Gail Stetten

Research output

Research output per year 1970 1988 1991 1992 1993 1997 1998 1999 2008 2013

• 85 Article
• 4 Review article

Research output per year

Research output per year

Search results

• 2013

  In utero hematopoietic stem cell transplantation in canines: Exploring the gestational age window of opportunity to maximize engraftment

  Petersen, S. M., Gendelman, M., Murphy, K. M., Torbenson, M., Jones, R. J., Stetten, G., Bird, C. & Blakemore, K. J., 2013, In: Fetal Diagnosis and Therapy. 33, 2, p. 116-121 6 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Hematopoietic Stem Cell Transplantation 100%
  • Chimerism 87%
  • Canidae 81%
  • Gestational Age 80%
  • Transplants 29%
  9 Scopus citations
• 2011

  X-linked adrenoleukodystrophy: ABCD1 de novo mutations and mosaicism

  Wang, Y., Busin, R., Reeves, C., Bezman, L., Raymond, G., Toomer, C. J., Watkins, P. A., Snowden, A., Moser, A., Naidu, S., Bibat, G., Hewson, S., Tam, K., Clarke, J. T. R., Charnas, L., Stetten, G., Karczeski, B., Cutting, G. & Steinberg, S., Sep 2011, In: Molecular genetics and metabolism. 104, 1-2, p. 160-166 7 p.

  Research output: Contribution to journal › Article › peer-review

  • Adrenoleukodystrophy 100%
  • Mosaicism 84%
  • Mutation 58%
  • Mothers 37%
  • Grandparents 25%
  29 Scopus citations
• 2008

  Clinical consequences of an increasing trend of preferential use of cultured villi for molecular diagnosis by CVS

  Aina-Mumuney, A., Wood, E. D., Corson, V. L., Stetten, G., Jari, S., Boehm, C. D. & Blakemore, K. J., Apr 2008, In: Prenatal Diagnosis. 28, 4, p. 332-334 3 p.

  Research output: Contribution to journal › Article › peer-review

  • Chorionic Villi Sampling 100%
  • Cultured Cells 47%
  • Prenatal Diagnosis 42%
  • Gestational Age 36%
  • DNA 31%
  3 Scopus citations

• Prenatal detection of a subtle unbalanced chromosome rearrangement by karyotyping, FISH and array comparative genomic hybridization

  Cain, C. C., Saul, D. O., Oehler, E., Blakemore, K. & Stetten, G., Oct 2008, In: Fetal Diagnosis and Therapy. 24, 3, p. 286-290 5 p.

  Research output: Contribution to journal › Article › peer-review

  • Karyotyping 100%
  • Comparative Genomic Hybridization 93%
  • Chromosomes 61%
  • Chromosomes, Human, Pair 2 51%
  • Fetus 46%
  13 Scopus citations

• Prenatal diagnosis of mosaic trisomy 8q studied by ultrasound, cytogenetics, and array-CGH

  Wood, E., Dowey, S., Saul, D., Cain, C., Rossiter, J., Blakemore, K. & Stetten, G., Mar 15 2008, In: American Journal of Medical Genetics, Part A. 146, 6, p. 764-769 6 p.

  Research output: Contribution to journal › Article › peer-review

  • Trisomy 8q Chromosome 8 100%
  • Comparative Genomic Hybridization 61%
  • Prenatal Diagnosis 51%
  • Trisomy Chromosome 8 51%
  • Cytogenetics 50%
  9 Scopus citations

• X inactivation in triploidy and trisomy: The search for autosomal transfactors that choose the active X

  Migeon, B. R., Pappas, K., Stetten, G., Trunca, C. & Jacobs, P. A., Feb 2008, In: European Journal of Human Genetics. 16, 2, p. 153-162 10 p.

  Research output: Contribution to journal › Article › peer-review

  • Triploidy 100%
  • X Chromosome Inactivation 90%
  • X Chromosome 78%
  • Chromosomes, Human, Pair 19 24%
  • Chromosomes, Human, Pair 5 23%
  12 Scopus citations
• 2007

  Microphthalmia with linear skin defects (MLS) syndrome evaluated by prenatal karyotyping, FISH and array comparative genomic hybridization

  Cain, C. C., Saul, D., Attanasio, L., Oehler, E., Hamosh, A., Blakemore, K. & Stetten, G., Apr 2007, In: Prenatal Diagnosis. 27, 4, p. 373-379 7 p.

