| Title | Author | Year | SCOPUS | PUBMED | ISI | TCI | |
|---|---|---|---|---|---|---|---|
| 1. | Maternal isodisomy for chromosome 2p causing severe congenital hypothyroidism | B Bakker H Bikker RCM Hennekam EJP Lommen MGJ Schipper T Vulsma JJM de Vijlder |
2001 | ||||
| 2. | High incidence of thyroid dysfunction despite prophylaxis with potassium iodide during I-131-meta-iodobenzylguanidine treatment in children with neuroblastoma | HM van Santen J de Kraker BLF van Eck JJM de Vijlder T Vulsma |
2002 | ||||
| 3. | Longitudinal analysis of growth and puberty in 21-hydroxylase deficiency patients | HJ Van der Kamp BJ Otten N Buitenweg SMPFD Keizer-Schrama W Oostdijk M Jansen HA Delemarre-de Waal T Vulsma JM Wit |
2002 | ||||
| 4. | Lower neonatal screening thyroxine concentrations in Down syndrome newborns | ASP van Trotsenburg T Vulsma HM van Santen W Cheung JJM de Vijlder |
2003 | ||||
| 5. | No damaging effect of chemotherapy in addition to radiotherapy on the thyroid axis in young adult survivors of childhood cancer | HM van Santen T Vulsma MG Dijkgraaf RME Blumer R Heinen MWM Jaspers MM Geenen MO Offringa JJM de Vijlder C van den Bos |
2003 | ||||
| 6. | The effect of thyroxine treatment started in the neonatal period on development and growth of two-year-old Down syndrome children: A randomized clinical trial | ASP van Trotsenburg T Vulsma SLR van Rozenburg-Marres AL van Baar JCD Ridder HSA Heymans JGP Tijssen JJM de Vijlder |
2005 | ||||
| 7. | Neonatal screening for congenital hypothyroidism based on thyroxine, thyrotropin, and thyroxine-binding globulin measurement: Potentials and pitfalls | M. J. E. Kempers C. I. Lanting A. F. J. van Heijst A. S. P. van Trotsenburg B. M. Wiedijk J. J. M. de Vijlder T. Vulsma |
2006 | ||||
| 8. | Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement | Yu Sun Beata Bak Nadia Schoenmakers A. S. Paul van Trotsenburg Wilma Oostdijk Peter Voshol Emma Cambridge Jacqueline K. White Paul le Tissier S. Neda Mousavy Gharavy Juan P. Martinez-Barbera Wilhelmina H. Stokvis-Brantsma Thomas Vulsma Marlies J. Kempers Luca Persani Irene Campi Marco Bonomi Paolo Beck-Peccoz Hongdong Zhu Timothy M. E. Davis Anita C. S. Hokken-Koelega Dania Gorbenko Del Blanco Jayanti J. Rangasami Claudia A. L. Ruivenkamp Jeroen F. J. Laros Marjolein Kriek Sarina G. Kant Cathy A. J. Bosch Nienke R. Biermasz Natasha M. Appelman-Dijkstra Eleonora P. Corssmit Guido C. J. Hovens Alberto M. Pereira Johan T. den Dunnen Michael G. Wade Martijn H. Breuning Raoul C. Hennekam Krishna Chatterjee Mehul T. Dattani Jan M. Wit Daniel J. Bernard |
2012 | ||||
| 9. | Loss-of-function mutations in the immunoglobulin superfamily member 1 gene (IGSF1) cause a novel, X-linked syndrome of central hypothyroidism and testicular enlargement | N. Schoenmakers Y. Sun B. Bak A. S. P. van Trotsenburg W. Oostdijk P. Voshol E. Cambridge J. K. White P. le Tissier S. N. M. Gharavy J. P. Martinez-Barbera W. H. Stokvis-Brantsma T. Vulsma M. J. Kempers L. Persani I. Campi M. Bonomi P. Beck-Peccoz H. Zhu T. M. E. Davis A. C. S. Hokken-Koelega D. Gorbenko Del Blanco J. J. Rangasami C. A. L. Ruivenkamp J. F. J. Laros M. Kriek S. G. Kant C. A. J. Bosch N. R. Biermasz N. M. Appelman-Dijkstra E. P. Corssmit G. C. J. Hovens A. M. Pereira J. T. den Dunnen M. G. Wade M. H. Breuning R. C. Hennekam M. T. Dattani J. M. Wit D. J. Bernard K. Chatterjee |
