W. Kearns

发表

Maternal XX/X chromosome mosaicism in donor oocyte in vitro fertilization (IVF)

M. Christianson, P. Brezina, K.-H. D. Nguyen, 2012 .

The isolation of cDNAs from OATL1 at Xp 11.2 using a 480-kb YAC.

A. Monaco, D. Valle, H. Lehrach, 1993, Genomics.

Erratum: Introduction and expression of the 400 kilobase amyloid precursor protein gene in transgenic mice (Nature Genetics (1993) 5 (22-30))

D. Price, C. Kitt, J. Gearhart, 1993 .

Introduction and expression of the 400 kilobase amyloid precursor protein gene in transgenic mice [corrected].

D. Price, C. Kitt, J. Gearhart, 1993, Nature genetics.

Reprogramming within hours following nuclear transfer into mouse but not human zygotes.

Alice E. Chen, D. Melton, K. Eggan, 2011, Nature communications.

Embryo quality, ploidy, and transfer outcomes in male versus female blastocysts

W. Kearns, J. Crochet, Antonio F. Saad, 2021, Journal of Assisted Reproduction and Genetics.

Detection of aneuploidy for chromosomes 4, 6, 7, 8, 9, 10, 11, 12, 13, 17, 18, 21, X and Y by fluorescence in-situ hybridization in spermatozoa from nine patients with oligoasthenoteratozoospermia undergoing intracytoplasmic sperm injection.

A. Cuticchia, G. Doncel, M. Pang, 1999, Human reproduction.

Reproductive ovarian testing and the alphabet soup of diagnoses: DOR, POI, POF, POR, and FOR

J. Segars, M. Christianson, W. Kearns, 2017, Journal of Assisted Reproduction and Genetics.

Antenatal antioxidants to avert autism?

A. Quaas, W. Kearns, 2020, Journal of Assisted Reproduction and Genetics.

Cost-effectiveness of preimplantation genetic testing for aneuploidy for fresh donor oocyte cycles

M. Christianson, V. Baker, W. Kearns, 2020, F&S reports.

Increased risk for aplastic anemia and myelodysplastic syndrome in individuals lacking glutathione S‐transferase genes

N. Young, Johnson M Liu, M. Stacey, 2004, Pediatric blood & cancer.

ESHRE PGD Consortium data collection V: cycles from January to December 2002 with pregnancy follow-up to October 2003.

N. Muntjewerff, K. Vesela, C. Moutou, 2008, Human reproduction.

Nuclear receptor co‐repressor gene localizes to 17p11.2, a frequently deleted band in malignant disorders

Jianxiang Wang, Johnson M Liu, M. Stacey, 1999, Genes, chromosomes & cancer.

Assignment of the hypoxia-inducible factor 1alpha gene to a region of conserved synteny on mouse chromosome 12 and human chromosome 14q.

G. Semenza, N. Iyer, M. Pang, 1996, Genomics.

Lack of site-specific integration of the recombinant adeno-associated virus 2 genomes in human cells.

S. Ponnazhagan, A. Srivastava, A. Srivastava, 1997, Human gene therapy.

Recombinant adeno-associated virus (AAV-CFTR) vectors do not integrate in a site-specific fashion in an immortalized epithelial cell line.

T. Flotte, M. Landrum, G. Cutting, 1996, Gene therapy.

In vivo model of adeno-associated virus vector persistence and rescue

T. Flotte, T. Reynolds, G. Cutting, 1996, Journal of virology.

Comparative cytogenetic analysis between cyclophosphamide‐sensitive and ‐resistant lines of acute myeloid leukemia in the lewis brown norway hybrid rat

W. Kearns, A. Yeager, Todd Koelling, 1990, Genes, chromosomes & cancer.

Genomic instability in bone marrow failure syndromes

N. Young, J. Maciejewski, Johnson M Liu, 2004, American journal of hematology.

Centrosome amplification and aneuploidy in bone marrow failure patients

N. Young, Johnson M Liu, W. Kearns, 2004, Genes, chromosomes & cancer.

Preimplantation Genetic Diagnosis and Screening

W. Kearns, K. Richter, J. Graham, 2005, Seminars in reproductive medicine.

Preimplantation genetic testing for aneuploidy: what technology should you use and what are the differences?

