudden infant death syndrome: a population based case-control study. , 1990, BMJ.

[108]  H. Hoffman,et al.  Cardiac and respiratory patterns in normal infants and victims of the sudden infant death syndrome. , 1988, Sleep.

[109]  B. Maron,et al.  Potential Role of QT Interval Prolongation in Sudden Infant Death Syndrome , 1976, Circulation.

[110]  P. Schwartz Cardiac sympathetic innervation and the sudden infant death syndrome. A possible pathogenetic link. , 1976, The American journal of medicine.

[111]  P. Riederer,et al.  Organization of the human serotonin transporter gene , 2005, Journal of Neural Transmission / General Section JNT.

[112]  H. Bartsch,et al.  Genetic polymorphism of CYP genes, alone or in combination, as a risk modifier of tobacco-related cancers. , 2000, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[113]  D. Shannon,et al.  Idiopathic congenital central hypoventilation syndrome: diagnosis and management. American Thoracic Society. , 1999, American journal of respiratory and critical care medicine.

[114]  J. A. Martin,et al.  ADVANCE REPORT OF FINAL NATALITY STATISTIC, 1992 , 1994 .

[115]  H. Kinney,et al.  A perspective on neuropathologic findings in victims of the sudden infant death syndrome: the triple-risk model. , 1994, Biology of the neonate.

[116]  B. Jacobs,et al.  Structure and function of the brain serotonin system. , 1992, Physiological reviews.