  Research output: Contribution to journal › Article › peer-review

  • Syndromic 7 Microphthalmia 100%
  • Karyotyping 63%
  • Comparative Genomic Hybridization 59%
  • Karyotype 50%
  • Microphthalmos 28%
  8 Scopus citations

• Use of T-cell antibodies for donor dosaging in a canine model of in utero hematopoietic stem cell transplantation

  Petersen, S. M., Gendelman, M., Murphy, K. M., Torbenson, M., Jones, R. J., Althaus, J. E., Stetten, G., Bird, C. & Blakemore, K. J., Apr 2007, In: Fetal Diagnosis and Therapy. 22, 3, p. 175-179 5 p.

  Research output: Contribution to journal › Article › peer-review

  • Hematopoietic Stem Cell Transplantation 100%
  • Chimerism 93%
  • Canidae 81%
  • Graft vs Host Disease 59%
  • T-Lymphocytes 57%
  16 Scopus citations
• 2006

  Frequency of chromosomal abnormalities in spontaneous abortions derived from intracytoplasmic sperm injection compared with those from in vitro fertilization

  Ma, S., Philipp, T., Zhao, Y., Stetten, G., Robinson, W. P. & Kalousek, D., Jan 2006, In: Fertility and sterility. 85, 1, p. 236-239 4 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Aneuploidy 91%
  • Fertilization in Vitro 91%
  • Spontaneous Abortion 88%
  • Chromosome Aberrations 81%
  19 Scopus citations

• Redefining the risks of prenatally ascertained supernumerary marker chromosomes: A collaborative study

  Graf, M. D., Christ, L., Mascarello, J. T., Mowrey, P., Pettenati, M., Stetten, G., Storto, P., Surti, U., Van Dyke, D. L., Vance, G. H., Wolff, D. & Schwartz, S., Aug 2006, In: Journal of medical genetics. 43, 8, p. 660-664 5 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Chromosomes, Human, 1-3 100%
  • Genetic Markers 59%
  • Cytogenetics 18%
  • Phenotype 11%
  • Karyotype 9%
  46 Scopus citations
• 2005

  A reciprocal translocation 46,XY,t(8;9)(p11.2;q13) in a bladder exstrophy patient disrupts CNTNAP3 and presents evidence of a pericentromeric duplication on chromosome 9

  Boyadjiev, S. A., South, S. T., Radford, C. L., Patel, A., Zhang, G., Hur, D. J., Thomas, G. H., Gearhart, J. P. & Stetten, G., May 2005, In: Genomics. 85, 5, p. 622-629 8 p.

  Research output: Contribution to journal › Article › peer-review

  • Bladder Exstrophy 100%
  • Chromosomes, Human, Pair 9 89%
  • Chromosome Breakpoints 70%
  • Clone Cells 53%
  • Fluorescence In Situ Hybridization 45%
  20 Scopus citations

• Autopsy findings of a 37-year-old man with a complex mosaic karyotype involving del(18p), monosomy 13, and trisomy 20

  Halushka, M. K., Stetten, G., McMichael, J. L., Blakemore, K. J. & Hutchins, G. M., Jun 1 2005, In: American Journal of Medical Genetics. 135 A, 2, p. 181-185 5 p.

  Research output: Contribution to journal › Article › peer-review

  • Trisomy Chromosome 20 100%
  • Karyotype 56%
  • Cerebellum 50%
  • Autopsy 46%
  • Olivary Nucleus 42%
  1 Scopus citations

• Prenatal detection of an interstitial deletion in 4p15 in a fetus with an increased nuchal skin fold measurement

  South, S. T., Corson, V. L., McMichael, J. L., Blakemore, K. J. & Stetten, G., 2005, In: Fetal Diagnosis and Therapy. 20, 1, p. 58-63 6 p.

  Research output: Contribution to journal › Article › peer-review

  • Nuchal Translucency Measurement 100%
  • Chromosome 4 short arm deletion 79%
  • Fetus 56%
  • Skin 39%
  • Chromosome Deletion 11%
  4 Scopus citations
• 2004

  In utero hematopoietic stem cell transplantation with haploidentical donor adult bone marrow in a canine model

  Blakemore, K., Hattenburg, C., Stetten, G., Berg, K., South, S., Murphy, K., Jones, R. & Lockwood, C. J., Apr 2004, In: American journal of obstetrics and gynecology. 190, 4, p. 960-971 12 p.