2013 | ||||
| 10. | Neurodevelopmental retardation, as assessed clinically and with magnetoencephalography and electroencephalography, associated with perinatal dioxin exposure | G. W. ten Tusscher M. M. Leijs L. C. C. de Boer J. Legler K. Olie H. Spekreijse B. W. van Dijk T. Vulsma J. Briet A. Ilsen J. G. Koppe |
2014 | ||||
| 11. | Changes in body mass index in long-term childhood cancer survivors | Hanneke M. van Santen Ronald B. Geskus Steven Raemaekers A. S. Paul van Trotsenburg Thomas Vulsma Helena J. H. van der Pal Hubert N. Caron Leontien C. M. Kremer |
2015 | Count | 0 | 0 | 11 | 0 |
| Title | Authors | Year | Publication name | Cited count | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| < 2017 | 2018 | 2019 | 2020 | 2021 | 2022 | รวม | ||||||
| Title | Authors | Year | Journal title |
|---|
| Title | Authors | Year | Journal title | Cited count | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| < 2017 | 2018 | 2019 | 2020 | 2021 | 2022 | รวม | ||||||
| 1. | Maternal isodisomy for chromosome 2p causing severe congenital hypothyroidism | B Bakker H Bikker RCM Hennekam EJP Lommen MGJ Schipper T Vulsma JJM de Vijlder |
2001 |
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM 3.0 (86.0), pp. 1164.0-1168.0 |
38 | 0 | 0 | 0 | 0 | 0 | 38 | |
| 2. | High incidence of thyroid dysfunction despite prophylaxis with potassium iodide during I-131-meta-iodobenzylguanidine treatment in children with neuroblastoma | HM van Santen J de Kraker BLF van Eck JJM de Vijlder T Vulsma |
2002 |
CANCER 7.0 (94.0), pp. 2081.0-2089.0 |
38 | 0 | 0 | 0 | 0 | 0 | 38 | |
| 3. | Longitudinal analysis of growth and puberty in 21-hydroxylase deficiency patients | HJ Van der Kamp BJ Otten N Buitenweg SMPFD Keizer-Schrama W Oostdijk M Jansen HA Delemarre-de Waal T Vulsma JM Wit |
2002 |
ARCHIVES OF DISEASE IN CHILDHOOD 2.0 (87.0), pp. 139.0-144.0 |
39 | 0 | 0 | 0 | 0 | 0 | 39 | |
| 4. | Lower neonatal screening thyroxine concentrations in Down syndrome newborns | ASP van Trotsenburg T Vulsma HM van Santen W Cheung JJM de Vijlder |
2003 |
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM 4.0 (88.0), pp. 1512.0-1515.0 |
47 | 0 | 0 | 0 | 0 | 0 | 47 | |
| 5. | No damaging effect of chemotherapy in addition to radiotherapy on the thyroid axis in young adult survivors of childhood cancer | HM van Santen T Vulsma MG Dijkgraaf RME Blumer R Heinen MWM Jaspers MM Geenen MO Offringa JJM de Vijlder C van den Bos |
2003 |
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM 8.0 (88.0), pp. 3657.0-3663.0 |
36 | 0 | 0 | 0 | 0 | 0 | 36 | |
| 6. | The effect of thyroxine treatment started in the neonatal period on development and growth of two-year-old Down syndrome children: A randomized clinical trial | ASP van Trotsenburg T Vulsma SLR van Rozenburg-Marres AL van Baar JCD Ridder HSA Heymans JGP Tijssen JJM de Vijlder |
2005 |
