C. Ris-Stalpers

发表

Early enteral tube feeding in optimizing treatment of hyperemesis gravidarum: the Maternal and Offspring outcomes after Treatment of HyperEmesis by Refeeding (MOTHER) randomized controlled trial.

B. Mol, C. Naaktgeboren, T. Roseboom, 2017, The American journal of clinical nutrition.

Creatine kinase inhibition lowers systemic arterial blood pressure in spontaneously hypertensive rats: a randomized controlled trial

Joseph F. Clark, A. V. van Kuilenburg, L. Brewster, 2016, Journal of hypertension.

A mutation in the ligand binding domain of the androgen receptor of human LNCaP cells affects steroid binding characteristics and response to anti-androgens.

G. Jenster, J. Veldscholte, J. Trapman, 1990, Biochemical and biophysical research communications.

Genetic Analyses in Small-for-Gestational-Age Newborns

R. Hennekam, J. Wit, N. Solanky, 2018, The Journal of clinical endocrinology and metabolism.

Physiology and pathophysiology of the DUOXes.

C. Ris-Stalpers, 2006, Antioxidants & redox signaling.

Placental iodothyronine deiodinase III and II ratios, mRNA expression compared to enzyme activity

C. Ris-Stalpers, J. D. Vijlder, M. Stulp, 1998, Molecular and Cellular Endocrinology.

An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito

S. Verhoef, A. V. D. van den Ouweland, D. Halley, 2000, Journal of medical genetics.

Plasma thyrotropin bioactivity in Down's syndrome children with subclinical hypothyroidism.

C. Ris-Stalpers, J. de Vijlder, T. Vulsma, 2001, European journal of endocrinology.

Plasma ceramide is increased and associated with proteinuria in women with pre-eclampsia and HELLP syndrome.

C. Chalfant, C. Ris-Stalpers, B. H. van den Born, 2019, Pregnancy hypertension.

Two frequent missense mutations in Pendred syndrome.

E. Green, C. Cremers, N. Dietrich, 1998, Human molecular genetics.

Hyperemesis gravidarum severity, enteral tube feeding and cardiometabolic markers in offspring cord blood

T. Roseboom, I. Grooten, Marjette H. Koot, 2022, British Journal of Nutrition.

Genes differentially expressed in thyroid carcinoma identified by comparison of SAGE expression profiles

C. Ris-Stalpers, J. Smit, E. Pauws, 2004, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Absence of activating mutations in ras and gsp oncogenes in a cohort of nine patients with sporadic pediatric thyroid tumors.

C. Ris-Stalpers, J. D. Vijlder, J. de Vijlder, 2001, Medical and pediatric oncology.

Meta-Analysis of Placental Transcriptome Data Identifies a Novel Molecular Pathway Related to Preeclampsia

D. Enquobahrie, P. Moerland, J. V. D. van der Post, 2015, PloS one.

Total bile acids in the maternal and fetal compartment in relation to placental ABCG2 expression in preeclamptic pregnancies complicated by HELLP syndrome.

J. V. D. van der Post, C. Ris-Stalpers, R. Elferink, 2015, Biochimica et biophysica acta.

Seven placental transcripts characterize HELLP-syndrome.

A. V. van Kampen, J. V. D. van der Post, C. Ris-Stalpers, 2008, Placenta.

Serial analysis of gene expression as a tool to assess the human thyroid expression profile and to identify novel thyroidal genes.

F. Baas, C. Ris-Stalpers, M. Tijssen, 2000, The Journal of clinical endocrinology and metabolism.

In silico analysis of the Mus musculus uterine gene expression landscape during pregnancy identifies putative upstream regulators for labour

J. V. D. van der Post, C. Ris-Stalpers, A. Jongejan, 2018, PloS one.

Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in Israelis

J. Sack, C. Ris-Stalpers, S. Refetoff, 2007, Clinical endocrinology.

A premature stopcodon in thyroglobulin messenger RNA results in familial goiter and moderate hypothyroidism.

C. Ris-Stalpers, M. Cammenga, H. Targovnik, 1999, The Journal of clinical endocrinology and metabolism.

Structure, function, and relevance of thyroid peroxidase in inherited diseases of the thyroid

C. Ris-Stalpers, J. de Vijlder, T. Vulsma, 1997 .

Up to date with human thyroglobulin.

C. Ris-Stalpers, H. Targovnik, J. de Vijlder, 2001, The Journal of endocrinology.

Cardiovascular biochemical risk factors among women with spontaneous preterm delivery

B. Mulder, A. Franx, J. V. D. van der Post, 2018, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

Expression of Placental FLT1 Transcript Variants Relates to Both Gestational Hypertensive Disease and Fetal Growth

J. V. D. van der Post, C. Ris-Stalpers, G. Afink, 2011, Hypertension.

Expression of Placental FLT 1 Transcript Variants Relates to Both Gestational Hypertensive Disease and Fetal Growth

C. Ris-Stalpers, G. Afink, R. Keijser, 2011 .

Structural organization of the human androgen receptor gene.