  Research output: Contribution to journal › Article › peer-review

  • Chimerism 100%
  • Hematopoietic Stem Cell Transplantation 85%
  • Canidae 69%
  • Bone Marrow Transplantation 61%
  • Bone Marrow 58%
  33 Scopus citations

• Reevaluating confined placental mosaicism.

  Stetten, G., Escallon, C. S., South, S. T., McMichael, J. L., Saul, D. O. & Blakemore, K. J., Dec 15 2004, In: American journal of medical genetics. Part A. 131, 3, p. 232-239 8 p.

  Research output: Contribution to journal › Article › peer-review

  • Mosaicism 100%
  • Chorionic Villi 26%
  • Pregnancy 24%
  • Cytogenetic Analysis 23%
  • Genetic Counseling 22%
  41 Scopus citations

• Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of Down syndrome

  Kahlem, P., Sultan, M., Herwig, R., Steinfath, M., Balzereit, D., Eppens, B., Saran, N. G., Pletcher, M. T., South, S. T., Stetten, G., Lehrach, H., Reeves, R. H. & Yaspo, M. L., Jul 2004, In: Genome research. 14, 7, p. 1258-1267 10 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Gene Dosage 100%
  • Chromosomes, Human, Pair 21 87%
  • Down Syndrome 87%
  • Genes 33%
  • Chromosomes 13%
  193 Scopus citations
• 2001

  Non-mosaic trisomy 20 presenting at 21 weeks' gestation as a thoraco-abdominal mass

  Driggers, R. W., Bernstein, H., Lantz, M., Stetten, G., Escallon, C. S., Perlman, E. & Blakemore, K. J., 2001, In: Prenatal Diagnosis. 21, 5, p. 387-389 3 p.

  Research output: Contribution to journal › Article › peer-review

  • Trisomy Chromosome 20 100%
  • Fetus 44%
  • Pregnancy 33%
  • Autopsy 31%
  • Bronchopulmonary Sequestration 26%
  6 Scopus citations

• Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel

  Tuck-Muller, C. M., Goodman, B. K., Li, S., Martinez, J. E., Chen, X. N., Wertelecki, W., Korenberg, J. R. & Stetten, G., 2001, In: Genetics in Medicine. 3, 2, p. 126-131 6 p.

  Research output: Contribution to journal › Article › peer-review

  • Trisomy 7p Chromosome 7 100%
  • Bacterial Artificial Chromosomes 70%
  • Clone Cells 40%
  • Chromosomes 39%
  • Fluorescence In Situ Hybridization 21%
  1 Scopus citations
• 2000

  A Cre-lox recombination system for the targeted integration of circular yeast artificial chromosomes into embryonic stem cells

  Call, L. M., Moore, C. S., Stetten, G. & Gearhart, J. D., 2000, In: Human molecular genetics. 9, 12, p. 1745-1751 7 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Yeast Artificial Chromosomes 100%
  • Systems Integration 95%
  • Embryonic Stem Cells 70%
  • Genetic Recombination 64%
  • Transgenes 25%
  22 Scopus citations

• Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: Karyotype-phenotype correlations

  Wallerstein, R., Yu, M. T., Neu, R. L., Benn, P., Bowen, C. L., Crandall, B., Disteche, C., Donahue, R., Harrison, B., Hershey, D., Higgins, R. R., Jenkins, L. S., Jackson-Cook, C., Keitges, E., Khodr, G., Lin, C. C., Luthardt, F. W., Meisner, L., Mengden, G., Patil, S. R., & 9 othersRodriguez, M., Sciorra, L. J., Shaffer, L. G., Stetten, G., Van Dyke, D. L., Wang, H., Williams, F., Zaslav, A. L. & Hsu, L. Y. F., 2000, In: Prenatal Diagnosis. 20, 2, p. 103-122 20 p.

