نتائج البحث - "Marike Polak"

المساهمون: Clinical genetics, APH - Personalized Medicine, APH - Quality of Care, Amsterdam Reproduction & Development, Human genetics, Amsterdam Reproduction & Development (AR&D), Clinical Genetics, Department of Life Sciences, Research Methods and Techniques

المصدر: European Journal of Human Genetics. Nature Publishing Group
European Journal of Human Genetics, 31(4), 409-416. Nature Publishing Group
Houtman, D, Vijlbrief, B, Polak, M, Pot, J, Verhoef, P, Cornel, M & Riedijk, S 2022, ' Changes in opinions about human germline gene editing as a result of the Dutch DNA-dialogue project ', European Journal of Human Genetics . https://doi.org/10.1038/s41431-022-01114-wTest

مصطلحات موضوعية: SDG 3 - Good Health and Well-being, Genetics, Genetics (clinical)

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1bde4760ea634926737a20f4a63b3cfTest
http://www.scopus.com/inward/record.url?scp=85129837017&partnerID=8YFLogxKTest

6

The Multidimensional Wellbeing in Youth Scale (MWYS): Development and Psychometric Properties_Datasets

المؤلفون: Kayla Green, Suzanne van de Groep, Renske van der Cruijsen, Marike Polak, Eveline A. Crone

مصطلحات موضوعية: Child and adolescent development, Psychological methodology, design and analysis, Testing, assessment and psychometrics, Adolescence, Youth, Young adulthood, Wellbeing, Mental health, Questionnaire, Survey, Assessment, Youth participation, Co-creation

العلاقة: https://figshare.com/articles/dataset/The_Multidimensional_Wellbeing_in_Youth_Scale_MWYS_Development_and_Psychometric_Properties_Datasets/21988796Test

الإتاحة: https://doi.org/10.25397/eur.21988796.v1Test
https://figshare.com/articles/dataset/The_Multidimensional_Wellbeing_in_Youth_Scale_MWYS_Development_and_Psychometric_Properties_Datasets/21988796Test

View record in BASE

7

The potential diagnostic yield of whole exome sequencing in pregnancies complicated by fetal ultrasound anomalies

المؤلفون: Grazia M.S. Mancini, Kathleen Romijn, Alice S. Brooks, Hennie T. Brüggenwirth, Marjon van Slegtenhorst, Ingrid M.B.H. van de Laar, Lutgarde C.P. Govaerts, Joan N.R. Kromosoeto, Malgorzata I. Srebniak, Robert-Jan H. Galjaard, Marike Polak, Diane Van Opstal, Attie T.J.I. Go, Yolande van Bever, Lies H. Hoefsloot, Marieke Joosten, Martina Wilke, Maarten F. C. M. Knapen, Karin E. M. Diderich

المساهمون: Clinical Genetics, Research Methods and Techniques, Obstetrics & Gynecology

المصدر: Acta Obstetricia et Gynecologica Scandinavica, 100(6), 1-10. Wiley-Blackwell
Acta Obstetricia et Gynecologica Scandinavica

مصطلحات موضوعية: Adult, medicine.medical_specialty, Microarray, Genetic counseling, Chromosome Disorders, Prenatal diagnosis, Ultrasonography, Prenatal, whole exome sequencing, 03 medical and health sciences, 0302 clinical medicine, Pregnancy, Prenatal Diagnosis, Exome Sequencing, ultrasound anomalies, medicine, Humans, Abnormalities, Multiple, Genetic Testing, Original Research Article, fetal anomalies, 030212 general & internal medicine, Exome, Exome sequencing, Retrospective Studies, prenatal whole exome sequencing testing, Fetus, 030219 obstetrics & reproductive medicine, Obstetrics, business.industry, Genetic disorder, Obstetrics and Gynecology, Retrospective cohort study, General Medicine, medicine.disease, Fetal Diseases, diagnostic yield, Female, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04ae4bf0f35164bb766af6f4fd8ffc0bTest
https://hdl.handle.net/1765/132863Test

8

Factors involved in the decision to decline prenatal screening with noninvasive prenatal testing (NIPT)

المؤلفون: Lisanne, van Prooyen Schuurman, Karuna, van der Meij, Nicolien, van Ravesteyn, Neeltje, Crombag, Janneke, Gitsels-van der Wal, Caroline, Kooij, Linda, Martin, Ingrid, Peters, Marike, Polak, Elsbeth, van Vliet-Lachotzki, Robert-Jan, Galjaard, Lidewij, Henneman