P. Brezina, W. Kearns, R. Anchan, 2016, Journal of Assisted Reproduction and Genetics.

The current status of preimplantation genetic screening

W. Kearns, 2010 .

Physical mapping of the nail patella syndrome interval at 9q34: ordering of STSs and ESTs

M. K. McCormick, K. Scott, J. Richards, 1998, Human Genetics.

Aneuploidy frequencies in semen fractions from ten oligoasthenoteratozoospermic patients donating sperm for intracytoplasmic sperm injection.

M. Pang, M. Stacey, S. Oehninger, 1999, Fertility and sterility.

Severe hemophilia A in a female by cryptic translocation: order and orientation of factor VIII within Xq28.

B. Migeon, J. Axelman, S. Antonarakis, 1993, Genomics.

Preimplantation Genetic Testing

P. Brezina, W. Kearns, Michael A. Kutteh, 2013, Current Obstetrics and Gynecology Reports.

Does theFMR1 gene affect IVF success?

M. Christianson, Bailey McGuinness, W. Kearns, 2019, Reproductive biomedicine online.

Cellular and genetic analysis of oocytes and embryos in a human case of spontaneous oocyte activation.

C. Racowsky, C. Combelles, W. Kearns, 2011, Human reproduction.

The evolving role of genetics in reproductive medicine.

P. Brezina, W. Kearns, 2014, Obstetrics and gynecology clinics of North America.

Preimplantation Genetic Testing: Available and Emerging Technologies

G. Schattman, R. Elias, P. Brezina, 2012 .

Two different microarray technologies for preimplantation genetic diagnosis and screening, due to reciprocal translocation imbalances, demonstrate equivalent euploidy and clinical pregnancy rates

P. Brezina, A. Benner, W. Kearns, 2014, Journal of Assisted Reproduction and Genetics.

Detection by Fluorescence In-Situ Hybridization of Chromosome-4, Chromosome-6, Chromosome-7, Chromosome-8, Chromosome-9, Chromosome-10, Chromosome-11, Chromosome-12, Chromosome-13, Chromosome-17, Chromosome-18, Chromosome-21, Chromosome-X and Chromosome-y Aneuploidy in Sperm from Oligo-Astheno-Terat

A. Cuticchia, M. Pang, W. Kearns, 1994 .

Molecular cytogenetic analysis of sperm from infertile males undergoing intracytoplasmic sperm injection.

D. Griffin, G. Doncel, M. Pang, 2000, Methods in molecular biology.

Cytogenetics of somatic cells and sperm from a 46,XY/45,X mosaic male with moderate oligoasthenoteratozoospermia.

G. Doncel, M. Pang, W. Kearns, 1998, Fertility and sterility.

Introduction and expression of the 400 kilobase precursor amyloid protein gene in transgenic mice

D. Price, C. Kitt, J. Gearhart, 1993, Nature Genetics.

Origin of chromosome rearrangements in two long-lived human keratinocyte lines

P. Pearson, G. Stetten, J. Littlefield, 1991, In Vitro Cellular & Developmental Biology - Animal.

A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridization

P. Pearson, D. Batista, G. Stetten, 1993, Human Genetics.

Duplication of the short arm of the X chromosome in mother and daugther

D. Batista, W. Kearns, W. Wertelecki, 1993, Human Genetics.

Unbalanced translocation, t(18;21), detected by fluorescence in situ hybridization (FISH) in a child with 18q- syndrome and a ring chromosome 21.

S. Antonarakis, P. Pearson, G. Stetten, 1993, American journal of medical genetics.

Analysis of reciprocal translocations by chromosome painting: applications and limitations of the technique.

P. Pearson, K. Blakemore, G. Stetten, 1992, American journal of human genetics.

Navigating the body of literature assessing BRCA1/2 mutations and markers of ovarian function: a systematic review and meta-analysis

J. Segars, M. Christianson, Bailey McGuinness, 2020, Journal of Assisted Reproduction and Genetics.

Embryonal mitochondrial DNA: relationship to embryo quality and transfer outcomes

W. Kearns, J. Crochet, A. Klimczak, 2018, Journal of Assisted Reproduction and Genetics.

Efficient Differentiation of Steroidogenic and Germ-Like Cells from Epigenetically-Related iPSCs Derived from Ovarian Granulosa Cells

T. Tuschl, Adam Kiezun, R. Maas, 2015, PloS one.

In vitro propagation of XXY human Klinefelter spermatogonial stem cells: A step towards new fertility opportunities

A. Atala, R. Swerdloff, M. Pettenati, 2022, Frontiers in Endocrinology.

Increased IVF pregnancy rates after microarray preimplantation genetic diagnosis due to parental translocations

Ying-pu Sun, Haixia Jin, P. Brezina, 2014, Systems biology in reproductive medicine.