  Research output: Contribution to journal › Article › peer-review

  • Chromosomes, Human, Pair 18 100%
  • Chromosomes, Human, Pair 13 96%
  • Chromosomes, Human, Pair 21 95%
  • Mosaicism 89%
  • Karyotype 74%
  70 Scopus citations

• Human PRRX1 and PRRX2 genes: Cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome

  Norris, R. A., Scott, K. K., Moore, C. S., Stetten, G., Brown, C. R., Jabs, E. W., Wulfsberg, E. A., Yu, J. & Kern, M. J., 2000, In: Mammalian Genome. 11, 11, p. 1000-1005 6 p.

  Research output: Contribution to journal › Article › peer-review

  • Nager type Acrofacial dysostosis 100%
  • Organism Cloning 50%
  • Gene Expression 32%
  • Genes 21%
  • Genee-Wiedemann syndrome 17%
  37 Scopus citations
• 1999

  Cloning and characterization of a secreted frizzled-related protein that is expressed by the retinal pigment epithelium

  Chang, J. T., Esumi, N., Moore, K., Li, Y., Zhang, S., Chew, C., Goodman, B., Rattner, A., Moody, S., Stetten, G., Campochiaro, P. A. & Zack, D. J., 1999, In: Human molecular genetics. 8, 4, p. 575-583 9 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • WD repeat containing planar cell polarity effector 100%
  • Retinal Pigment Epithelium 71%
  • Organism Cloning 57%
  • Retina 54%
  • human SFRP5 protein 30%
  90 Scopus citations

• Integration of cytogenetic with recombinational and physical maps of mouse chromosome 16

  Moore, C. S., Lee, J. S., Birren, B., Stetten, G., Baxter, L. L. & Reeves, R. H., Jul 1 1999, In: Genomics. 59, 1, p. 1-5 5 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Chromosomes, Human, Pair 16 100%
  • Fluorescence In Situ Hybridization 74%
  • Cytogenetics 72%
  • Interphase 28%
  • Clone Cells 19%
  26 Scopus citations

• Molecular cytogenetic analysis and clinical findings in a newborn with prenatally diagnosed rec(7)dup(7q)inv(7)(p22q31.3)pat

  Goodman, B. K., Stone, K., Coddett, J. M., Cargile, C. B., Gurewitsch, E. D., Blakemore, K. J. & Stetten, G., 1999, In: Prenatal Diagnosis. 19, 12, p. 1150-1156 7 p.

  Research output: Contribution to journal › Article › peer-review

  • Trisomy 7q Chromosome 7 100%
  • Cytogenetic Analysis 60%
  • Newborn Infant 39%
  • Cerebral Ventricles 33%
  • Chromosomes, Human, Pair 7 33%
  11 Scopus citations

• Revised genomic organization of FBN1 and significance for regulated gene expression

  Biery, N. J., Eldadah, Z. A., Moore, C. S., Stetten, G., Spencer, F. & Dietz, H. C., Feb 15 1999, In: Genomics. 56, 1, p. 70-77 8 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Fibrillin-1 100%
  • Exons 55%
  • Gene Expression 39%
  • Swine 34%
  • Marfan Syndrome 28%
  79 Scopus citations

• X-linked adrenoleukodystrophy: Genes, mutations, and phenotypes

  Smith, K. D., Kemp, S., Braiterman, L. T., Lu, J. F., Wei, H. M., Geraghty, M., Stetten, G., Bergin, J. S., Pevsner, J. & Watkins, P. A., 1999, In: Neurochemical Research. 24, 4, p. 521-535 15 p.

  Research output: Contribution to journal › Article › peer-review

  • Adrenoleukodystrophy 100%
  • X-Linked Genes 87%
  • long-chain-fatty-acid-CoA ligase 83%
  • Mutation 58%
  • Carrier Proteins 48%
  145 Scopus citations
• 1998

  Genomic structure of PEX13, a candidate peroxisome biogenesis disorder gene

  Björkman, J., Stetten, G., Moore, C. S., Gould, S. J. & Crane, D. I., Dec 15 1998, In: Genomics. 54, 3, p. 521-528 8 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Peroxisome biogenesis disorders 100%
  • Genes 23%
  • Peroxisome-Targeting Signal 1 Receptor 21%
  • Proteins 21%
  • Chromosomes, Human, Pair 2 15%
  14 Scopus citations

• Isolation and characterization of the human gene encoding I(to): Further diversity by alternative mRNA splicing

  Kong, W., Po, S., Yamagishi, T., Ashen, M. D., Stetten, G. & Tomaselli, G. F., Dec 1998, In: American Journal of Physiology - Heart and Circulatory Physiology. 275, 6 44-6, p. H1963-H1970