المساهمون: Human genetics, Amsterdam Reproduction & Development (AR&D), Midwifery Science, APH - Quality of Care, Public Health, Clinical Genetics, Obstetrics & Gynecology, Research Methods and Techniques

المصدر: van Prooyen Schuurman, L, van der Meij, KRM, van Ravesteyn, N T, Kooij, C, Gitsels-van der Wal, JT, Martin, L, Peters, I M, Polak, M, van Vliet-Lachotzki, E H, Galjaard, R-J H & Henneman, L 2022, ' Factors involved in the decision to decline prenatal screening with noninvasive prenatal testing (NIPT) ', Prenatal Diagnosis . https://doi.org/10.1002/pd.6242Test
Prenatal Diagnosis. John Wiley and Sons Ltd
Prenatal Diagnosis, 43(4), 467-476. John Wiley & Sons Ltd.

مصطلحات موضوعية: Genetics & Heredity, Science & Technology, ANEUPLOIDY, NETHERLANDS, Obstetrics & Gynecology, WOMEN, Obstetrics and Gynecology, DIAGNOSIS, CELL-FREE DNA, SOCIOECONOMIC-STATUS, KNOWLEDGE, DOWN-SYNDROME, Life Sciences & Biomedicine, Genetics (clinical)

وصف الملف: Print-Electronic; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f61a7c880dae9a86e550c0539e8add3Test
http://www.scopus.com/inward/record.url?scp=85138701625&partnerID=8YFLogxKTest

9

Nuchal translucency of 3.0-3.4 mm an indication for NIPT or microarray? Cohort analysis and literature review

المؤلفون: Malgorzata I. Srebniak, Olav Bjørn Petersen, Karin E. M. Diderich, Diane Van Opstal, Marike Polak, Maarten F. C. M. Knapen, Caterina M. Bilardo, Eric Smith, Lidia R. Arends, Ida Vogel

المساهمون: Clinical Genetics, Research Methods and Techniques, Obstetrics & Gynecology

المصدر: Petersen, O B, Smith, E, Van Opstal, D, Polak, M, Knapen, M F C M, Diderich, K E M, Bilardo, C M, Arends, L R, Vogel, I & Srebniak, M I 2020, ' Nuchal translucency of 3.0-3.4 mm an indication for NIPT or microarray? Cohort analysis and literature review ', Acta Obstetricia et Gynecologica Scandinavica, vol. 99, no. 6, pp. 765-774 . https://doi.org/10.1111/aogs.13877Test
Acta Obstetricia et Gynecologica Scandinavica, 99(6), 765-774. Wiley-Blackwell
Acta Obstetricia et Gynecologica Scandinavica

مصطلحات موضوعية: medicine.medical_specialty, non‐invasive prenatal test, 1ST TRIMESTER, Microarray, Noninvasive Prenatal Testing, DUTCH LABORATORIES, Trisomy, Prenatal diagnosis, Chromosome aberration, Article, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Nuchal translucency, Pregnancy, CHROMOSOMAL MICROARRAY, THICKNESS, medicine, Humans, non-invasive prenatal test, Original Research Article, 030212 general & internal medicine, Retrospective Studies, nuchal translucency, Chromosome Aberrations, RISK, 030219 obstetrics & reproductive medicine, prenatal diagnosis, Obstetrics, business.industry, ANEUPLOIDY, STATEMENT, Obstetrics and Gynecology, Retrospective cohort study, General Medicine, NORMAL KARYOTYPE, Microarray Analysis, medicine.disease, Residual risk, ARRAY, Female, microdeletion, Nuchal Translucency Measurement, business, submicroscopic chromosomal abnormalities, SINGLETON PREGNANCIES, microarray, Cohort study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::178348a4b64eeb8c0b1e1659712cf67eTest
https://doi.org/10.1111/aogs.13877Test

10

Personality Functioning in Obesity and Binge Eating Disorder: Combining a Psychodynamic and Trait Perspective

المؤلفون: Theo J. M. Ingenhoven, Jack Dekker, Laura Van Riel, Elske van den Berg, Marike Polak, Jaap Peen, Marjolein M. Geerts

المساهمون: Research Methods and Techniques, Neurology, Other Research

المصدر: Journal of Psychiatric Practice, 26(6), 472-484. Lippincott Williams & Wilkins
Journal of psychiatric practice, 26(6), 472-484. Lippincott Williams and Wilkins

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1d6103ba030c0d99b815f2942c7f365Test
https://doi.org/10.1097/PRA.0000000000000513Test

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