Enhanced interpretation of newborn screening results without analyte cutoff values.
Enhanced interpretation of newborn screening results without analyte cutoff values. [electronic resource] - Genetics in medicine : official journal of the American College of Medical Genetics Jul 2012 - 648-55 p. digital
Publication Type: Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
1530-0366
10.1038/gim.2012.2 doi
Computational Biology
Data Interpretation, Statistical
Databases, Factual
Diagnosis, Differential
False Positive Reactions
Humans
Infant, Newborn
International Cooperation
Metabolome
Minnesota
Multivariate Analysis
Neonatal Screening--methods
Pattern Recognition, Automated
Predictive Value of Tests
Retrospective Studies
Software
Tandem Mass Spectrometry--methods
Enhanced interpretation of newborn screening results without analyte cutoff values.
APA
Marquardt G., Currier R., McHugh D. M. S., Gavrilov D., Magera M. J., Matern D., Oglesbee D., Raymond K., Rinaldo P., Smith E. H., Tortorelli S., Turgeon C. T., Lorey F., Wilcken B., Wiley V., Greed L. C., Lewis B., Boemer F., Schoos R., Marie S., Vincent M., Sica Y. C., Domingos M. T., Al-Thihli K., Sinclair G., Al-Dirbashi O. Y., Chakraborty P., Dymerski M., Porter C., Manning A., Seashore M. R., Quesada J., Reuben A., Chrastina P., Hornik P., Atef Mandour I., Atty Sharaf S. A., Bodamer O., Dy B., Torres J., Zori R., Cheillan D., Vianey-Saban C., Ludvigson D., Stembridge A., Bonham J., Downing M., Dotsikas Y., Loukas Y. L., Papakonstantinou V., Zacharioudakis G. S. A., Baráth Á., Karg E., Franzson L., Jonsson J. J., Breen N. N., Lesko B. G., Berberich S. L., Turner K., Ruoppolo M., Scolamiero E., Antonozzi I., Carducci C., Caruso U., Cassanello M., la Marca G., Pasquini E., Di Gangi I. M., Giordano G., Camilot M., Teofoli F., Manos S. M., Peterson C. K., Mayfield Gibson S. K., Sevier D. W., Lee S., Park H., Khneisser I., Browning P., Gulamali-Majid F., Watson M. S., Eaton R. B., Sahai I., Ruiz C., Torres R., Seeterlin M. A., Stanley E. L., Hietala A., McCann M., Campbell C., Hopkins P. V., de Sain-Van der Velden M. G., Elvers B., Morrissey M. A., Sunny S., Knoll D., Webster D., Frazier D. M., McClure J. D., Sesser D. E., Willis S. A., Rocha H., Vilarinho L., John C., Lim J., Caldwell S. G., Tomashitis K., Castiñeiras Ramos D. E., Cocho de Juan J. A., Rueda Fernández I., Yahyaoui Macías R., Egea-Mellado J. M., González-Gallego I., Delgado Pecellin C., García-Valdecasas Bermejo M. S., Chien Y., Hwu W., Childs T., McKeever C. D., Tanyalcin T., Abdulrahman M., Queijo C., Lemes A., Davis T., Hoffman W., Baker M. & Hoffman G. L. (20130117). Enhanced interpretation of newborn screening results without analyte cutoff values. : Genetics in medicine : official journal of the American College of Medical Genetics.