  Research output: Contribution to journal › Article › peer-review

  • Alternative Splicing 100%
  • Messenger RNA 52%
  • Protein Kinase C 43%
  • Action Potentials 41%
  • Mammals 40%
  72 Scopus citations

• Isolation and characterization of the human gene encoding Ito: Further diversity by alternative mRNA splicing

  Kong, W., Po, S., Yamagishi, T., Ashen, M. D., Stetten, G. & Tomaselli, G. F., Dec 1998, In: American Journal of Physiology - Heart and Circulatory Physiology. 44, 6

  Research output: Contribution to journal › Article › peer-review

  • Alternative Splicing 100%
  • Messenger RNA 52%
  • Protein Kinase C 43%
  • Action Potentials 41%
  • Mammals 40%

• Map location and gene structure of the Homo sapiens mitotic arrest deficient 2 (MAD2L1) gene at 4q27

  Krishnan, R., Goodman, B., Jin, D. Y., Jeang, K. T., Collins, C., Stetten, G. & Spencer, F., May 1 1998, In: Genomics. 49, 3, p. 475-478 4 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access
  14 Scopus citations

• Region-specific fish probes used to identify and characterize and interstitial paracentric inv(21)(q22.1q22.3)

  Torchia, B. S., Escallon, C., Blakemore, K. J. & Stetten, G., Aug 1998, In: Prenatal Diagnosis. 18, 8, p. 849-853 5 p.

  Research output: Contribution to journal › Article › peer-review

  • Chromosomes, Human, Pair 21 100%
  • Fishes 70%
  • Chromosome Painting 59%
  • Amniocentesis 46%
  • Genetic Counseling 41%
  3 Scopus citations
• 1997

  A paternally derived inverted duplication of 7q with evidence of a telomeric deletion

  Stetten, G., Charity, L. L., Kasch, L. M., Scott, A. F., Berman, C. L., Pressman, E. & Blakemore, K. J., Jan 10 1997, In: American journal of medical genetics. 68, 1, p. 76-81 6 p.

  Research output: Contribution to journal › Article › peer-review

  • Trisomy 7q Chromosome 7 100%
  • Chromosomes, Human, Pair 7 66%
  • Second Pregnancy Trimester 27%
  • Hydrocephalus 27%
  • Karyotype 26%
  25 Scopus citations

• Immunolocalization of CENP-A suggests a distinct nucleosome structure at the inner kinetochore plate of active centromeres

  Warburton, P. E., Cooke, C. A., Bourassa, S., Vafa, O., Sullivan, B. A., Stetten, G., Gimelli, G., Warburton, D., Tyler-Smith, C., Sullivan, K. F., Poirier, G. G. & Earnshaw, W. C., Nov 1 1997, In: Current Biology. 7, 11, p. 901-904 4 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • kinetochores 100%
  • Kinetochores 99%
  • nucleosomes 92%
  • Centromere 91%
  • Nucleosomes 88%
  284 Scopus citations

• New cytogenetic technology and its application in maternal-fetal medicine

  Stetten, G., Goodman, B. K. & Fox, H. E., Dec 1 1997, In: Journal of Maternal-Fetal Investigation. 7, 4, p. 155-162 8 p.

  Research output: Contribution to journal › Review article › peer-review
  1 Scopus citations

• Segregation of a familial balanced (12;10) insertion resulting in dup(10)(q21.2q22.1) and Del(10)(q21.2q22.1) in First cousins

  Doheny, K. F., Rasmussen, S. A., Rutberg, J., Semenza, G. L., Stamberg, J., Schwartz, M., Batista, D. A. S., Stetten, G. & Thomas, G. H., Mar 17 1997, In: American journal of medical genetics. 69, 2, p. 188-193 6 p.

  Research output: Contribution to journal › Article › peer-review

  • Chromosomes, Human, Pair 10 100%
  • Telecanthus 65%
  • Chromosome Painting 59%
  • Heart Murmurs 51%
  • Chromosomes, Human, Pair 12 51%
  9 Scopus citations
• 1996

  Alterations of yeast artificial chromosome transgenic sequences in stretched embryonic stem-cell chromatin visualized by fluorescence in situ hybridization

  Rosenberg, C., Voltz, A. K., Lamb, B. T., Stetten, G. & Gearhart, J. D., Jan 1 1996, In: Cytogenetics and cell genetics. 75, 1, p. 67-70 4 p.

