C. Strom

C. Strom, N. Ginsberg, A. Cadkin, 1997, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Tay-Sachs carrier screening in the genomics age: Gene sequencing versus enzyme analysis in non-Jewish individuals

N. Park, C. Strom, B. Crossley, 2013 .

Qualitative assessment of FMR1 (CGG)n triplet repeat status in normal, intermediate, premutation, full mutation, and mosaic carriers in both sexes: Implications for fragile X syndrome carrier and newborn screening

Weimin Sun, C. Strom, F. Hantash, 2010, Genetics in Medicine.

Intrapartum management relating to the risk of perinatal transmission of group B streptococcus.

C. Strom, E. Levine, J. Barton, 1998, Infectious diseases in obstetrics and gynecology.

Preimplantation diagnosis for ornithine transcarbamylase deficiency.

C. Strom, S. Rechitsky, O. Verlinsky, 2000, Reproductive biomedicine online.

Improving the Accuracy of Prenatal Screening with DNA Copy-Number Analysis.

C. Strom, R. Owen, Megan D. Maxwell, 2017, The New England journal of medicine.

Development of a novel, accurate, automated, rapid, high-throughput technique suitable for population-based carrier screening for Fragile X syndrome

Weimin Sun, C. Strom, F. Hantash, 2007, Genetics in Medicine.

Reliability of gender determination using the polymerase chain reaction (PCR) for single cells

C. Strom, S. Rechitsky, Y. Verlinsky, 1991, Journal of in Vitro Fertilization and Embryo Transfer.

Three births after preimplantation genetic diagnosis for cystic fibrosis with sequential first and second polar body analysis.

C. Strom, S. Rechitsky, A. Kuliev, 1998, American journal of obstetrics and gynecology.

Dna Analysis of Gametes and Embryos: Analysis of Delta-F508 Cystic Fibrosis Mutation in Single Cells

C. Strom, S. Rechitsky, G. Enriquez, 1991 .

Preimplantation Genetic Analysis Using PCR

C. Strom, S. Rechitsky, G. Enriquez, 1991 .

Preconception genetic diagnosis of cystic fibrosis

C. Strom, N. Ginsberg, Y. Verlinsky, 1990, The Lancet.

Sequence variations in AGTR2 are unlikely to be associated with X‐linked mental retardation

Weimin Sun, C. Strom, Donghui Huang, 2005, American journal of medical genetics. Part A.

The dangers of including nonclassical cystic fibrosis variants in population-based screening panels: p.L997F, further genotype/phenotype correlation data

C. Strom, Mei Peng, J. Redman, 2011, Genetics in Medicine.

Discordant noninvasive prenatal testing and cytogenetic results: a study of 109 consecutive cases

C. Strom, Jia-Chi Wang, Leslie P Ross, 2014, Genetics in Medicine.

Apparent homozygosity of a novel frame shift mutation in the CFTR gene because of a large deletion.

Weimin Sun, C. Strom, F. Hantash, 2009, The Journal of molecular diagnostics : JMD.

Polar body-based preimplantation diagnosis for X-linked disorders.

C. Strom, S. Rechitsky, O. Verlinsky, 2002, Reproductive biomedicine online.

Use of nested PCR to identify charred human remains and minute amounts of blood.

C. Strom, S. Rechitsky, 1998, Journal of forensic sciences.

Chromosomal abnormalities in the first and second polar body

C. Strom, A. Kuliev, Y. Verlinsky, 2001, Molecular and Cellular Endocrinology.

Reliability of preimplantation diagnosis for single gene disorders

C. Strom, S. Rechitsky, O. Verlinsky, 2001, Molecular and Cellular Endocrinology.

PGDIS Position Statement on the Transfer of Mosaic Embryos 2019.

C. Rubio, S. Kahraman, C. Strom, 2019, Reproductive biomedicine online.

Designer babies - are they a reality yet? Case report: simultaneous preimplantation genetic diagnosis for Fanconi anaemia and HLA typing for cord blood transplantation.

