Rik Westland

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Research activity per year

Keywords

R Medicine (General)
Pediatric Nephrology
Genetics
Transplantation

1 Active

ArtDECO: ArtDECO - = Aetiology of renal and urinary tract malformations determines Diagnostic Efficacy and Clinical Outcome
Westland, R.
1/12/2021 → 1/12/2026
Project: Research

25 Article
4 Review article
1 Comment/Letter to the editor
1 Phd-Thesis - Research and graduation internal

Environmental and parental risk factors for congenital solitary functioning kidney — a case–control study
SOFIA study group, Aug 2023, In: Pediatric Nephrology. 38, 8, p. 2631-2641 11 p.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access

1 Citation (Scopus)
Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies.
Westland, R., 25 Dec 2023, In: Genetics in medicine. 25, 12, 100983.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome
Barry, A., McNulty, M. T., Jia, X., Gupta, Y., Debiec, H., Luo, Y., Nagano, C., Horinouchi, T., Jung, S., Colucci, M., Ahram, D. F., Mitrotti, A., Sinha, A., Teeninga, N., Jin, G., Shril, S., Caridi, G., Bodria, M., Lim, T. Y., Westland, R., & 50 othersZanoni, F., Marasa, M., Turudic, D., Giordano, M., Gesualdo, L., Magistroni, R., Pisani, I., Fiaccadori, E., Reiterova, J., Maringhini, S., Morello, W., Montini, G., Weng, P. L., Scolari, F., Saraga, M., Tasic, V., Santoro, D., van Wijk, J. A. E., Milošević, D., Kawai, Y., Kiryluk, K., Pollak, M. R., Gharavi, A., Lin, F., Simœs e Silva, A. C., Loos, R. J. F., Kenny, E. E., Schreuder, M. F., Zurowska, A., Dossier, C., Ariceta, G., Drozynska-Duklas, M., Hogan, J., Jankauskiene, A., Hildebrandt, F., Prikhodina, L., Song, K., Bagga, A., Cheong, H., Ghiggeri, G. M., Vachvanichsanong, P., Nozu, K., Lee, D., Vivarelli, M., Raychaudhuri, S., Tokunaga, K., Sanna-Cherchi, S., Ronco, P., Iijima, K. & Sampson, M. G., 1 Dec 2023, In: Nature communications. 14, 1, 2481.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access

6 Citations (Scopus)
Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis: Implications for Genetic Diagnosis
Westland, R. & van Wijk, J. A. E., 1 Jun 2023, In: Journal of the American Society of Nephrology. 34, 6, p. 1105-1119 15 p.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access

1 Citation (Scopus)
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
Gupta, Y., Friedman, D. J., McNulty, M. T., Khan, A., Lane, B., Wang, C., Ke, J., Jin, G., Wooden, B., Knob, A. L., Lim, T. Y., Appel, G. B., Huggins, K., Liu, L., Mitrotti, A., Stangl, M. C., Bomback, A., Westland, R., Bodria, M., Marasa, M., & 60 othersShang, N., Cohen, D. J., Crew, R. J., Morello, W., Canetta, P., Radhakrishnan, J., Martino, J., Liu, Q., Chung, W. K., Espinoza, A., Luo, Y., Wei, W-Q., Feng, Q., Weng, C., Fang, Y., Kullo, I. J., Naderian, M., Limdi, N., Irvin, M. R., Tiwari, H., Mohan, S., Rao, M., Dube, G. K., Chaudhary, N. S., Gutiérrez, O. M., Judd, S. E., Cushman, M., Lange, L. A., Lange, E. M., Bivona, D. L., Verbitsky, M., Winkler, C. A., Kopp, J. B., Santoriello, D., Batal, I., Pinheiro, S. R. V. B., Oliveira, E. A., Simoes e Silva, A. C., Pisani, I., Fiaccadori, E., Lin, F., Gesualdo, L., Amoroso, A., Ghiggeri, G. M., D’Agati, V. D., Magistroni, R., Kenny, E. E., Loos, R. J. F., Montini, G., Hildebrandt, F., Paul, D. S., Petrovski, S., Goldstein, D. B., Kretzler, M., Gbadegesin, R., Gharavi, A. G., Kiryluk, K., Sampson, M. G., Pollak, M. R. & Sanna-Cherchi, S., 1 Dec 2023, In: Nature communications. 14, 1, 7836.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access

2 Citations (Scopus)

Rik Westland

Personal profile

Keywords

Collaborations and top research areas from the last five years

Dive into details

ArtDECO: ArtDECO - = Aetiology of renal and urinary tract malformations determines Diagnostic Efficacy and Clinical Outcome

Environmental and parental risk factors for congenital solitary functioning kidney — a case–control study

Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies.

Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis: Implications for Genetic Diagnosis

Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease

Rik Westland

Personal profile

Keywords

Collaborations and top research areas from the last five years

Projects

ArtDECO: ArtDECO - = Aetiology of renal and urinary tract malformations determines Diagnostic Efficacy and Clinical Outcome

Research output

Environmental and parental risk factors for congenital solitary functioning kidney — a case–control study

Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies.

Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis: Implications for Genetic Diagnosis

Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease