Datasets
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Search results
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Additional file 1: of Disease progression in women with X-linked adrenoleukodystrophy is slow
Huffnagel, I. C. (Creator), Dijkgraaf, M. (Creator), Janssens, G. (Creator), van Weeghel, M. (Contributor), Van Geel, B. M. (Contributor), Poll-The, B. (Contributor), Kemp, S. (Creator), Engelen, M. (Creator) & Weeghel, M. (Creator), Figshare, 2019
DOI: 10.6084/m9.figshare.7693295.v1, https://springernature.figshare.com/articles/Additional_file_1_of_Disease_progression_in_women_with_X-linked_adrenoleukodystrophy_is_slow/7693295/1
Dataset
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MOESM4 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252091, https://springernature.figshare.com/articles/MOESM4_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252091
Dataset
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MOESM3 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252082, https://springernature.figshare.com/articles/MOESM3_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252082
Dataset
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Additional file 1: of Disease progression in women with X-linked adrenoleukodystrophy is slow
Huffnagel, I. C. (Creator), Dijkgraaf, M. (Creator), Janssens, G. (Creator), van Weeghel, M. (Contributor), Van Geel, B. M. (Contributor), Poll-The, B. (Contributor), Kemp, S. (Creator), Engelen, M. (Creator) & Weeghel, M. (Creator), Figshare, 2019
DOI: 10.6084/m9.figshare.7693295, https://springernature.figshare.com/articles/Additional_file_1_of_Disease_progression_in_women_with_X-linked_adrenoleukodystrophy_is_slow/7693295
Dataset
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MOESM2 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252073, https://springernature.figshare.com/articles/MOESM2_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252073
Dataset
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Additional file 2: of Disease progression in women with X-linked adrenoleukodystrophy is slow
Huffnagel, I. C. (Creator), Dijkgraaf, M. (Creator), Janssens, G. (Creator), van Weeghel, M. (Contributor), Van Geel, B. M. (Contributor), Poll-The, B. (Contributor), Kemp, S. (Creator), Engelen, M. (Creator) & Weeghel, M. (Creator), Figshare, 2019
DOI: 10.6084/m9.figshare.7693298.v1, https://springernature.figshare.com/articles/Additional_file_2_of_Disease_progression_in_women_with_X-linked_adrenoleukodystrophy_is_slow/7693298/1
Dataset
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MOESM3 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252082.v1, https://springernature.figshare.com/articles/MOESM3_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252082/1
Dataset
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MOESM4 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252091.v1, https://springernature.figshare.com/articles/MOESM4_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252091/1
Dataset
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MOESM5 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252100.v1, https://springernature.figshare.com/articles/MOESM5_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252100/1
Dataset
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Supplementary Material for: Low FT4 Concentrations around the Start of Recombinant Human Growth Hormone Treatment: Predictor of Congenital Structural Hypothalamic-Pituitary Abnormalities?
Van Iersel, L. (Creator), Van Santen, H. M. (Creator), Zwaveling-Soonawala, N. (Creator), Hokken-Koelega, A. C. S. (Contributor) & van Trotsenburg, A. (Contributor), Karger Publishers, 2018
DOI: 10.6084/m9.figshare.5798904, https://karger.figshare.com/articles/Supplementary_Material_for_Low_FT4_Concentrations_around_the_Start_of_Recombinant_Human_Growth_Hormone_Treatment_Predictor_of_Congenital_Structural_Hypothalamic-Pituitary_Abnormalities_/5798904
Dataset
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Supplementary Material for: Towards a Rational and Efficient Diagnostic Approach in Children Referred for Tall Stature and/or Accelerated Growth to the General Paediatrician
Lauffer, P. (Creator), Kamp, G. A. (Creator), Menke, L. (Creator), Wit, J. M. (Creator), Oostdijk, W. (Creator) & Wit, J. M. (Creator), Karger Publishers, 2019
DOI: 10.6084/m9.figshare.8863559.v1, https://karger.figshare.com/articles/Supplementary_Material_for_Towards_a_Rational_and_Efficient_Diagnostic_Approach_in_Children_Referred_for_Tall_Stature_and_or_Accelerated_Growth_to_the_General_Paediatrician/8863559/1
Dataset
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Supplementary Material for: Administration of Thyrotropin-Releasing Hormone in the Hypothalamic Paraventricular Nucleus of Male Rats Mimics the Metabolic Cold Defense Response
Zhang, Z. (Creator), Machado, F. (Creator), Zhao, L. (Creator), Heinen, C. (Creator), Foppen, E. (Creator), Ackermans, M. T. (Creator), Zhou, J. (Creator), Bisschop, P. (Creator), Boelen, A. (Creator), Fliers, E. (Creator), Kalsbeek, A. (Creator), Zhang, Z. (Creator) & Machado, F. (Creator), Karger Publishers, 2018
DOI: 10.6084/m9.figshare.7093580, https://karger.figshare.com/articles/Supplementary_Material_for_Administration_of_Thyrotropin-Releasing_Hormone_in_the_Hypothalamic_Paraventricular_Nucleus_of_Male_Rats_Mimics_the_Metabolic_Cold_Defense_Response/7093580
Dataset
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Additional file 7: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878920.v1, https://springernature.figshare.com/articles/Additional_file_7_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878920/1
Dataset
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Additional file 2: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878881, https://springernature.figshare.com/articles/Additional_file_2_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878881
Dataset
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Additional file 8: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878923.v1, https://springernature.figshare.com/articles/Additional_file_8_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878923/1
Dataset
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Additional file 8: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878923, https://springernature.figshare.com/articles/Additional_file_8_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878923
Dataset
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Additional file 10: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878860.v1, https://springernature.figshare.com/articles/Additional_file_10_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878860/1
Dataset
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S2 Data from Sustained effects of prior red light on pupil diameter and vigilance during subsequent darkness.
