Research ExplorerScientific StaffKerstin Kutsche Publications

Prof. Dr. ID: 40416

Kerstin Kutsche

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  1. SCORING: Contribution to collected editions/anthologies › Research › Peer-reviewed

  2. EBF3 Neurodevelopmental Disorder

    Narayanan, D. L., Kutsche, K. & Girisha, K. M., 06.05.2021, GeneReviews®. 1 ed. Seattle: University of Washington, Seattle, Vol. 1993-2021. p. 1-9 9 p. (GeneReviews® [Internet]).

    Research output: SCORING: Contribution to book/anthology › SCORING: Contribution to collected editions/anthologies › Research › peer-review

  3. SCORING: Contribution to collected editions/anthologies › Transfer › Not peer-reviewed

  4. Vererbung und Genetische Tests

    Kutsche, K., 2016, Das Marfan-Syndrom. M. H. D. E. V. (ed.). 1 ed. Springer, p. 47-56 10 p. 11

    Research output: SCORING: Contribution to book/anthology › SCORING: Contribution to collected editions/anthologies › Transfer

  5. SCORING: Journal article › Research › Peer-reviewed

  6. A 1-bp duplication in TGFB2 in three family members with a syndromic form of thoracic aortic aneurysm

    Leutermann, R., Sheikhzadeh, S., Brockstädt, L., Rybczynski, M., van Rahden, V., Kutsche, K., Kodolitsch, Y. & Rosenberger, G., 06.11.2013, In: EUR J HUM GENET. 22, p. 944-948

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  7. Activating Mutations in PAK1, Encoding p21-Activated Kinase 1, Cause a Neurodevelopmental Disorder

    Harms, F. L., Kloth, K., Bley, A., Denecke, J., Santer, R., Lessel, D., Hempel, M. & Kutsche, K., 04.10.2018, In: AM J HUM GENET. 103, 4, p. 579-591 13 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  8. Acute Liver Failure Meets SOPH Syndrome: A Case Report on an Intermediate Phenotype

    Kortüm, F., Marquardt, I., Alawi, M., Korenke, G. C., Spranger, S., Meinecke, P. & Kutsche, K., 01.2017, In: PEDIATRICS. 139, 1, p. pii: e20160550

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  9. A deep intronic variant in DNM1 in a patient with developmental and epileptic encephalopathy creates a splice acceptor site and affects only transcript variants including exon 10a

    Harms, F. L., Weiss, D., Lisfeld, J., Alawi, M. & Kutsche, K., 07.2023, In: NEUROGENETICS. 24, 3, p. 171-180 10 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  10. A homozygous hypomorphic BNIP1 variant causes an increase in autophagosomes and reduced autophagic flux and results in a spondylo-epiphyseal dysplasia

    Holling, T., Bhavani, G. S., von Elsner, L., Shah, H., Kausthubham, N., Bhattacharyya, S. S., Shukla, A., Mortier, G. R., Schinke, T., Danyukova, T., Pohl, S., Kutsche, K. & Girisha, K. M., 05.2022, In: HUM MUTAT. 43, 5, p. 625-642 18 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  11. A homozygous ATAD1 mutation impairs postsynaptic AMPA receptor trafficking and causes a lethal encephalopathy

    Piard, J., Umanah, G. K. E., Harms, F. L., Abalde-Atristain, L., Amram, D., Chang, M., Chen, R., Alawi, M., Salpietro, V., Rees, M. I., Chung, S-K., Houlden, H., Verloes, A., Dawson, T. M., Dawson, V. L., Van Maldergem, L. & Kutsche, K., 01.03.2018, In: BRAIN. 141, 3, p. 651-661 11 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  12. A homozygous missense variant in CACNB4 encoding the auxiliary calcium channel beta4 subunit causes a severe neurodevelopmental disorder and impairs channel and non-channel functions

    Coste de Bagneaux, P., von Elsner, L., Bierhals, T., Campiglio, M., Johannsen, J., Obermair, G. J., Hempel, M., Flucher, B. E. & Kutsche, K., 03.2020, In: PLOS GENET. 16, 3, p. e1008625

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  13. AlphaPIX and betaPIX and their role in focal adhesion formation

    Rosenberger, G. & Kutsche, K., 2006, In: EUR J CELL BIOL. 85, 3-4, p. 265-274 10 p., 3-4.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  14. AlphaPIX Rho GTPase guanine nucleotide exchange factor regulates lymphocyte functions and antigen receptor signaling.