Genetic normalization of differentiating aneuploid cleavage stage embryos

P. Brezina, W. Kearns, R. Anchan, 2013 .

Evaluation of 571 In Vitro Fertilization (IVF) Cycels and 4,873 Embryos Using 23-Chromosome Single Nucleotide Polymorphism (SNP) Microarray Preimplantation Genetic Screening (PGS)

P. Brezina, A. Benner, W. Kearns, 2012 .

The rate of de novo and inherited aneuploidy as determined by 23-chromosome single nucleotide polymorphism microarray (SNP) in embryos generated from parents with known chromosomal translocations

P. Brezina, A. Benner, W. Kearns, 2011 .

Blastocoel fluid from differentiated blastocysts harbors embryonic genomic material capable of a whole-genome deoxyribonucleic acid amplification and comprehensive chromosome microarray analysis.

Yulian Zhao, P. Brezina, A. Benner, 2015, Fertility and sterility.

The Incidence of Aneuploidy Significantly Increases After the Age of 40 in Women With a History of Recurrent Pregnancy Loss

A. Benner, W. Kearns, K. Tobler, 2012 .

Absence of donor-derived keratinocyte stem cells in skin tissues cultured from patients after mobilized peripheral blood hematopoietic stem cell transplantation.

R. Childs, C. Dunbar, E. Sloand, 2002, Experimental hematology.

Expression of the human multidrug resistance and glucocerebrosidase cDNAs from adeno-associated vectors: efficient promoter activity of AAV sequences and in vivo delivery via liposomes.

T. Flotte, I. Pastan, M. Gottesman, 1996, Human gene therapy.

Detection of chromosomal aberrations in interphase and metaphase cells in prenatal and postnatal studies.

P. Pearson, W. Kearns, 1994, Methods in molecular biology.

Genetic Normalization of Differentiating Aneuploid Human Embryos

G. Cutting, K.-H. D. Nguyen, A. Benner, 2011 .

A 2019 reproductive update from the Midwest Reproductive Symposium International

J. Zolton, W. Kearns, A. Beltsos, 2019, Journal of Assisted Reproduction and Genetics.

Latent Adeno-Associated Virus Infection Elicits Humoral but Not Cell-Mediated Immune Responses in a Nonhuman Primate Model

T. Flotte, A. Poirier, W. Kearns, 1999, Journal of Virology.

Model Immune Responses in a Nonhuman Primate Elicits Humoral but Not Cell-Mediated Latent Adeno-Associated Virus Infection

T. Flotte, A. Poirier, W. Kearns, 1999 .

The human embryonic genome is karyotypically complex, with chromosomally abnormal cells preferentially located away from the developing fetus.

Yulian Zhao, G. Cutting, P. Brezina, 2022, Human reproduction.

Essential learning tools for continuing medical education for physicians, geneticists, nurses, allied health professionals, mental health professionals, business administration professionals, and reproductive endocrinology and infertility (REI) fellows: the Midwest Reproductive Symposium Internation

W. Kearns, A. Beltsos, R. Jeelani, 2018, Journal of Assisted Reproduction and Genetics.

Single-gene testing combined with single nucleotide polymorphism microarray preimplantation genetic diagnosis for aneuploidy: a novel approach in optimizing pregnancy outcome.

S. Rechitsky, E. Pomerantseva, D. Pauling, 2011, Fertility and sterility.

Localization of the 70-kDa peroxisomal membrane protein to human 1p21-p22 and mouse 3.

D. Valle, W. Kearns, N. Copeland, 1993, Genomics.

SNP microarray genetic analyses to determine 23-chromosome ploidy, structural chromosome aberrations and genome-wide scans to identify disease risks from a single embryonic cell

A. Kittai, R. Leach, A. Benner, 2008 .

Protecting life in a time of war

D. Albertini, E. Telfer, W. Kearns, 2022, Journal of Assisted Reproduction and Genetics.

Preimplantation genetic testing

P. Brezina, W. Kearns, D. Brezina, 2012, BMJ : British Medical Journal.

Preimplantation Embryo Aneuploidy Rates in Couples Undergoing Donor Egg In Vitro Fertilization Cycles

J. Kaminsky, W. Kearns, K. Richter, 2005 .

Does theFMR1 gene affect IVF success?

M. Christianson, Bailey McGuinness, W. Kearns, 2019, Reproductive biomedicine online.