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM 6.0 (90.0), pp. 3304.0-3311.0 |
49 | 0 | 0 | 0 | 0 | 0 | 49 | |
| 7. | Neonatal screening for congenital hypothyroidism based on thyroxine, thyrotropin, and thyroxine-binding globulin measurement: Potentials and pitfalls | M. J. E. Kempers C. I. Lanting A. F. J. van Heijst A. S. P. van Trotsenburg B. M. Wiedijk J. J. M. de Vijlder T. Vulsma |
2006 |
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM 9.0 (91.0), pp. 3370.0-3376.0 |
40 | 0 | 0 | 0 | 0 | 0 | 40 | |
| 8. | Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement | Yu Sun Beata Bak Nadia Schoenmakers A. S. Paul van Trotsenburg Wilma Oostdijk Peter Voshol Emma Cambridge Jacqueline K. White Paul le Tissier S. Neda Mousavy Gharavy Juan P. Martinez-Barbera Wilhelmina H. Stokvis-Brantsma Thomas Vulsma Marlies J. Kempers Luca Persani Irene Campi Marco Bonomi Paolo Beck-Peccoz Hongdong Zhu Timothy M. E. Davis Anita C. S. Hokken-Koelega Dania Gorbenko Del Blanco Jayanti J. Rangasami Claudia A. L. Ruivenkamp Jeroen F. J. Laros Marjolein Kriek Sarina G. Kant Cathy A. J. Bosch Nienke R. Biermasz Natasha M. Appelman-Dijkstra Eleonora P. Corssmit Guido C. J. Hovens Alberto M. Pereira Johan T. den Dunnen Michael G. Wade Martijn H. Breuning Raoul C. Hennekam Krishna Chatterjee Mehul T. Dattani Jan M. Wit Daniel J. Bernard |
2012 |
NATURE GENETICS 12.0 (44.0), pp. 1375.0-1381.0 |
47 | 0 | 0 | 0 | 0 | 0 | 47 | |
| 9. | Loss-of-function mutations in the immunoglobulin superfamily member 1 gene (IGSF1) cause a novel, X-linked syndrome of central hypothyroidism and testicular enlargement | N. Schoenmakers Y. Sun B. Bak A. S. P. van Trotsenburg W. Oostdijk P. Voshol E. Cambridge J. K. White P. le Tissier S. N. M. Gharavy J. P. Martinez-Barbera W. H. Stokvis-Brantsma T. Vulsma M. J. Kempers L. Persani I. Campi M. Bonomi P. Beck-Peccoz H. Zhu T. M. E. Davis A. C. S. Hokken-Koelega D. Gorbenko Del Blanco J. J. Rangasami C. A. L. Ruivenkamp J. F. J. Laros M. Kriek S. G. Kant C. A. J. Bosch N. R. Biermasz N. M. Appelman-Dijkstra E. P. Corssmit G. C. J. Hovens A. M. Pereira J. T. den Dunnen M. G. Wade M. H. Breuning R. C. Hennekam M. T. Dattani J. M. Wit D. J. Bernard K. Chatterjee |
2013 |
LANCET (381.0), pp. 15.0-15.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 10. | Neurodevelopmental retardation, as assessed clinically and with magnetoencephalography and electroencephalography, associated with perinatal dioxin exposure | G. W. ten Tusscher M. M. Leijs L. C. C. de Boer J. Legler K. Olie H. Spekreijse B. W. van Dijk T. Vulsma J. Briet A. Ilsen J. G. Koppe |
2014 |
SCIENCE OF THE TOTAL ENVIRONMENT (491.0), pp. 235.0-239.0 |
9 | 0 | 0 | 0 | 0 | 0 | 9 | |
| 11. | Changes in body mass index in long-term childhood cancer survivors | Hanneke M. van Santen Ronald B. Geskus Steven Raemaekers A. S. Paul van Trotsenburg Thomas Vulsma Helena J. H. van der Pal Hubert N. Caron Leontien C. M. Kremer |
2015 |
CANCER 23.0 (121.0), pp. 4197.0-4204.0 |
1 | 0 | 0 | 0 | 0 | 0 | 1 | |
| Title | Authors | Year | Journal title |
|---|
| ชื่อโครงการ | Authors | ประเภทโครงการ | ปีงบประมาณ | ทุนวิจับ |
|---|