C. Strom, S. Rechitsky, A. Kuliev, 2000, Reproductive biomedicine online.

Preimplantation diagnosis for Fanconi anemia combined with HLA matching.

C. Strom, S. Rechitsky, A. Kuliev, 2001, JAMA.

CHRONIC VAGINAL CANDIDIASIS RESPONSIVE TO BIOTIN THERAPY IN A CARRIER OF BIOTINIDASE DEFICIENCY

C. Strom, E. Levine, 1998, Obstetrics and gynecology.

Characterization of a complex chromosomal rearrangement using chromosome, FISH, and microarray assays in a girl with multiple congenital abnormalities and developmental delay

C. Strom, Jia-Chi Wang, F. Boyar, 2014, Molecular Cytogenetics.

Invasive trophoblast antigen (hyperglycosylated human chorionic gonadotropin) in second-trimester maternal urine as a marker for down syndrome: preliminary results of an observational study on fresh samples.

G. Knight, G. Palomaki, C. Strom, 2004, Clinical chemistry.

The sensitivity and specificity of hyperglycosylated hCG (hhCG) levels to reliably diagnose clinical IVF pregnancies at 6 days following embryo transfer

C. Strom, R. Alvero, M. Cedars, 2012, Journal of Assisted Reproduction and Genetics.

Current and Future Perspectives of Fetal Genetic Diagnosis

C. Strom, E. Pergament, B. Fine, 1990 .

Prenatal diagnosis of 46,XX male fetuses.

C. Strom, N. Ginsberg, Y. Verlinsky, 1999, American journal of obstetrics and gynecology.

Isolation of cDNA libraries from individual human preimplantation embryos.

C. Strom, S. Rechitsky, O. Verlinsky, 1998, Molecular human reproduction.

Distribution of 5-bromodeoxyuridine and thymidine in the DNA of developing chick cartilage.

C. Strom, A. Dorfman, 1976, Proceedings of the National Academy of Sciences of the United States of America.

Isolation and characterization of genomic clones corresponding to the human type II procollagen gene.

C. Strom, W. B. Upholt, 1984, Nucleic acids research.

Allele Dropout in Polar Bodies and Blastomeres

C. Strom, S. Rechitsky, O. Verlinsky, 1998, Journal of Assisted Reproduction and Genetics.

Preembryonic diagnosis for sickle cell disease

C. Strom, S. Rechitsky, O. Verlinsky, 2001, Molecular and Cellular Endocrinology.

Short stature, digit anomalies and dysmorphic facial features are associated with the duplication of miR-17 ~ 92 cluster

C. Strom, F. Boyar, A. Anguiano, 2014, Molecular Cytogenetics.

A Standardized DNA Variant Scoring System for Pathogenicity Assessments in Mendelian Disorders

Glenn A. Maston, Weimin Sun, C. Strom, 2015, Human mutation.

6 and Future Perspectives of Fetal Genetic Diagnosis

C. Strom, E. Pergament, B. Fine, 1990 .

Frequency and Complexity of De Novo Structural Mutation in Autism.

Amina Noor, Kang Zhang, Dheeraj Malhotra, 2016, American journal of human genetics.

Multiple Property Tolerance Analysis for the Evaluation of Missense Mutations

Tai-Sung Lee, Steven J. Potts, Matthew J. McGinniss, 2006, Evolutionary bioinformatics online.

Birth of healthy children after preimplantation diagnosis of common aneuploidies by polar body fluorescent in situ hybridization analysis. Preimplantation Genetics Group.

C. Strom, A. Kuliev, Y Verlinsky, 1996, Fertility and sterility.

Inherited and de novo 22q11.2 distal duplications in two patients with autistic features, speech delay and no dysmorphology

C. Strom, F. Hantash, R. Owen, 2012, Journal of Pediatric Genetics.

Prenatal paternity testing with deoxyribonucleic acid techniques.