Chicago
Marquardt Gregg, Currier Robert, McHugh David M S, Gavrilov Dimitar, Magera Mark J, Matern Dietrich, Oglesbee Devin, Raymond Kimiyo, Rinaldo Piero, Smith Emily H, Tortorelli Silvia, Turgeon Coleman T, Lorey Fred, Wilcken Bridget, Wiley Veronica, Greed Lawrence C, Lewis Barry, Boemer François, Schoos Roland, Marie Sandrine, Vincent Marie-Françoise, Sica Yuri Cleverthon, Domingos Mouseline Torquado, Al-Thihli Khalid, Sinclair Graham, Al-Dirbashi Osama Y, Chakraborty Pranesh, Dymerski Mark, Porter Cory, Manning Adrienne, Seashore Margretta R, Quesada Jonessy, Reuben Alejandra, Chrastina Petr, Hornik Petr, Atef Mandour Iman, Atty Sharaf Sahar Abdel, Bodamer Olaf, Dy Bonifacio, Torres Jasmin, Zori Roberto, Cheillan David, Vianey-Saban Christine, Ludvigson David, Stembridge Adrya, Bonham Jim, Downing Melanie, Dotsikas Yannis, Loukas Yannis L, Papakonstantinou Vagelis, Zacharioudakis Georgios S A, Baráth Ákos, Karg Eszter, Franzson Leifur, Jonsson Jon J, Breen Nancy N, Lesko Barbara G, Berberich Stanton L, Turner Kimberley, Ruoppolo Margherita, Scolamiero Emanuela, Antonozzi Italo, Carducci Claudia, Caruso Ubaldo, Cassanello Michela, la Marca Giancarlo, Pasquini Elisabetta, Di Gangi Iole Maria, Giordano Giuseppe, Camilot Marta, Teofoli Francesca, Manos Shawn M, Peterson Colleen K, Mayfield Gibson Stephanie K, Sevier Darrin W, Lee Soo-Youn, Park Hyung-Doo, Khneisser Issam, Browning Phaidra, Gulamali-Majid Fizza, Watson Michael S, Eaton Roger B, Sahai Inderneel, Ruiz Consuelo, Torres Rosario, Seeterlin Mary A, Stanley Eleanor L, Hietala Amy, McCann Mark, Campbell Carlene, Hopkins Patrick V, de Sain-Van der Velden Monique G, Elvers Bert, Morrissey Mark A, Sunny Sherlykutty, Knoll Detlef, Webster Dianne, Frazier Dianne M, McClure Julie D, Sesser David E, Willis Sharon A, Rocha Hugo, Vilarinho Laura, John Catharine, Lim James, Caldwell S Graham, Tomashitis Kathy, Castiñeiras Ramos Daisy E, Cocho de Juan Jose Angel, Rueda Fernández Inmaculada, Yahyaoui Macías Raquel, Egea-Mellado José María, González-Gallego Inmaculada, Delgado Pecellin Carmen, García-Valdecasas Bermejo Maria Sierra, Chien Yin-Hsiu, Hwu Wuh-Liang, Childs Thomas, McKeever Christine D, Tanyalcin Tijen, Abdulrahman Mahera, Queijo Cecilia, Lemes Aída, Davis Tim, Hoffman William, Baker Mei and Hoffman Gary L. 20130117. Enhanced interpretation of newborn screening results without analyte cutoff values. : Genetics in medicine : official journal of the American College of Medical Genetics.
Harvard
Marquardt G., Currier R., McHugh D. M. S., Gavrilov D., Magera M. J., Matern D., Oglesbee D., Raymond K., Rinaldo P., Smith E. H., Tortorelli S., Turgeon C. T., Lorey F., Wilcken B., Wiley V., Greed L. C., Lewis B., Boemer F., Schoos R., Marie S., Vincent M., Sica Y. C., Domingos M. T., Al-Thihli K., Sinclair G., Al-Dirbashi O. Y., Chakraborty P., Dymerski M., Porter C., Manning A., Seashore M. R., Quesada J., Reuben A., Chrastina P., Hornik P., Atef Mandour I., Atty Sharaf S. A., Bodamer O., Dy B., Torres J., Zori R., Cheillan D., Vianey-Saban C., Ludvigson D., Stembridge A., Bonham J., Downing M., Dotsikas Y., Loukas Y. L., Papakonstantinou V., Zacharioudakis G. S. A., Baráth Á., Karg E., Franzson L., Jonsson J. J., Breen N. N., Lesko B. G., Berberich S. L., Turner K., Ruoppolo M., Scolamiero E., Antonozzi I., Carducci C., Caruso U., Cassanello M., la Marca G., Pasquini E., Di Gangi I. M., Giordano G., Camilot M., Teofoli F., Manos S. M., Peterson C. K., Mayfield Gibson S. K., Sevier D. W., Lee S., Park H., Khneisser I., Browning P., Gulamali-Majid F., Watson M. S., Eaton R. B., Sahai I., Ruiz C., Torres R., Seeterlin M. A., Stanley E. L., Hietala A., McCann M., Campbell C., Hopkins P. V., de Sain-Van der Velden M. G., Elvers B., Morrissey M. A., Sunny S., Knoll D., Webster D., Frazier D. M., McClure J. D., Sesser D. E., Willis S. A., Rocha H., Vilarinho L., John C., Lim J., Caldwell S. G., Tomashitis K., Castiñeiras Ramos D. E., Cocho de Juan J. A., Rueda Fernández I., Yahyaoui Macías R., Egea-Mellado J. M., González-Gallego I., Delgado Pecellin C., García-Valdecasas Bermejo M. S., Chien Y., Hwu W., Childs T., McKeever C. D., Tanyalcin T., Abdulrahman M., Queijo C., Lemes A., Davis T., Hoffman W., Baker M. and Hoffman G. L. (20130117). Enhanced interpretation of newborn screening results without analyte cutoff values. : Genetics in medicine : official journal of the American College of Medical Genetics.