    Missy, K., Hu, B., Schilling, K., Harenberg, A., Sakk, V., Kuchenbecker, K., Kutsche, K. & Fischer, K-D., 2008, In: MOL CELL BIOL. 28, 11, p. 3776-3789 11.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  15. Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasia.

    Dalal, A., Bhavani, G., Lakshmi, S., Bierhals, T., Bierhals, T., Nandineni, M. R., Danda, S., Danda, D., Shah, H., Vijayan, S., Gowrishankar, K., Phadke, S. R., Bidchol, A. M., Rao, A. P., Kutsche, K., Kutsche, K. & Girisha, K. M., 2012, In: AM J MED GENET A. 158A, 11, p. 2820-2828 11.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  16. An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome

    Abdollahpour, H., Alawi, M., Kortüm, F., Beckstette, M., Seemanova, E., Komárek, V., Rosenberger, G. & Kutsche, K., 2015, In: EUR J HUM GENET. 23, 2, p. 256-259

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  17. A novel multiple joint dislocation syndrome associated with a homozygous nonsense variant in the EXOC6B gene

    Girisha, K. M., Kortüm, F., Shah, H., Alawi, M., Dalal, A., Bhavani, G. S. & Kutsche, K., 01.08.2016, In: EUR J HUM GENET. 24, 8, p. 1206-10

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  18. A Recurrent Gain-of-Function Mutation in CLCN6, Encoding the ClC-6 Cl-/H+-Exchanger, Causes Early-Onset Neurodegeneration

    Polovitskaya, M. M., Barbini, C., Martinelli, D., Harms, F. L., Cole, F. S., Calligari, P., Bocchinfuso, G., Stella, L., Ciolfi, A., Niceta, M., Rizza, T., Shinawi, M., Sisco, K., Johannsen, J., Denecke, J., Carrozzo, R., Wegner, D. J., Kutsche, K., Tartaglia, M. & Jentsch, T. J., 03.12.2020, In: AM J HUM GENET. 107, 6, p. 1062-1077 16 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  19. A restricted spectrum of NRAS mutations causes Noonan syndrome.

    Cirstea, I. C., Kutsche, K., Dvorsky, R., Gremer, L., Carta, C., Horn, D., Roberts, A. E., Lepri, F., Merbitz-Zahradnik, T., König, R., Kratz, C. P., Pantaleoni, F., Dentici, M. L., Joshi, V. A., Kucherlapati, R. S., Mazzanti, L., Mundlos, S., Patton, M. A., Silengo, M. C., Rossi, C., Zampino, G., Digilio, C., Stuppia, L., Seemanova, E., Pennacchio, L. A., Gelb, B. D., Dallapiccola, B., Wittinghofer, A., Ahmadian, M. R., Tartaglia, M. & Zenker, M., 2010, In: NAT GENET. 42, 1, p. 27-29 1.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  20. A severe form of the X-linked microphthalmia with linear skin defects syndrome in a female newborn.

    Steichen-Gersdorf, E., Griesmaier, E., Pientka, F. K., Kotzot, D. & Kutsche, K., 2010, In: CLIN DYSMORPHOL. 19, 2, p. 82-84 2.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  21. A syndrome of facial dysmorphism, cubital pterygium, short distal phalanges, swan neck deformity of fingers, and scoliosis

    Girisha, K. M., Abdollahpour, H., Shah, H., Bhavani, G. S., Graham, J. M., Boggula, V. R., Phadke, S. R. & Kutsche, K., 01.04.2014, In: AM J MED GENET A. 164A, 4, p. 1035-40 6 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  22. A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation.

