S. Zneimer

发表

Regional assignment of two genes of the human branched-chain α-keto acid dehydrogenase complex: The E1β gene (BCKDHB) to chromosome 6p21–22 and the E2 gene (DBT) to chromosome 1p31

R. Eddy, T. Shows, D. Chuang, 1991 .

Regional assignment of two genes of the human branched-chain alpha-keto acid dehydrogenase complex: the E1 beta gene (BCKDHB) to chromosome 6p21-22 and the E2 gene (DBT) to chromosome 1p31.

R. Eddy, T. Shows, D. Chuang, 1991, Genomics.

Telomere‐telomere (end to end) fusion of chromosomes 7 and 22 with an interstitial deletion of chromosome 7p11.2→p15.1: phenotypic consequences and possible mechanisms

P. Cotter, S. Zneimer, P. Cotter, 2000, Clinical genetics.

Visible deletions, duplications and insertions

S. Zneimer, 2014 .

Results with constitutional or other non‐neoplastic abnormalities

S. Zneimer, 2014 .

Cytogenetic abnormalities in solid tumors

S. Zneimer, 2014 .

GUIDELINES FOR GOOD CLINICAL LABORATORY PRACTICE

S. Zneimer, 2016 .

Bladder cancer FISH analysis

S. Zneimer, 2014 .

Unidentifiable marker chromosomes, derivative chromosomes, chromosomes with additional material and rings

S. Zneimer, 2014 .

Quality Assurance of Non-Invasive Prenatal Screening (NIPS) for Fetal Aneuploidy Using Positive Predictive Values as Outcome Measures

Z. Demko, S. Zneimer, P. Benn, 2019, Journal of clinical medicine.

Non-Invasive Prenatal Screening of Over 200,000 Tests Performed at Natera

S. Zneimer, 2016 .

In situ hybridization shows direct evidence of skewed X inactivation in one of monozygotic twin females manifesting Duchenne muscular dystrophy.

C. Richards, N. Schneider, S. Zneimer, 1993, American journal of medical genetics.

Balanced translocation 12/13 and situs abnormalities: homology of early pattern formation in man and lower organisms?

Golder N Wilson, N. Schneider, L. Gilstrap, 1991, American journal of medical genetics.

Cytogenetic abnormalities in lymphoid disorders

S. Zneimer, 2014 .

Recurrent FISH abnormalities in lymphoid disorders

S. Zneimer, 2014 .

Partial trisomy of chromosome 6q: an interstitial duplication of the long arm.

R. Bachman, S. Zneimer, B. Ziel, 1998, American journal of medical genetics.

Deletion of the c-kit protooncogene in the human developmental defect piebald trait.

V. Stastny, D. Saltman, R. Fleischman, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Chromosomal microarrays for tumors

S. Zneimer, 2014 .

Bacterial artificial chromosome, oligoarray and single nucleotide polymorphism array methodologies for analysis

S. Zneimer, 2014 .

Microarray abnormal results

S. Zneimer, 2014 .

Pathogenic chromosomal microarray copy number changes by chromosome order

S. Zneimer, 2014 .

Fetal demises/spontaneous abortions

S. Zneimer, 2014 .

A novel sequencing-based vaginal health assay combining self-sampling, HPV detection and genotyping, STI detection, and vaginal microbiome analysis

Sara W. Bird, J. P. Cárdenas, N. A. Walton, 2019, PloS one.

Common biphenotypic abnormalities and secondary changes

S. Zneimer, 2014 .

Regional localization of the fibronectin and γ-crystallin genes to bovine chromosome 8

J. Womack, S. Zneimer, 1989 .

Self-Sampling for Human Papillomavirus Testing: Increased Cervical Cancer Screening Participation and Incorporation in International Screening Programs

Sara W. Bird, J. P. Cárdenas, N. A. Walton, 2018, Front. Public Health.

Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population

Z. Demko, A. Gropman, E. Kırkızlar, 2016, PloS one.

Reporting complex abnormalities and multiple cell lines

S. Zneimer, 2014 .

Components of a standard cytogenetics report, normal results and culture failures

S. Zneimer, 2014 .

Autosomal trisomies – prenatal and livebirths

S. Zneimer, 2014 .

Cytogenetic Abnormalities: Chromosomal, FISH, and Microarray-Based Clinical Reporting

S. Zneimer, 2014 .

D. Douer, Stephen V. Liu, S. Zneimer, 2011, Acta Haematologica.

Mapping of the human ribonuclease inhibitor gene (RNH) to chromosome 11p15 by in situ hybridization.

N. Schneider, S. Zneimer, D. Crawford, 1990, Genomics.

Recurrent FISH abnormalities in solid tumors using paraffin‐embedded tissue

S. Zneimer, 2014 .

Validation of Fluorescence In Situ Hybridization (FISH) for Chromosome 5 Monosomy and Deletion

S. Zneimer, 2020, Current protocols in human genetics.

Chromosomal microarray analysis for hematological disorders

S. Zneimer, 2014 .

Introduction to FISH analysis for hematological disorders and solid tumors

S. Zneimer, 2014 .

Sex chromosome abnormalities

S. Zneimer, 2014 .

Composite karyotypes and other complex rearrangements

S. Zneimer, 2014 .

REAGENTS, INSTRUMENTS, AND EQUIPMENT

Susan Mahler Zneimer, S. Zneimer, 2016 .