• Issue

    Birth Defects Research: Volume 114, Issue 20

    1307-1448
    December 1, 2022
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ISSUE INFORMATION

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Issue Information

  • Pages: 1307-1311
  • First Published: December 1, 2022

OPINION

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Viewing teratogens through the lens of nicotinamide adenine dinucleotide (NAD+)

Paul R. Mark,  Sally L. Dunwoodie, 
  • Pages: 1313-1323
  • First Published: 17 September 2022

REVIEW ARTICLES

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Prenatal epigenetic factors are predisposing for neurodevelopmental disorders—Considering placenta as a model

Srividhya Durbagula,  Aruna Korlimarla,  Gayatri Ravikumar,  Snijesh Valiya Parambath,  Sowmyashree Mayur Kaku,  Ashok Mysore Visweswariah, 
  • Pages: 1324-1342
  • First Published: 13 November 2022
Prenatal epigenetic factors are predisposing for neurodevelopmental disorders—Considering placenta as a model

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Delineating septo-optic dysplasia

Mark Lubinsky,  Férechté Encha-Razavi, 
  • Pages: 1343-1353
  • First Published: 06 October 2022

RESEARCH ARTICLES

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Genetic evaluation of HAND2 gene and its effects on thalidomide embryopathy

Bruna Duarte Rengel,  Thayne Woycinck Kowalski,  João Matheus Bremm,  Julia do Amaral Gomes,  Lavínia Schüler-Faccini,  Fernanda Sales Luiz Vianna,  Lucas Rosa Fraga, 
  • Pages: 1354-1363
  • First Published: 30 September 2022
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Reduction of infant mortality from congenital heart defects in a middle-income country: Costa Rican experience

Adriana Benavides-Lara,  María de la Paz Barboza-Argüello,  Olga Arguedas-Arguedas,  Jorge Enrique Faerron-Angel,  Eduardo M. da Cruz, 
  • Pages: 1364-1375
  • First Published: 29 September 2022
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Final results from the ribavirin pregnancy registry, 2004–2020

Susan M. Sinclair,  Judith K. Jones,  Richard K. Miller,  Michael F. Greene,  Paul Y. Kwo,  Willis C. Maddrey, 
  • Pages: 1376-1391
  • First Published: 28 October 2022
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A global update on the status of prevention of folic acid-preventable spina bifida and anencephaly in year 2020: 30-Year anniversary of gaining knowledge about folic acid's prevention potential for neural tube defects

Vijaya Kancherla,  Kaustubh Wagh,  Pretty Priyadarshini,  Helena Pachón,  Godfrey P. Oakley Jr., 
  • Pages: 1392-1403
  • First Published: 07 November 2022
Open Access

Prevalence of congenital heart defects in Europe, 2008–2015: A registry-based study

Chrysovalanto Mamasoula,  Marie-Claude Addor,  Clara Cavero Carbonell,  Carlos M. Dias,  Luis-Javier Echevarría-González-de-Garibay,  Miriam Gatt,  Babak Khoshnood,  Kari Klungsoyr,  Kay Randall,  Sylvia Stoianova,  Martin Haeusler,  Vera Nelen,  Amanda J. Neville,  Isabelle Perthus,  Anna Pierini,  Bénédicte Bertaut-Nativel,  Anke Rissmann,  Florence Rouget,  Bruno Schaub,  David Tucker,  Diana Wellesley,  Natalya Zymak-Zakutnia,  Ingeborg Barisic,  Hermien E. K. de Walle,  Monica Lanzoni,  Carmel Mullaney,  Lindsay Pennington,  Judith Rankin, 
  • Pages: 1404-1416
  • First Published: 08 November 2022
Open Access

Prevalence of vascular disruption anomalies and association with young maternal age: A EUROCAT study to compare the United Kingdom with other European countries

Joan K. Morris,  Diana Wellesley,  Elizabeth Limb,  Jorieke E. H. Bergman,  Agnieszka Kinsner-Ovaskainen,  Marie Claude Addor,  Jennifer M. Broughan,  Clara Cavero-Carbonell,  Carlos M. Dias,  Luis-Javier Echevarría-González-de-Garibay,  Miriam Gatt,  Martin Haeusler,  Ingeborg Barisic,  Kari Klungsoyr,  Nathalie Lelong,  Anna Materna-Kiryluk,  Amanda Neville,  Vera Nelen,  Mary T. O'Mahony,  Isabelle Perthus,  Anna Pierini,  Judith Rankin,  Anke Rissmann,  Florence Rouget,  Geraldine Sayers,  Sarah Stevens,  David Tucker,  Ester Garne, 
  • Pages: 1417-1426
  • First Published: 11 November 2022
Open Access

Amelia and phocomelia in Finland: Characteristics and prevalences in a nationwide population-based study

Niklas Pakkasjärvi,  Johanna Syvänen,  Markus Wiro,  Eeva Koskimies-Virta, 
  • Pages: 1427-1433
  • First Published: 09 November 2022

SHORT COMMUNICATION

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Differential newborn DNA methylation among individuals with complex congenital heart defects and childhood lymphoma

Melissa A. Richard,  Wei Yang,  Pagna Sok,  Ming Li,  Suzan L. Carmichael,  Julie von Behren,  Peggy Reynolds,  Paul G. Fisher,  R. Thomas Collins,  Charlotte A. Hobbs,  Barbara Luke,  Gary M. Shaw,  Philip J. Lupo, 
  • Pages: 1434-1439
  • First Published: 13 October 2022

CASE REPORT

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Clinical and genetic analysis of patients with segmental overgrowth features and somatic mammalian target of rapamycin (mTOR) pathway disruption: Possible novel clinical issues

Ferruccio Romano,  Francesca Madia,  Patrizia De Marco,  Marzia Ognibene,  Sara Guerrisi,  Marcello Scala,  Michele Iacomino,  Simona Baldassari,  Nadia Vercellino,  Francesca Manunza,  Ramona Tallone,  Marco Pavanello,  Gianluca Piatelli,  Alberto Garaventa,  Federico Zara,  Valeria Capra, 
  • Pages: 1440-1448
  • First Published: 08 November 2022