Physician
Medical Genetics
Dr. Edward J. Lammer, MD
|
|
Give Review
Edward Lammer works in the field of Medical Genetics. He researched medicine at University of Iowa Carver College of Medicine. University of Iowa Carver College of Medicine has a rank of 29 in research and a 16 in primary care He received awards:"Fellow (FAAP)". Edward J. Lammer is a published MD. He has 74 publications published. The most current publication "Craniosynostosis and risk factors related to thyroid dysfunction."
Publications
- Craniosynostosis and risk factors related to thyroid dysfunction.
- One-carbon metabolite levels in mid-pregnancy and risks of conotruncal heart defects.
- Hypospadias and variants in genes related to sex hormone biosynthesis and metabolism.
- Hypospadias and Residential Proximity to Pesticide Applications.
- Identification of novel candidate gene loci and increased sex chromosome aneuploidy among infants with conotruncal heart defects.
- Congenital heart defects after maternal fever.
- Hypospadias and Genes Related to Genital Tubercle and Early Urethral Development.
- Considering the vascular hypothesis for the pathogenesis of small intestinal atresia: A case control study of genetic factors.
- Thymidylate synthase polymorphisms and risks of human orofacial clefts.
- Diacylglycerol kinase k variants impact hypospadias in a california study population.
- Environmental and genetic contributors to hypospadias: A review of the epidemiologic evidence.
- A genetic signature of spina bifida risk from pathway-informed comprehensive gene-variant analysis.
- Periconceptional nutrient intakes and risks of conotruncal heart defects.
- Planar cell polarity pathway genes and risk for spina bifida.
- Association of congenital cardiovascular malformations with 33 single nucleotide polymorphisms of selected cardiovascular disease-related genes.
- Genetic polymorphisms in the thioredoxin 2 (TXN2) gene and risk for spina bifida.
- Chromosomal abnormalities among children born with conotruncal cardiac defects.
- Nicotinamide N-methyl transferase (NNMT) gene polymorphisms and risk for spina bifida.
- Genetic susceptibilities in the association between maternal exposure to tobacco smoke and the risk of nonsyndromic oral cleft.
- Gastroschisis: a gene-environment model involving the VEGF-NOS3 pathway.
- Maternal periconceptional smoking and alcohol consumption and risk for select congenital anomalies.
- NAT2 variation and idiopathic talipes equinovarus (clubfoot).
- Association between 49 infant gene polymorphisms and preterm delivery.
- Maternal smoking during early pregnancy, GSTP1 and EPHX1 variants, and risk of isolated orofacial clefts.
- Comprehensive EMX2 genotyping of a large schizencephaly case series.
- Ovotestes and XY sex reversal in a female with an interstitial 9q33.3-q34.1 deletion encompassing NR5A1 and LMX1B causing features of Genitopatellar syndrome.
- Maternal stressful life events and risks of birth defects.
- Maternal smoking and environmental tobacco smoke exposure and the risk of orofacial clefts.
- Association between a leukotriene C4 synthase gene promoter polymorphism and coronary artery calcium in young women: the Muscatine Study.
- Screening for novel PAX3 polymorphisms and risks of spina bifida.
- Risks of human limb deficiency anomalies associated with 29 SNPs of genes involved in homocysteine metabolism, coagulation, cell-cell interactions, inflammatory respon...
- Candidate gene polymorphisms do not differ between newborns with stroke and normal controls.
- Selected gene polymorphisms and their interaction with maternal smoking, as risk factors for gastroschisis.
- Phosphatidylethanolamine N-methyltransferase (PEMT) gene polymorphisms and risk of spina bifida.
- Patterns of infantile hemangiomas: new clues to hemangioma pathogenesis and embryonic facial development.
- A known functional polymorphism (Ile120Val) of the human PCMT1 gene and risk of spina bifida.
- Endothelial nitric oxide synthase (NOS3) genetic variants, maternal smoking, vitamin use, and risk of human orofacial clefts.
- Genetic variation in the proto-oncogene SKI and risk for orofacial clefting.
- Maternal progestin intake and risk of hypospadias.