J. A. van der Korput, J. Trapman, C. Ris-Stalpers, 1989, Journal of molecular endocrinology.

Maternal cardiac function, uteroplacental Doppler flow parameters and pregnancy outcome: a systematic review

J. Aarnoudse, C. Ris-Stalpers, D. V. van Veldhuisen, 2015, Ultrasound in Obstetrics and Gynecology.

SFlt-1 Elevates Blood Pressure by Augmenting Endothelin-1-Mediated Vasoconstriction in Mice

J. V. D. van der Post, C. Ris-Stalpers, B. H. van den Born, 2014, PloS one.

A premature stopcodon in thyroglobulin messenger RNA results in familial goiter and moderate hypothyroidism.

C. Ris-Stalpers, M. Cammenga, H. Targovnik, 1999, The Journal of clinical endocrinology and metabolism.

Depression, anxiety, and post-traumatic stress disorder symptoms after hyperemesis gravidarum: a prospective cohort study

T. Roseboom, I. Grooten, Marjette H. Koot, 2022, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Aberrant splicing of androgen receptor mRNA results in synthesis of a nonfunctional receptor protein in a patient with androgen insensitivity.

J. Trapman, C. Ris-Stalpers, A. Brinkmann, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Extending the scope of pooled analyses of individual patient biomarker data from heterogeneous laboratory platforms and cohorts using merging algorithms.

L. Poston, R. Ness, E. Steegers, 2016, Pregnancy hypertension.

The screening for mutations in the thyroglobulin cDNA from six patients with congenital hypothyroidism.

C. Ris-Stalpers, M. Cammenga, J. Orgiazzi, 1999, Biochimie.

The revised 8307 base pair coding sequence of human thyroglobulin transiently expressed in eukaryotic cells.

C. Ris-Stalpers, J. de Vijlder, E. Pauws, 1997, European journal of endocrinology.

Increased glucocerebrosidase expression and activity in preeclamptic placenta.

E. Ver Loren van Themaat, P. Moerland, J. V. D. van der Post, 2015, Placenta.

Expression of the alpha 1, alpha 2, and beta 1 T3-receptor mRNAs in the fasted rat measured using competitive PCR.

W. Wiersinga, C. Ris-Stalpers, O. Bakker, 1998, Biochemical and biophysical research communications.

[65-OR]: Total bile acids in the maternal and fetal compartment in relation to placental ABCG2 expression in preeclamptic pregnancy.

C. Ris-Stalpers, G. Afink, A. Kremer, 2015 .

TBX2, a Novel Regulator of Labour

J. V. D. van der Post, C. Ris-Stalpers, M. Oudijk, 2021, Medicina.

Soluble syndecan-1 and glycosaminoglycans in preeclamptic and normotensive pregnancies

C. Ris-Stalpers, B. H. van den Born, N. van Vlies, 2021, Scientific Reports.

The Role of Phosphatidylinositol Transfer Proteins (PITPs) in Intracellular Signalling

Tengyu Ma, J. Veldscholte, C. Ris-Stalpers, 1998 .

Autotaxin activity has a high accuracy to diagnose intrahepatic cholestasis of pregnancy.

J. V. D. van der Post, C. Ris-Stalpers, U. Beuers, 2015, Journal of hepatology.

Differential splicing of human androgen receptor pre-mRNA in X-linked Reifenstein syndrome, because of a deletion involving a putative branch site.

J. Trapman, C. Ris-Stalpers, A. Brinkmann, 1994, American journal of human genetics.

Accuracy of circulating placental growth factor, vascular endothelial growth factor, soluble fms‐like tyrosine kinase 1 and soluble endoglin in the prediction of pre‐eclampsia: a systematic review and meta‐analysis

C. Ris-Stalpers, P. von Dadelszen, E. Pajkrt, 2012, BJOG : an international journal of obstetrics and gynaecology.

Unique skin changes in a case of Albright hereditary osteodystrophy caused by a rare GNAS1 mutation

E. Blom, C. Ris-Stalpers, A. C. Nieuwenhuijzen Kruseman, 2010, The British journal of dermatology.

HELLP syndrome preceded by intrahepatic cholestasis of pregnancy: one serious itch

M. Tabbers, J. V. D. van der Post, C. Ris-Stalpers, 2014, BMJ Case Reports.

Molecular genetics of preeclampsia and HELLP syndrome - a review.