C. Strom, S. Rechitsky, O. Verlinsky, 1996, American journal of obstetrics and gynecology.

Allele dropout in sequential PCR and FISH analysis of single cells (cell recycling)

C. Strom, S. Rechitsky, Y. Verlinsky, 1996, Journal of Assisted Reproduction and Genetics.

Birth of Healthy Children After Preimplantation Diagnosis of Thalassemias

C. Strom, S. Rechitsky, O. Verlinsky, 1999, Journal of Assisted Reproduction and Genetics.

Preimplantation Diagnosis of Thalassemias

C. Strom, S. Rechitsky, O. Verlinsky, 1998, Journal of Assisted Reproduction and Genetics.

Genotype-phenotype correlation and frequency of the 3199del6 cystic fibrosis mutation among I148T carriers: Results from a collaborative study

Weimin Sun, C. Strom, M. Friez, 2004, Genetics in Medicine.

Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing.

Matthew Rabinowitz, Allison Ryan, Milena Banjevic, 2014, American journal of obstetrics and gynecology.

Clinical array comparative genomic hybridization: a new paradigm.

C. Strom, R. Owen, A. Anguiano, 2008, Expert opinion on medical diagnostics.

Spectral Karyotyping for identification of constitutional chromosomal abnormalities at a national reference laboratory

Charles M Strom, Vladimira Sulcova, C. Strom, 2012, Molecular Cytogenetics.

Analyses of 95 first-trimester spontaneous abortions by chorionic villus sampling and karyotype

C. Strom, N. Ginsberg, Y. Verlinsky, 1992, Journal of Assisted Reproduction and Genetics.

Analysis of the first polar body: preconception genetic diagnosis.

C. Strom, Y Verlinsky, A Lifchez, 1990, Human reproduction.

Current status of preimplantation diagnosis

C. Strom, K. Sermon, A. Kuliev, 1997, Journal of Assisted Reproduction and Genetics.

Preconception and preimplantation diagnosis for cystic fibrosis

C. Strom, S. Rechitsky, Y. Verlinsky, 1992, Prenatal diagnosis.

Obstetric outcomes in 102 pregnancies after preimplantation genetic diagnosis.

C. Strom, E. Levine, N. Ginsberg, 2000, American journal of obstetrics and gynecology.

Prepregnancy genetic testing for age-related aneuploidies by polar body analysis.

C. Strom, A. Kuliev, N. Ginsberg, 1997, Genetic testing.

Pediatrician attendance at cesarean delivery: necessary or not?

C. Strom, E. Levine, J. Barton, 1999, Obstetrics and gynecology.

FMR1 premutation carrier frequency in patients undergoing routine population-based carrier screening: Insights into the prevalence of fragile X syndrome, fragile X-associated tremor/ataxia syndrome, and fragile X-associated primary ovarian insufficiency in the United States

Weimin Sun, C. Strom, F. Hantash, 2011, Genetics in Medicine.

Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel

Victoria M. Pratt, Michael S. Watson, Wayne W. Grody, 2004, Genetics in Medicine.

Short stature, digit anomalies and dysmorphic facial features are associated with the duplication of miR-17 ~ 92 cluster

C. Strom, F. Boyar, A. Anguiano, 2014, Molecular Cytogenetics.

A Multigene Test Could Cost-Effectively Help Extend Life Expectancy for Women at Risk of Hereditary Breast Cancer.

Charles M Strom, C. Strom, R. Bender, 2017, Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research.

Analysis of three restriction fragment length polymorphisms in the human type II procollagen gene.

C. Strom, C. E. Eng, 1985, American journal of human genetics.

Chapter 13 – Thrombophilia

C. Strom, M. Sahud, Charles Strom, 2010 .

BRCA Share: A Collection of Clinical BRCA Gene Variants

Christophe Béroud, Dominique Vaur, Izabela Karbassi, 2016, Human mutation.

Submicroscopic deletion of 5q involving tumor suppressor genes (CTNNA1, HSPA9) and copy neutral loss of heterozygosity associated with TET2 and EZH2 mutations in a case of MDS with normal chromosome and FISH results

C. Strom, F. Boyar, A. Anguiano, 2014, Molecular Cytogenetics.

Preimplantation diagnosis for p53 tumour suppressor gene mutations.

