Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Jigna Doshi"'
Publikováno v:
Molecular Diagnosis & Therapy
Background Lysis of maternal white blood cells in prenatal cell-free DNA (cfDNA) test samples increases the level of maternal DNA and consequently decreases fetal fraction. Objective The objective of this study was to determine whether hemolysis, tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebf0f0797c9d1b63e4e3413bf1e3c8e7
https://doi.org/10.1007/s40291-020-00446-x
https://doi.org/10.1007/s40291-020-00446-x
Autor:
Jacques Jani, Karen White, J de Marchin, Maximilian Schmid, S Conotte, Y. Wang, Jigna Doshi, K. Chen, Elisa Bevilacqua
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 55:132-133
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6616ea3e42b6bea642b471050207ff9f
https://doi.org/10.1002/uog.20366
https://doi.org/10.1002/uog.20366
Autor:
Renee Stokowski, Jigna Doshi, Elisa Bevilacqua, Susie Wang, Eric Wang, Andrew B. Sparks, P. Bogard, Coleen R. Hacker, Jennifer A. Kaplan, Jacques Jani, Maximilian Schmid, Karen White
Publikováno v:
Fetal diagnosis and therapy, 44 (4
Objective: To determine the performance of a targeted microarray-based cell-free DNA (cfDNA) test (Harmony Prenatal Test®) for the identification of pregnancies at increased risk for 22q11.2 deletion. Methods: Test performance was determined in 2 st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51881f66c0aab054d208cc2008f1736c
https://pubmed.ncbi.nlm.nih.gov/29131052
https://pubmed.ncbi.nlm.nih.gov/29131052
Autor:
H. Chuang, K. Chen, Maximilian Schmid, Liza Kunz, Jigna Doshi, Karen White, Jacques Jani, Renee Stokowski, Y. Wang, Elisa Bevilacqua
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 54:156-156
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf934f003664883f2771e325220a5e62
https://doi.org/10.1002/uog.20877
https://doi.org/10.1002/uog.20877
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 54:99-99
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f5146537f8c58844e8dd0ded2472375
https://doi.org/10.1002/uog.20690
https://doi.org/10.1002/uog.20690
Autor:
Naiping Shen, Michel Sun, Andrew B. Sparks, Ken Song, Jill Garrison, Patrick Pattee, Aoy Tomita-Mitchell, Craig A. Struble, Jacob Zahn, Jay Sandler, Celeste McBride, Renee Stokowski, John R. Stuelpnagel, Desiree Hollemon, Kevin J. Lee, Michael S Mitchell, Arnold Oliphant, Eric T. Wang, Wade A. Barrett, Jigna Doshi
Publikováno v:
Prenatal Diagnosis. 32:3-9
Objective To develop a novel prenatal assay based on selective analysis of cell-free DNA in maternal blood for evaluation of fetal Trisomy 21 (T21) and Trisomy 18 (T18). Methods Two hundred ninety-eight pregnancies, including 39 T21 and seven T18 con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b60729464798b8ef2efd8e510ef2ec9a
https://doi.org/10.1002/pd.2922
https://doi.org/10.1002/pd.2922
Autor:
Kelly A. Frazer, Nila Patil, Mark Trulson, Michael Norris, David L. Stern, Kanan R. Vyas, Bich T. N. Nguyen, David R. Cox, Daryl J. Thomas, Renee Stokowski, David A. Hinds, Jigna Doshi, John B. Sheehan, Claire Marjoribanks, Naiping Shen, Wade A. Barrett, Stephen P. A. Fodor, Coleen R. Hacker, Danny H. Lee, Curtis Kautzer, David P. McDonough, Anthony Berno
Publikováno v:
Science. 294:1719-1723
Global patterns of human DNA sequence variation (haplotypes) defined by common single nucleotide polymorphisms (SNPs) have important implications for identifying disease associations and human traits. We have used high-density oligonucleotide arrays,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b36b5997a4d619ec7f096e5ec033ba8c
https://doi.org/10.1126/science.1065573
https://doi.org/10.1126/science.1065573
Autor:
Andrew B, Sparks, Eric T, Wang, Craig A, Struble, Wade, Barrett, Renee, Stokowski, Celeste, McBride, Jacob, Zahn, Kevin, Lee, Naiping, Shen, Jigna, Doshi, Michel, Sun, Jill, Garrison, Jay, Sandler, Desiree, Hollemon, Patrick, Pattee, Aoy, Tomita-Mitchell, Michael, Mitchell, John, Stuelpnagel, Ken, Song, Arnold, Oliphant
Publikováno v:
Prenatal diagnosis. 32(1)
To develop a novel prenatal assay based on selective analysis of cell-free DNA in maternal blood for evaluation of fetal Trisomy 21 (T21) and Trisomy 18 (T18).Two hundred ninety-eight pregnancies, including 39 T21 and seven T18 confirmed fetal aneupl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c7ad818b07707c3f30d5de9936062930
https://pubmed.ncbi.nlm.nih.gov/22616698
https://pubmed.ncbi.nlm.nih.gov/22616698
Autor:
Andrew D. Sparks, Ken Song, Craig A. Struble, Patrick Pattee, Jay Sandler, Renee Stokowski, Wade A. Barrett, Jill Garrison, Celeste McBride, Michel Sun, Jacob Zahn, Naiping Shen, Desiree Hollemon, Eric Wang, John R. Stuelpnagel, Jigna Doshi, Kevin J. Lee, Arnold Oliphant
Publikováno v:
American Journal of Obstetrics and Gynecology. 206:S314-S315
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf580c51b5757b74d26551c5d813116b
https://doi.org/10.1016/j.ajog.2011.10.725
https://doi.org/10.1016/j.ajog.2011.10.725