M. Blitzer

A. Baschat, M. Blitzer, J. Kopelman, 2010, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

The 2019 US medical genetics workforce: a focus on clinical genetics

M. Watson, H. Andersson, M. Muenke, 2021, Genetics in Medicine.

Asparaginase Erwinia chrysanthemi effectively depletes plasma glutamine in adult patients with relapsed/refractory acute myeloid leukemia

E. Sausville, L. Jeng, M. Blitzer, 2017, Cancer Chemotherapy and Pharmacology.

3-hydroxy-3-methylglutaryl-coenzyme a lyase deficiency: Report of five new patients

M. Blitzer, K. Gibson, J. Breuer, 1988, Journal of Inherited Metabolic Disease.

REPORT FROM THE ASHG INFORMATION AND EDUCATION COMMITTEE : MEDICAL SCHOOL CORE CURRICULUM IN GENETICS

R. Pagon, L. Elsas, M. Blitzer, 1995 .

Educational innovations in clinical pharmacogenomics

A. Shuldiner, A. Shuldiner, A. Beitelshees, 2016, Clinical pharmacology and therapeutics.

Development and characterization of a mouse with profound biotinidase deficiency: a biotin-responsive neurocutaneous disorder.

Caiying Guo, M. Blitzer, K. Pindolia, 2011, Molecular genetics and metabolism.

Technical standards and guidelines for the diagnosis of biotinidase deficiency

T. Cowan, M. Blitzer, B. Wolf, 2010, Genetics in Medicine.

Biotinidase deficiency: Novel mutations and their biochemical and clinical correlates

D. Goudie, M. Blitzer, Helio F. Pedro, 2005, Human mutation.

Partial biotinidase deficiency: clinical and biochemical features.

M. Blitzer, B. Wolf, H. Levy, 1990, The Journal of pediatrics.

Evidence for an intracerebral action of phenylalanine in stimulation of prolactin secretion: interaction of large neutral amino acids.

M. Blitzer, D. Hyman, H. Carlson, 1990, The Journal of clinical endocrinology and metabolism.

Relationship between first-trimester serum placental protein-13 and maternal characteristics, placental Doppler studies and pregnancy outcome

A. Baschat, M. Blitzer, H. Meiri, 2016, Journal of perinatal medicine.

Medical genetics and genomics training in obstetrics and gynecology residencies: are we ready for the future?

R. Sokol, M. Blitzer, G. Feldman, 2019, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Profound biotinidase deficiency in two asymptomatic adults.

M. Blitzer, D. Mock, B. Wolf, 1997, American journal of medical genetics.

Partial biotinidase deficiency' and biochemical features Clinical

M. Blitzer, B. Wolf, H. Levy, 1990 .

Transient neonatal galactosaemia identified by newborn screening

L. Raffel, T. Cowan, M. Blitzer, 1993, Journal of Inherited Metabolic Disease.

Prediction of preeclampsia utilizing the first trimester screening examination.

L. Magder, A. Baschat, M. Blitzer, 2014, American Journal of Obstetrics and Gynecology.

Second‐trimester maternal serum analyte levels associated with fetal trisomy 13

J. Canick, J. Haddow, G. Palomaki, 1999, Prenatal diagnosis.

Multiple-marker screening in pregnancies with hydropic and nonhydropic Turner syndrome.

J. Canick, M. Blitzer, D. Saller, 1992, American journal of obstetrics and gynecology.

Antenatal detection of cystic hygroma.

S. Schwartz, L. Raffel, K. Blakemore, 1989, Obstetrical & gynecological survey.

The "muscular variant" of Pompe disease: clinical, biochemical and histologic characteristics.

M. Blitzer, D. Dunn, E. Shapira, 1985, American journal of medical genetics.

Next-generation DNA sequencing of HEXA: a step in the right direction for carrier screening

G. Porreca, J. Hoffman, B. Bishop, 2013, Molecular genetics & genomic medicine.

Intrafamilial variability in Hurler syndrome and Sanfilippo syndrome type A: implications for evaluation of new therapies.