- Risks of human conotruncal heart defects associated with 32 single nucleotide polymorphisms of selected cardiovascular disease-related genes.
- Maternal smoking, genetic variation of glutathione s-transferases, and risk for orofacial clefts.
- Genes encoding catalytic subunits of protein kinase A and risk of spina bifida.
- Schizencephaly: heterogeneous etiologies in a population of 4 million California births.
- Epidemiologic characteristics of anophthalmia and bilateral microphthalmia among 2.5 million births in California, 1989-1997.
- Are the betaine-homocysteine methyltransferase (BHMT and BHMT2) genes risk factors for spina bifida and orofacial clefts?
- Periconceptional multivitamin intake during early pregnancy, genetic variation of acetyl-N-transferase 1 (NAT1), and risk for orofacial clefts.
- Lacrimoauriculodentodigital syndrome with cleft lip/palate and renal manifestations.
- Embryonic development of folate binding protein-1 (Folbp1) knockout mice: Effects of the chemical form, dose, and timing of maternal folate supplementation.
- Gene-nutrient interactions: importance of folates and retinoids during early embryogenesis.
- Evaluation of the Cited2 gene and risk for spina bifida and congenital heart defects.
- Evaluation of the jumonji gene and risk for spina bifida and congenital heart defects.
- Limb deficiency defects, MSX1, and exposure to tobacco smoke.
- Congenital malformations in births with orofacial clefts among 3.6 million California births, 1983-1997.
- Maternal smoking and the risk of orofacial clefts: Susceptibility with NAT1 and NAT2 polymorphisms.
- Promoter haplotype combinations for the human PDGFRA gene are associated with risk of neural tube defects.
- Autosomal recessive frontotemporal pachygyria.
- Associations between polymorphisms within the thymidylate synthase gene and spina bifida.
- Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial and conotruncal heart defects.
- Maternal periconceptional alcohol consumption and risk for conotruncal heart defects.
- Maternal occupational chemical exposures and biotransformation genotypes as risk factors for selected congenital anomalies.
- Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects.
- Risk factors for neural tube defects: associations between uncoupling protein 2 polymorphisms and spina bifida.
- Evaluation of infant methylenetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects.
- Is Sonic hedgehog (SHH) a candidate gene for spina bifida? A pilot study.
- Lack of association between ZIC2 and ZIC3 genes and the risk of neural tube defects (NTDs) in Hispanic populations.
- Apolipoprotein E and apolipoprotein B genotypes and risk for spina bifida.
- Maternal periconceptional vitamins: interactions with selected factors and congenital anomalies?
- Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.
- Genitopatellar syndrome: delineating the anomalies of female genitalia.
- Maternal periconceptional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida.
- Apolipoprotein B and apolipoprotein E genotypes and sporadic holoprosencephaly.
- The READIT assay as a method for genotyping NAT1*10 polymorphisms.
- Does prenatal screening for 5,10-methylenetetrahydrofolate reductase (MTHFR) mutations in high-risk neural tube defect pregnancies make sense?
Schools
University of Ia Roy J amp L Carver Com
University Ia College Med
Center Disease Control
Massachusetts General Hospital
Doctors Specialties
- Clinical Genetics
- Pediatrics
- Medical Genetics
Accepted Insurances
Awards
- Fellow (FAAP)
Education
-
University of Iowa Hospitals and Clinics -
University of Iowa Carver College of Medicine
Helpful Reviews
Similar Doctors
|
|
Dr. Gail P. Udkow, MD
 This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Bruce D. Blumberg, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Katherine G. Dawson, MD |
|
|
Dr. Michael E. Lang, MD |
|
|
Dr. Brian K. Linde, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Lawrence M. Ng, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Stuart Zangwill, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Kelley Meade, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Joan W. Roux, MD |
|
|
Dr. Erica B. Andrist, MD |
|
|
Dr. Omoniyi O. Omotoso, MD |
|
|
Dr. Leslie C. Manace, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Rashmi Jain, MD |
|
|
Dr. Elizabeth A. Trachtenberg, PHD |
|
|
Anna K. McGill
This Doctor is OpenDoctor Recommended.
|