Z. Rosenwaks, C. Strom, S. Rechitsky, 2001, Reproductive biomedicine online.

Current progress in preimplantation genetic diagnosis

C. Readhead, C. Strom, P. Sutter, 1993, Journal of Assisted Reproduction and Genetics.

Preimplantation Diagnosis of Common Aneuploidies by the First- and Second-Polar Body FISH Analysis

C. Strom, A. Kuliev, N. Ginsberg, 1998, Journal of Assisted Reproduction and Genetics.

Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes

Colin A. Johnson, K. Cibulskis, S. Gabriel, 2010, Nature Genetics.

Molecular testing for Fragile X Syndrome: Lessons learned from 119,232 tests performed in a clinical laboratory

Weimin Sun, C. Strom, Mei Peng, 2007, Genetics in Medicine.

Prevalence of known mutations in the familial Mediterranean fever gene (MEFV) in various carrier screening populations

Weimin Sun, C. Strom, M. Mikula, 2008, Genetics in Medicine.

Cross‐hybridization of the chromosome 13/21 alpha satellite DNA probe to chromosome 22 in the prenatal screening of common chromosomal aneuploidies by fish

C. Strom, A. Kuliev, N. Ginsberg, 1995, Prenatal diagnosis.

Molecular combing compared to Southern blot for measuring D4Z4 contractions in FSHD

Y. Liu, Weimin Sun, C. Strom, 2015, Neuromuscular Disorders.

Preimplantation diagnosis of single gene disorders by two-step oocyte genetic analysis using first and second polar body.

C. Strom, S. Rechitsky, A. Kuliev, 1997, Biochemical and molecular medicine.

Reliability of polymerase chain reaction (PCR) analysis of single cells for preimplantation genetic diagnosis

C. Strom, S. Rechitsky, Y. Verlinsky, 1994, Journal of Assisted Reproduction and Genetics.

Homeobox gene expression in human oocytes and preembryos

C. Strom, S. Rechitsky, O. Verlinsky, 1995, Molecular reproduction and development.

Preimplantation diagnosis of autosomal dominant retinitis pigmentosum using two simultaneous single cell assays for a point mutation in the rhodopsin gene.

C. Strom, S. Rechitsky, A. Kuliev, 1998, Molecular human reproduction.

High-throughput gene sequencing assay development for hereditary nonpolyposis colon cancer.

Weimin Sun, C. Strom, R. Bender, 2004, Clinical colorectal cancer.

Polar body diagnosis of common aneuploidies by FISH

C. Strom, A. Kuliev, N. Ginsberg, 1996, Journal of Assisted Reproduction and Genetics.

Decreasing risk of pregnancy loss following chorionic villus sampling. Elimination of transabdominal chorionic villus sampling during the ninth week of pregnancy.

C. Strom, N. Ginsberg, Y. Verlinsky, 1992, Journal of reproductive medicine.

Genetically characterized positive control cell lines derived from residual clinical blood samples.

S. Thibodeau, D. H. Farkas, C. Strom, 2005, Clinical chemistry.

Extensive sequencing of the cystic fibrosis transmembrane regulator gene: Assay validation and unexpected benefits of developing a comprehensive test

Weimin Sun, C. Strom, Mei Peng, 2003, Genetics in Medicine.

Term birth after midtrimester hysterotomy and selective delivery of an acardiac twin.

C. Strom, S. Rabin, N. Ginsberg, 1992, American journal of obstetrics and gynecology.

Preimplantation diagnosis for long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

C. Strom, S. Rechitsky, O. Verlinsky, 2001, Reproductive biomedicine online.

Prepregnancy testing for single-gene disorders by polar body analysis.

C. Strom, S. Rechitsky, O. Verlinsky, 1999, Genetic testing.

Construction and Sequence Analysis of Subtraction Complementary DNA Libraries from Human Preimplantation Embryos

C. Strom, S. Rechitsky, O. Verlinsky, 1999, Journal of Assisted Reproduction and Genetics.

Molecular studies in achondroplasia using Co12A1 probes.