J. V. D. van der Post, C. Ris-Stalpers, G. Afink, 2012, Biochimica et biophysica acta.

The androgen receptor in LNCaP cells contains a mutation in the ligand binding domain which affects steroid binding characteristics and response to antiandrogens

G. Jenster, J. Veldscholte, J. Trapman, 1992, Journal of Steroid Biochemistry and Molecular Biology.

Androgen receptor mutations

G. Jenster, J. Trapman, C. Ris-Stalpers, 1995, The Journal of Steroid Biochemistry and Molecular Biology.

Type II and type III deiodinase activity in human placenta as a function of gestational age.

T. Visser, C. Ris-Stalpers, J. de Vijlder, 1996, The Journal of clinical endocrinology and metabolism.

Active caspase-3 is removed from cells by release of caspase-3-enriched vesicles.

J. Stap, C. V. van Noorden, R. Nieuwland, 2013, Biochimica et biophysica acta.

Genetic basis of hypothyroidism: recent advances, gaps and strategies for future research

C. Ris-Stalpers, J. Moreno, J. D. Vijlder, 2003, Trends in Endocrinology & Metabolism.

Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidism.

F. Baas, M. Kempers, C. Ris-Stalpers, 2002, The New England journal of medicine.

Characterization of a novel loss‐of‐function mutation of PAX8 associated with congenital hypothyroidism

P. Macchia, M. Zannini, C. Ris-Stalpers, 2010, Clinical endocrinology.

The Clinical and Molecular Relations Between Idiopathic Preterm Labor and Maternal Congenital Heart Defects

B. Mulder, C. Ris-Stalpers, V. Christoffels, 2013, Reproductive Sciences.

Androgen receptor abnormalities

J. Trapman, C. Ris-Stalpers, A. Brinkmann, 1991, The Journal of Steroid Biochemistry and Molecular Biology.

Pathophysiological aspects of thyroid hormone disorders/thyroid peroxidase autoantibodies and reproduction.

E. Fliers, C. Ris-Stalpers, M. Goddijn, 2015, Human reproduction update.

Masayuki Yamamoto, I. Trougakos, D. Chartoumpekis, 2018, Thyroid : official journal of the American Thyroid Association.

Inborn errors of thyroid hormone biosynthesis.

C. Ris-Stalpers, J. de Vijlder, T. Vulsma, 1997, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

The idiopathic preterm delivery methylation profile in umbilical cord blood DNA

J. V. D. van der Post, C. Ris-Stalpers, M. Mannens, 2015, BMC Genomics.

The role of extracellular matrix in normal and pathological pregnancy: Future applications of microphysiological systems in reproductive medicine

Benjamin D. Pope, K. Parker, C. Ris-Stalpers, 2020, Experimental biology and medicine.

The androgen receptor: Functional structure and expression in transplanted human prostate tumors and prostate tumor cell lines

J. Trapman, C. Ris-Stalpers, A. Brinkmann, 1990, The Journal of Steroid Biochemistry and Molecular Biology.

Heterogeneity in polyadenylation cleavage sites in mammalian mRNA sequences: implications for SAGE analysis.

E Pauws, A. V. van Kampen, C. Ris-Stalpers, 2001, Nucleic acids research.

STOX1 is not imprinted and is not likely to be involved in preeclampsia

S. Apostolidou, P. Stanier, C. Ris-Stalpers, 2007, Nature Genetics.

UvA-DARE ( Digital Academic Repository ) The role of autotaxin in cholestatic pruritus

C. Ris-Stalpers, U. Beuers, R. Elferink, 2017 .

On the origin of circulating thyroglobulin.

C. Ris-Stalpers, J. de Vijlder, T. Vulsma, 1999, European journal of endocrinology.

Cloning of tissue-specific genes using serial analysis of gene expression and a novel computational substraction approach.

A. V. van Kampen, A. V. Kampen, C. Ris-Stalpers, 2001, Genomics.

Determinants of disease course and severity in hyperemesis gravidarum.

M. Leeflang, B. Mol, T. Roseboom, 2019, European journal of obstetrics, gynecology, and reproductive biology.

Early nasogastric tube feeding in optimising treatment for hyperemesis gravidarum: the MOTHER randomised controlled trial (Maternal and Offspring outcomes after Treatment of HyperEmesis by Refeeding)

B. Mol, T. Roseboom, I. Grooten, 2016, BMC Pregnancy and Childbirth.

Resistance Artery Creatine Kinase mRNA and Blood Pressure in Humans

Joseph F. Clark, L. Brewster, G. V. van Montfrans, 2014, Hypertension.

Hydrogen sulfide producing enzymes in pregnancy and preeclampsia.

H. van Goor, C. Ris-Stalpers, M. Faas, 2012, Placenta.

[94-OR]: Extending the scope of individual patient data meta-analyses: Merging algorithms for biomarker measurements from heterogeneous laboratory platforms. The CoLAB Preeclampsia angiogenic factor study.