MLA
Marquardt Gregg, Currier Robert, McHugh David M S, Gavrilov Dimitar, Magera Mark J, Matern Dietrich, Oglesbee Devin, Raymond Kimiyo, Rinaldo Piero, Smith Emily H, Tortorelli Silvia, Turgeon Coleman T, Lorey Fred, Wilcken Bridget, Wiley Veronica, Greed Lawrence C, Lewis Barry, Boemer François, Schoos Roland, Marie Sandrine, Vincent Marie-Françoise, Sica Yuri Cleverthon, Domingos Mouseline Torquado, Al-Thihli Khalid, Sinclair Graham, Al-Dirbashi Osama Y, Chakraborty Pranesh, Dymerski Mark, Porter Cory, Manning Adrienne, Seashore Margretta R, Quesada Jonessy, Reuben Alejandra, Chrastina Petr, Hornik Petr, Atef Mandour Iman, Atty Sharaf Sahar Abdel, Bodamer Olaf, Dy Bonifacio, Torres Jasmin, Zori Roberto, Cheillan David, Vianey-Saban Christine, Ludvigson David, Stembridge Adrya, Bonham Jim, Downing Melanie, Dotsikas Yannis, Loukas Yannis L, Papakonstantinou Vagelis, Zacharioudakis Georgios S A, Baráth Ákos, Karg Eszter, Franzson Leifur, Jonsson Jon J, Breen Nancy N, Lesko Barbara G, Berberich Stanton L, Turner Kimberley, Ruoppolo Margherita, Scolamiero Emanuela, Antonozzi Italo, Carducci Claudia, Caruso Ubaldo, Cassanello Michela, la Marca Giancarlo, Pasquini Elisabetta, Di Gangi Iole Maria, Giordano Giuseppe, Camilot Marta, Teofoli Francesca, Manos Shawn M, Peterson Colleen K, Mayfield Gibson Stephanie K, Sevier Darrin W, Lee Soo-Youn, Park Hyung-Doo, Khneisser Issam, Browning Phaidra, Gulamali-Majid Fizza, Watson Michael S, Eaton Roger B, Sahai Inderneel, Ruiz Consuelo, Torres Rosario, Seeterlin Mary A, Stanley Eleanor L, Hietala Amy, McCann Mark, Campbell Carlene, Hopkins Patrick V, de Sain-Van der Velden Monique G, Elvers Bert, Morrissey Mark A, Sunny Sherlykutty, Knoll Detlef, Webster Dianne, Frazier Dianne M, McClure Julie D, Sesser David E, Willis Sharon A, Rocha Hugo, Vilarinho Laura, John Catharine, Lim James, Caldwell S Graham, Tomashitis Kathy, Castiñeiras Ramos Daisy E, Cocho de Juan Jose Angel, Rueda Fernández Inmaculada, Yahyaoui Macías Raquel, Egea-Mellado José María, González-Gallego Inmaculada, Delgado Pecellin Carmen, García-Valdecasas Bermejo Maria Sierra, Chien Yin-Hsiu, Hwu Wuh-Liang, Childs Thomas, McKeever Christine D, Tanyalcin Tijen, Abdulrahman Mahera, Queijo Cecilia, Lemes Aída, Davis Tim, Hoffman William, Baker Mei and Hoffman Gary L. Enhanced interpretation of newborn screening results without analyte cutoff values. : Genetics in medicine : official journal of the American College of Medical Genetics. 20130117.