C. Strom, 1988, Basic life sciences.

863 DETECTION OF GENE DELETIONS IN THE HUMAN TYPE II PROCOLLAGEN GENE IN 8 PATIENTS WITH ACHONDROPLASIA USING GENE DOSAGE ANALYSIS

C. Strom, R. Pauli, T. Christides, 1985, Pediatric Research.

ACHONDROPLASIA DUE TO DNA INSERTION INTO THE TYPE II COLLAGEN GENE

C. Strom, 1984, Pediatric Research.

Amplification of moderately repetitive DNA sequences during chick cartilage differentiation.

C. Strom, A. Dorfman, 1976, Proceedings of the National Academy of Sciences of the United States of America.

Double-blind, placebo-controlled crossover study of folinic acid (Leucovorin for the treatment of fragile X syndrome.

C. Strom, W. Pizzi, R. Brusca, 1992, American journal of medical genetics.

Detection of 677CT/1298AC “double variant” chromosomes: Implications for interpretation of MTHFR genotyping results

Weimin Sun, C. Strom, M. Mcginniss, 2005, Genetics in Medicine.

Direct visualization of cystic fibrosis transmembrane regulator mutations in the clinical laboratory setting.

David D. Clark, Weimin Sun, Charles M Strom, 2004, Clinical chemistry.

A large deletion in the CFTR gene in CBAVD

Weimin Sun, C. Strom, F. Hantash, 2006, Genetics in Medicine.

Current challenges in cystic fibrosis screening.

C. Strom, 2004, Archives of pathology & laboratory medicine.

Characterization of a recurrent novel large duplication in the cystic fibrosis transmembrane conductance regulator gene.

Weimin Sun, C. Strom, F. Hantash, 2007, The Journal of molecular diagnostics : JMD.

Preimplantation diagnosis of genetic and chromosomal disorders

C. Readhead, N. Arnheim, C. Strom, 1994, Journal of Assisted Reproduction and Genetics.

Expression of homeobox-containing genes in human preimplantation development and in embryos with chromosomal aneuploidies

C. Strom, S. Rechitsky, O. Verlinsky, 1996, Journal of Assisted Reproduction and Genetics.

The importance of β globin deletion analysis in the evaluation of patients with β thalassemia

C. Strom, M. Gallivan, M. Mikula, 2011, International journal of laboratory hematology.

Rapid one-step carrier detection assay of mucolipidosis IV mutations in the Ashkenazi Jewish population.

Weimin Sun, C. Strom, F. Hantash, 2006, The Journal of molecular diagnostics : JMD.

Detection of translocations involving the Y‐chromosome in prospective prenatal screening of common chromosomal aneuploidies by FISH

C. Strom, A. Kuliev, N. Ginsberg, 1998, Prenatal Diagnosis.

Preimplantation testing for phenylketonuria.

C. Strom, S. Rechitsky, O. Verlinsky, 2001, Fertility and Sterility.

Novel and recurrent rearrangements in the CFTR gene: clinical and laboratory implications for cystic fibrosis screening

Weimin Sun, C. Strom, F. Hantash, 2006, Human Genetics.

High Frequency of Meiosis II Aneuploidies in IVF Patients of Advanced Maternal Age

C. Strom, A. Kuliev, Y. Verlinsky, 2000 .

Consultations in Molecular Diagnostics Characterization of a Recurrent Novel Large Duplication in the Cystic Fibrosis Transmembrane Conductance Regulator Gene

Weimin Sun, C. Strom, F. Hantash, 2007 .

Improving the Positive Predictive Value of Non-Invasive Prenatal Screening (NIPS)

J. Catanese, Weimin Sun, C. Strom, 2017, PloS one.

Technical validation of a multiplex platform to detect thirty mutations in eight genetic diseases prevalent in individuals of Ashkenazi Jewish descent

Arlene Buller, Franklin Quan, Weimin Sun, 2005, Genetics in Medicine.