  Research output: Contribution to journal › Article › peer-review

  • Yeast Artificial Chromosomes 100%
  • Embryonic Stem Cells 70%
  • Fluorescence In Situ Hybridization 67%
  • Chromatin 58%
  • Transgenic Mice 29%
  5 Scopus citations

• Ambiguous genitalia in an elderly woman with a mosaic 45,X/46,X,DIC(Y)(Q11.2) karyotype

  Smith, Y. R., Stetten, G., Charity, L., Isacson, C., Gearhart, J. P. & Namnoum, A. B., Feb 1996, In: Urology. 47, 2, p. 259-262 4 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Disorders of Sex Development 100%
  • Dacarbazine 95%
  • Y Chromosome 90%
  • Inguinal Hernia 87%
  • Karyotype 76%
  12 Scopus citations

• Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: A collaborative study

  Hsu, L. Y. F., Yu, M. T., Richkind, K. E., Van Dyke, D. L., Crandall, B. F., Saxe, D. F., Khodr, G. S., Mennuti, M., Stetten, G., Miller, W. A. & Priest, J. H., Jan 1996, In: Prenatal Diagnosis. 16, 1, p. 1-28 28 p.

  Research output: Contribution to journal › Article › peer-review

  • Mosaicism 100%
  • Amniocentesis 99%
  • Chromosomes 64%
  • Phenotype 48%
  • Chromosome 19 ring 45%
  85 Scopus citations
• 1995

  An accessory marker derived from chromosome 20 and its co‐existence with a mosaic trisomy 20 cell line

  Batista, D. A. S., Escallon, C., Blakemore, K. J. & Stetten, G., Feb 1995, In: Prenatal Diagnosis. 15, 2, p. 123-127 5 p.

  Research output: Contribution to journal › Article › peer-review

  • Trisomy Chromosome 20 100%
  • Ring Chromosomes 84%
  • Chromosomes, Human, Pair 20 81%
  • Failure to Thrive 70%
  • Karyotype 56%
  15 Scopus citations

• Molecular characterization of a deleted X chromosome (Xq13.3-Xq21.31) exhibiting random X inactivation

  Migeon, B. R., Stetten, G., Tuck-Muller, C., Axelman, J., Jani, M. & Dungy, D., Mar 1995, In: Somatic Cell and Molecular Genetics. 21, 2, p. 113-120 8 p.

  Research output: Contribution to journal › Article › peer-review

  • X Chromosome Inactivation 100%
  • X Chromosome 86%
  • Chromosomes 30%
  • Chromosomes, Human, X 14%
  • Fibroblasts 14%
  3 Scopus citations

• TRPC1, a human homolog of a Drosophila store-operated channel

  Wes, P. D., Chevesich, J., Jeromin, A., Rosenberg, C., Stetten, G. & Montell, C., Oct 10 1995, In: Proceedings of the National Academy of Sciences of the United States of America. 92, 21, p. 9652-9656 5 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Transient Receptor Potential Channels 100%
  • Drosophila 71%
  • Proteins 28%
  • Vertebrates 22%
  • Light Signal Transduction 18%
  477 Scopus citations
• 1994

  Molecular analysis of a complex chromosomal rearrangement and a review of familial cases

  Batista, D. A. S., Pai, G. S. & Stetten, G., 1994, In: American journal of medical genetics. 53, 3, p. 255-263 9 p.

  Research output: Contribution to journal › Article › peer-review

  • Chromosomes 100%
  • Chromosomes, Human, Pair 13 24%
  • Chromosomes, Human, Pair 7 23%
  • Mentally Disabled Persons 22%
  • Telomere 19%
  100 Scopus citations

• Nonrandom inactivation of the Y-bearing X chromosome in a 46, XX individual: Evidence for the etiology of 46, XX true hermaphroditism

  Fechner, P. Y., Rosenberg, C., Stetten, G., Cargile, C. B., Pearson, P. L., Smith, K. D., Migeon, C. J. & Berkovitz, G. D., 1994, In: Cytogenetics and cell genetics. 66, 1, p. 22-261 240 p.