Van Der Meijden, W. P. (Contributor), Te Lindert, B. H. W. (Contributor), Ramauta, J. R. (Contributor), Wei, Y. (Contributor), Coppens, J. E. (Creator), Kamermans, M. (Creator), Cajochen, C. (Creator), Bourgin, P. (Creator), Van Someren, E. J. W. (Contributor), Lindert, B. H. W. T. (Creator) & Ramautar, J. R. (Creator), The Royal Society, 2018
DOI: 10.6084/m9.figshare.6743369, https://rs.figshare.com/articles/dataset/S2_Data_from_Sustained_effects_of_prior_red_light_on_pupil_diameter_and_vigilance_during_subsequent_darkness/6743369
Dataset
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S2 Data from Sustained effects of prior red light on pupil diameter and vigilance during subsequent darkness.
Van Der Meijden, W. P. (Contributor), Te Lindert, B. H. W. (Contributor), Ramauta, J. R. (Contributor), Wei, Y. (Contributor), Coppens, J. E. (Creator), Kamermans, M. (Creator), Cajochen, C. (Creator), Bourgin, P. (Creator), Van Someren, E. J. W. (Contributor), Lindert, B. H. W. T. (Creator) & Ramautar, J. R. (Creator), The Royal Society, 2018
DOI: 10.6084/m9.figshare.6743369.v2, https://rs.figshare.com/articles/dataset/S2_Data_from_Sustained_effects_of_prior_red_light_on_pupil_diameter_and_vigilance_during_subsequent_darkness/6743369/2
Dataset
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S1 Data from Sustained effects of prior red light on pupil diameter and vigilance during subsequent darkness
Van Der Meijden, W. P. (Contributor), Te Lindert, B. H. W. (Contributor), Ramauta, J. R. (Contributor), Wei, Y. (Contributor), Coppens, J. E. (Creator), Kamermans, M. (Creator), Cajochen, C. (Creator), Bourgin, P. (Creator), Van Someren, E. J. W. (Contributor), Lindert, B. H. W. T. (Creator) & Ramautar, J. R. (Creator), Figshare, 2018
DOI: 10.6084/m9.figshare.6833381, https://figshare.com/articles/S1_Data_from_Sustained_effects_of_prior_red_light_on_pupil_diameter_and_vigilance_during_subsequent_darkness/6833381
Dataset
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MOESM6 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252106, https://springernature.figshare.com/articles/MOESM6_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252106
Dataset
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MOESM1 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252070.v1, https://springernature.figshare.com/articles/MOESM1_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252070/1
Dataset
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MOESM1 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252070, https://springernature.figshare.com/articles/MOESM1_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252070
Dataset
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Data from: Idiopathic inflammatory myopathy: inter-rater variability in muscle biopsy reading
Olivier, P. A. (Creator), De Paepe, B. (Creator), Aronica, E. (Creator), Berfelo, F. (Creator), Colman, R. (Creator), Amato, A. (Creator), Dimitri, D. (Creator), Gallardo, E. (Creator), Gherardi, R. (Creator), Goebel, H. (Creator), Hilton-Jones, D. (Creator), Hofer, M. (Creator), Holton, J. (Creator), Schrøder, H. D. (Creator), Selcen, D. (Creator), Stenzel, W. (Creator), de Visser, M. (Contributor), De Bleecker, J. L. (Creator), Hofer, M. (Creator) & Selcen, D. (Creator), Dryad, 9 Sept 2019
DOI: 10.5061/dryad.s9p5c79, https://datadryad.org/stash/dataset/doi:10.5061/dryad.s9p5c79
Dataset
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Additional file 2: of Disease progression in women with X-linked adrenoleukodystrophy is slow
Huffnagel, I. C. (Creator), Dijkgraaf, M. (Creator), Janssens, G. (Creator), van Weeghel, M. (Contributor), Van Geel, B. M. (Contributor), Poll-The, B. (Contributor), Kemp, S. (Creator), Engelen, M. (Creator) & Weeghel, M. (Creator), Figshare, 2019
DOI: 10.6084/m9.figshare.7693298, https://springernature.figshare.com/articles/Additional_file_2_of_Disease_progression_in_women_with_X-linked_adrenoleukodystrophy_is_slow/7693298
Dataset