L. Poston, R. Ness, E. Steegers, 2015 .

Thyroid‐stimulating hormone and free thyroxine fail to predict the severity and clinical course of hyperemesis gravidarum: A prospective cohort study

B. Mol, C. Naaktgeboren, T. Roseboom, 2021, Acta obstetricia et gynecologica Scandinavica.

Differentially Expressed Genes in the Pre-Eclamptic Placenta: A Systematic Review and Meta-Analysis

Miranda van Uitert, P. Moerland, J. V. D. van der Post, 2013, PloS one.

Recurrence, postponing pregnancy, and termination rates after hyperemesis gravidarum: Follow up of the MOTHER study

B. Mol, T. Roseboom, I. Grooten, 2021, Acta obstetricia et gynecologica Scandinavica.

Ketonuria is not associated with hyperemesis gravidarum disease severity.

C. Naaktgeboren, T. Roseboom, I. Grooten, 2020, European journal of obstetrics, gynecology, and reproductive biology.

Higher decidual EBI3 and HLA-G mRNA expression in preeclampsia: Cause or consequence of preeclampsia.

J. V. D. van der Post, C. Ris-Stalpers, S. Scherjon, 2016, Human immunology.

Structure and Function of the Human Androgen Receptor

G. Jenster, J. Trapman, C. Ris-Stalpers, 1992 .

Substitution of aspartic acid-686 by histidine or asparagine in the human androgen receptor leads to a functionally inactive protein with altered hormone-binding characteristics.

G. Jenster, J. Trapman, C. Ris-Stalpers, 1991, Molecular endocrinology.

Successful transfer to sulfonylurea therapy in an infant with developmental delay, epilepsy and neonatal diabetes (DEND) syndrome and a novel ABCC8 gene mutation

C. Ris-Stalpers, A. S. Slingerland, N. Zwaveling-Soonawala, 2010, Diabetologia.

Importance of the content and localization of tyrosine residues for thyroxine formation within the N-terminal part of human thyroglobulin.

C. Ris-Stalpers, J. de Vijlder, O. Bakker, 1995, European journal of endocrinology.

Molecular basis of androgen insensitivity

G. Jenster, J. Trapman, C. Ris-Stalpers, 1996, Steroids.

Genetics and phenomics of hypothyroidism and goiter due to TPO mutations

C. Ris-Stalpers, H. Bikker, 2010, Molecular and Cellular Endocrinology.

Molecular characterization of iodotyrosine dehalogenase deficiency in patients with hypothyroidism.

C. Ris-Stalpers, A. V. van Cruchten, G. Afink, 2008, The Journal of clinical endocrinology and metabolism.

A Practical Approach to the Detection of Androgen Receptor Gene Mutations and Pedigree Analysis in Families with X-Linked Androgen Insensitivity

J. Oosterwijk, J. Trapman, D. Halley, 1994, Pediatric Research.

Initial characterization of C16orf89, a novel thyroid-specific gene.

C. Meischl, C. Ris-Stalpers, G. Afink, 2010, Thyroid : official journal of the American Thyroid Association.

H9c2 cardiomyoblasts produce thyroid hormone.

W. Paulus, H. Buermans, M. Blankenstein, 2008, American journal of physiology. Cell physiology.

H 9 c 2 cardiomyoblasts produce thyroid hormone

W. Paulus, H. Buermans, M. Blankenstein, 2008 .

A novel homeobox gene overexpressed in thyroid carcinoma.

C. Ris-Stalpers, E. Pauws, Gwendolyn G Sijmons, 2004, Thyroid : official journal of the American Thyroid Association.

Expression of an Aberrantly Spliced Androgen Receptor mRNA in a Family with Complete Androgen Insensitivity a

J. Trapman, C. Ris-Stalpers, A. Brinkmann, 1993, Annals of the New York Academy of Sciences.

The idiopathic preterm delivery methylation profile in umbilical cord blood DNA

J. V. D. van der Post, C. Ris-Stalpers, M. Mannens, 2015, BMC Genomics.

Vaccination from the early second trimester onwards gives a robust SARS-CoV-2 antibody response throughout pregnancy and provides antibodies for the neonate

C. D. de Groot, M. V. van Gils, C. Ris-Stalpers, 2023, International Journal of Infectious Diseases.

Accuracy of Circulating Placental Growth Factor, Vascular Endothelial Growth Factor, Soluble fms-like Tyrosine Kinase-1, and Soluble Endoglin in the Prediction of Preeclampsia: A Systematic Review and Meta-Analysis

P. Bossuyt, B. Mol, C. Ris-Stalpers, 2013 .

The Clinical and Molecular Relations Between Idiopathic Preterm Labor and Maternal Congenital Heart Defects

B. Mulder, C. Ris-Stalpers, V. Christoffels, 2013, Reproductive Sciences.