T. Cowan, M. Blitzer, C. Greene, 1993, American journal of medical genetics.

Recommendations of core competencies in genetics essential for all health professionals

A. Patenaude, A. Guttmacher, M. Blitzer, 2001, Genetics in Medicine.

The state of the medical geneticist workforce: Findings of the 2003 survey of American Board of Medical Genetics certified geneticists

J. Benkendorf, M. Blitzer, G. Forte, 2005, Genetics in Medicine.

Erythrocyte uridine diphosphate galactose-4- epimerase deficiency identified by newborn screening for galactosemia in the United States

T. Cowan, H. Bock, M. Blitzer, 1993 .

A Purified Serum Glycopeptide from Controls and Cystic Fibrosis Patients. I. Comparison of their Mucociliary Activity on Rabbit Tracheal Explants

M. Blitzer, E. Shapira, 1982, Pediatric Research.

Evaluation of inorganic pyrophosphate in amniotic fluid as a mode of prenatal diagnosis of osteogenesis imperfecta

M. Blitzer, K. Garver, S. Marchese, 1984, Prenatal diagnosis.

Maroteaux-Lamy syndrome in a large consanguineous kindred: biochemical and immunological studies.

M. Blitzer, S. Black, J. Miller, 1986, American journal of medical genetics.

Marinesco‐Sjögren syndrome

M. Blitzer, E. Shapira, P. Walker, 1985, Neurology.

U.S. genetics nurses in advanced practice.

Janet K. Williams, M. Blitzer, P. A. Flanagan, 2006, Journal of nursing scholarship : an official publication of Sigma Theta Tau International Honor Society of Nursing.

First-trimester angiopoietin-2: relationships with maternal and placental characteristics.

A. Baschat, M. Blitzer, C. Harman, 2010, American journal of perinatology.

First-trimester prediction of small-for-gestational age neonates incorporating fetal Doppler parameters and maternal characteristics.

A. Baschat, M. Blitzer, J. Kopelman, 2014, American journal of obstetrics and gynecology.

Maternal blood‐pressure trends throughout pregnancy and development of pre‐eclampsia in women receiving first‐trimester aspirin prophylaxis

A. Baschat, M. Blitzer, V. Seravalli, 2018, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

The training of future clinical geneticists: Evaluation and reflection on the American College of Medical Genetics and Genomics Foundation Summer Genetics Scholars Program

M. Blitzer, S. Klugman, Carly E. Blatt, 2021, Genetics in Medicine.

Discrimination of phenylketonurics from persistent hyperphenylalaninemia patients using a simple phenylalanine loading test.

M. Blitzer, E. Shapira, J. E. Bailey-Wilson, 1985, Clinica chimica acta; international journal of clinical chemistry.

Discrimination of heterozygotes for phenylketonuria, persistent hyperphenylalaninemia and controls by phenylalanine loading.

M. Blitzer, E. Shapira, J. E. Bailey-Wilson, 1986, Clinica chimica acta; international journal of clinical chemistry.

The medical genetics workforce: An analysis of clinical geneticist subgroups

J. Benkendorf, M. Blitzer, P. A. Flanagan, 2006, Genetics in Medicine.

A Purified Serum Glycopeptide from Controls and Cystic Fibrosis Patients. II. Comparison of their Immunologic Properties Using Monoclonal Antibodies

M. Blitzer, E. Shapira, 1982, Pediatric Research.

Maternal blood pressures during pregnancy and the risk of delivering a small-for-gestational-age neonate

A. Baschat, M. Blitzer, D. Block-Abraham, 2016, Hypertension in pregnancy.

First-Trimester Risk Factors for Preeclampsia Development in Women Initiating Aspirin by 16 Weeks of Gestation

A. Baschat, M. Blitzer, J. Kopelman, 2014, Obstetrics and gynecology.

Implementation of pharmacogenetics: The University of Maryland personalized anti‐platelet pharmacogenetics program

Casey Lynnette Overby, Kristin A. Maloney, Mark D Kelemen, 2014, American journal of medical genetics. Part C, Seminars in medical genetics.

The presence of two different infantile Tay-Sachs disease mutations in a Cajun population.

M. Blitzer, E. Shapira, E. Mules, 1992, American journal of human genetics.

Second‐trimester maternal serum analyte levels associated with fetal trisomy 13

J. Canick, J. Haddow, G. Palomaki, 1999, Prenatal diagnosis.

A Purified Serum Glycopeptide from Controls and Cystic Fibrosis Patients. III. The Association of the Ciliary Dyskinetic Activity with the Oligosaccharide Component

M. Blitzer, E. Shapira, 1984, Pediatric Research.

External validity of first‐trimester algorithms in the prediction of pre‐eclampsia disease severity

A. Baschat, M. Blitzer, Lauren E. Doyle, 2014, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

First‐trimester prediction of pre‐eclampsia: external validity of algorithms in a prospectively enrolled cohort

A. Baschat, M. Blitzer, M. Blitzer, 2014, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.