• 2720 Citations
  • 26 h-Index
19982018
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Fingerprint Dive into the research topics where Matthias Wolf is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 1 Similar Profiles
Mutation Medicine & Life Sciences
Genes Medicine & Life Sciences
Uromodulin Medicine & Life Sciences
Kidney Medicine & Life Sciences
Chromosomes Medicine & Life Sciences
Cystic Kidney Diseases Medicine & Life Sciences
Nephrotic Syndrome Medicine & Life Sciences
Haplotypes Medicine & Life Sciences

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Research Output 1998 2018

  • 2720 Citations
  • 26 h-Index
  • 45 Article
  • 1 Chapter
  • 1 Short survey

Mercury Intoxication as a Rare Cause of Membranous Nephropathy in a Child

Onwuzuligbo, O., Hendricks, A. R., Hassler, J., Domanski, K., Goto, C. & Wolf, M. T. F., Jan 1 2018, (Accepted/In press) In : American Journal of Kidney Diseases.

Research output: Contribution to journalArticle

Membranous Glomerulonephritis
Mercury
Nephrotic Syndrome
Phospholipase A2 Receptors
Thrombospondin 1
9 Citations (Scopus)

Single molecule real time sequencing in ADTKD-MUC1 allows complete assembly of the VNTR and exact positioning of causative mutations

Wenzel, A., Altmueller, J., Ekici, A. B., Popp, B., Stueber, K., Thiele, H., Pannes, A., Staubach, S., Salido, E., Nuernberg, P., Reinhardt, R., Reis, A., Rump, P., Hanisch, F. G., Wolf, M. T. F., Wiesener, M., Huettel, B. & Beck, B. B., Dec 1 2018, In : Scientific Reports. 8, 1, 4170.

Research output: Contribution to journalArticle

Mucin-1
Minisatellite Repeats
Kidney Diseases
Mutation
Dominant Genes
1 Citation (Scopus)

Uromodulin regulates renal magnesium homeostasis through the ion channel transient receptor potential melastatin 6 (TRPM6)

Nie, M., Bal, M. S., Liu, J., Yang, Z., Rivera, C., Wu, X. R., Hoenderop, J. G. J., Bindels, R. J. M., Marciano, D. K. & Wolf, M. T. F., Jan 1 2018, In : Journal of Biological Chemistry. 293, 42, p. 16488-16502 15 p.

Research output: Contribution to journalArticle

Uromodulin
Ion Channels
Magnesium
Homeostasis
Kidney
40 Citations (Scopus)

Mutations in KEOPS-complex genes cause nephritic syndrome with primary microcephaly

Braun, D. A., Rao, J., Mollet, G., Schapiro, D., Daugeron, M. C., Tan, W., Gribouval, O., Boyer, O., Revy, P., Jobst-Schwan, T., Schmidt, J. M., Lawson, J. A., Schanze, D., Ashraf, S., Ullmann, J. F. P., Hoogstraten, C. A., Boddaert, N., Collinet, B., Martin, G., Liger, D. & 82 others, Lovric, S., Furlano, M., Guerrera, I. C., Sanchez-Ferras, O., Hu, J. F., Boschat, A. C., Sanquer, S., Menten, B., Vergult, S., De Rocker, N., Airik, M., Hermle, T., Shril, S., Widmeier, E., Yung Gee, H., Choi, W. I., Sadowski, C. E., Pabst, W. L., Warejko, J. K., Daga, A., Basta, T., Matejas, V., Scharmann, K., Kienast, S. D., Behnam, B., Beeson, B., Begtrup, A., Bruce, M., Ch'Ng, G. S., Lin, S. P., Chang, J. H., Chen, C. H., Cho, M. T., Gaffney, P. M., Gipson, P. E., Hsu, C. H., Kari, J. A., Ke, Y. Y., Kiraly-Borri, C., Lai, W. M., Lemyre, E., Littlejohn, R. O., Masri, A., Moghtaderi, M., Nakamura, K., Ozaltin, F., Praet, M., Prasad, C., Prytula, A., Roeder, E. R., Rump, P., Schnur, R. E., Shiihara, T., Sinha, M. D., Soliman, N. A., Soulami, K., Sweetser, D. A., Tsai, W. H., Tsai, J. D., Topaloglu, R., Vester, U., Viskochil, D. H., Vatanavicharn, N., Waxler, J. L., Wierenga, K. J., Wolf, M. T. F., Wong, S. N., Leidel, S. A., Truglio, G., Dedon, P. C., Poduri, A., Mane, S., Lifton, R. P., Bouchard, M., Kannu, P., Chitayat, D., Magen, D., Callewaert, B., Van Tilbeurgh, H., Zenker, M., Antignac, C. & Hildebrandt, F., Oct 1 2017, In : Nature Genetics. 49, 10, p. 1529-1538 10 p.

Research output: Contribution to journalArticle

Microcephaly
Kidney
Mutation
Genes
Clustered Regularly Interspaced Short Palindromic Repeats

Omental Arteriopathy in Primary Atypical Hemolytic Uremic Syndrome

Ellington, N., Wolf, M., Kasten, J. & Rakheja, D., Sep 1 2017, In : International Journal of Surgical Pathology. 25, 6, p. 515-517 3 p.

Research output: Contribution to journalShort survey

Atypical Hemolytic Uremic Syndrome