  Research output: Contribution to journal › Article › peer-review

  • Ovotesticular Disorders of Sex Development 100%
  • X Chromosome 67%
  • In Situ Hybridization 13%
  • Testis 13%
  • X Chromosome Inactivation 9%
  31 Scopus citations

• Unilateral Renal Hypoplasia And Contralateral Renal Agenesis: A New Association With 45,X/46,XY Mosaicism

  Wax, J., Prabhakar, G., Giraldez, R., Hutchins, G., Stetten, G. & Blakemore, K., May 1994, In: American journal of perinatology. 11, 3, p. 184-186 3 p.

  Research output: Contribution to journal › Article › peer-review

  • Hereditary renal agenesis 100%
  • Solitary Kidney 89%
  • Turner Syndrome 87%
  • Mosaicism 84%
  • Oligohydramnios 71%
  2 Scopus citations
• 1993

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

  Batista, D. A. S., Tuck-Muller, C. M., Martinez, J. E., Kearns, W. G., Pearson, P. L. & Stetten, G., Sep 1993, In: Human genetics. 92, 2, p. 117-121 5 p.

  Research output: Contribution to journal › Article › peer-review

  • Fluorescence In Situ Hybridization 100%
  • Cytogenetics 48%
  • Chromosome Aberrations 47%
  • Chromosomes 39%
  43 Scopus citations

• Prenatal cytogenetic analysis of the fetus

  Stetten, G., Jan 1 1993, In: Obstetrics and Gynecology Clinics of North America. 20, 3, p. 433-442 10 p.

  Research output: Contribution to journal › Review article › peer-review

  • Chorionic Villi 100%
  • Cytogenetic Analysis 88%
  • Amniotic Fluid 81%
  • Fetus 59%
  • Cell Count 56%
  1 Scopus citations

• Rapid diagnosis of trisomy 18 and dizygosity in twins using fluorescence in situ hybridization on uncultured amniocytes

  Blakemore, K. J., Rosenberg, C., Jaswaney, V. L., Pressman, E. K., Kearns, W. G., Pearson, P. L. & Stetten, G., 1993, In: Journal of Maternal-Fetal and Neonatal Medicine. 2, 4, p. 197-200 4 p.

  Research output: Contribution to journal › Article › peer-review

  • Trisomy 18 Syndrome 100%
  • Twins 77%
  • Fluorescence In Situ Hybridization 73%
  • Cytogenetics 71%
  • Amniocentesis 59%

• The role of the sex-determining region Y gene in the etiology of 46,XX maleness

  Fechner, P. Y., Marcantonio, S. M., Jaswaney, V., Stetten, G., Goodfellow, P. N., Migeon, C. J., Smith, K. D., Berkovitz, G. D., Amrhein, J. A., Bard, P. A., Lee, P. A., Reid, C., Tsalikian, E. & Urban, M. D., Mar 1993, In: Journal of Clinical Endocrinology and Metabolism. 76, 3, p. 690-695 6 p.

  Research output: Contribution to journal › Article › peer-review

  • sry Genes 100%
  • Heterogeneity 55%
  • Y Chromosome 55%
  • Genetic Heterogeneity 35%
  • X Chromosome 34%
  90 Scopus citations

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

  McGinniss, M. J., Rosenberg, C., Stetten, G., Schinzel, A. A., Binkert, F., Petersen, M. B., Kearns, W. G., Kazazian, H. H., Pearson, P. L. & Antonarakis, S. E., 1993, In: American journal of medical genetics. 46, 6, p. 647-651 5 p.

  Research output: Contribution to journal › Article › peer-review

  • Chromosome 21 ring 100%
  • Chromosome 18 deletion syndrome 93%
  • Chromosomes, Human, Pair 21 66%
  • Fluorescence In Situ Hybridization 51%
  • Chromosomes, Human, Pair 18 46%
  3 Scopus citations
• 1992

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

  Rosenberg, C., Blakemore, K. J., Kearns, W. G., Giraldez, R. A., Escallon, C. S., Pearson, P. L. & Stetten, G., Apr 1992, In: American journal of human genetics. 50, 4, p. 700-705 6 p.

  Research output: Contribution to journal › Article › peer-review

  • Chromosome Painting 100%
  • Chromosomes 51%
  • Gene Library 17%
  • Fluorescence In Situ Hybridization 16%
  • Cytogenetics 15%
  37 Scopus citations