    Martínez-Garay, I., Tomás, M., Oltra, S., Ramser, J., Moltó, M. D., Prieto, F., Meindl, A., Kutsche, K. & Martínez, F., 2007, In: EUR J HUM GENET. 15, 1, p. 29-34 1.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  23. Autosomal dominantly inherited myopathy likely caused by the TNNT1 variant p.(Asp65Ala)

    Holling, T., Lisfeld, J., Johannsen, J., Matschke, J., Song, F., Altmeppen, H. C. & Kutsche, K., 09.2022, In: HUM MUTAT. 43, 9, p. 1224-1233 10 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  24. Autosomal dominant Robinow syndrome associated with a novel DVL3 splice mutation

    Danyel, M., Kortüm, F., Dathe, K., Kutsche, K. & Horn, D., 04.2018, In: AM J MED GENET A. 176, 4, p. 992-996 5 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  25. Biallelic CACNA2D1 loss-of-function variants cause early-onset developmental epileptic encephalopathy

    Dahimene, S., von Elsner, L., Holling, T., Mattas, L. S., Pickard, J., Lessel, D., Pilch, K. S., Kadurin, I., Pratt, W. S., Zhulin, I. B., Dai, H., Hempel, M., Ruzhnikov, M. R. Z., Kutsche, K. & Dolphin, A. C., 27.08.2022, In: BRAIN. 145, 8, p. 2721-2729 9 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  26. Biallelic FRA10AC1 variants cause a neurodevelopmental disorder with growth retardation

    von Elsner, L., Chai, G., Schneeberger, P. E., Harms, F. L., Casar, C., Qi, M., Alawi, M., Abdel-Salam, G. M. H., Zaki, M. S., Arndt, F., Yang, X., Stanley, V., Hempel, M., Gleeson, J. G. & Kutsche, K., 24.05.2022, In: BRAIN. 145, 4, p. 1551-1563 13 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  27. Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder

    Schneeberger, P. E., Kortüm, F., Korenke, G. C., Alawi, M., Santer, R., Woidy, M., Buhas, D., Fox, S., Juusola, J., Alfadhel, M., Webb, B. D., Coci, E. G., Abou Jamra, R., Siekmeyer, M., Biskup, S., Heller, C., Maier, E. M., Javaher-Haghighi, P., Bedeschi, M. F., Ajmone, P. F., Iascone, M., Peeters, H., Ballon, K., Jaeken, J., Rodríguez Alonso, A., Palomares-Bralo, M., Santos-Simarro, F., Meuwissen, M. E. C., Beysen, D., Kooy, R. F., Houlden, H., Murphy, D., Doosti, M., Karimiani, E. G., Mojarrad, M., Maroofian, R., Noskova, L., Kmoch, S., Honzik, T., Cope, H., Sanchez-Valle, A., Undiagnosed Diseases Network, Gelb, B. D., Kurth, I., Hempel, M. & Kutsche, K., 01.08.2020, In: BRAIN. 143, 8, p. 2437-2453 17 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  28. Biallelic loss-of-function variants in TBC1D2B cause a neurodevelopmental disorder with seizures and gingival overgrowth

    Harms, F. L., Parthasarathy, P., Zorndt, D., Alawi, M., Fuchs, S., Halliday, B. J., McKeown, C., Sampaio, H., Radhakrishnan, N., Radhakrishnan, S. K., Gorce, M., Navet, B., Ziegler, A., Sachdev, R., Robertson, S. P., Nampoothiri, S. & Kutsche, K., 09.2020, In: HUM MUTAT. 41, 9, p. 1645-1661 17 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  29. Bi-allelic Pathogenic Variants in HS2ST1 Cause a Syndrome Characterized by Developmental Delay and Corpus Callosum, Skeletal, and Renal Abnormalities

    Schneeberger, P. E., von Elsner, L., Barker, E. L., Meinecke, P., Marquardt, I., Alawi, M., Steindl, K., Joset, P., Rauch, A., Zwijnenburg, P. J. G., Weiss, M. M., Merry, C. L. R. & Kutsche, K., 03.12.2020, In: AM J HUM GENET. 107, 6, p. 1044-1061 18 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  30. Bi-allelic variants in IPO8 cause a connective tissue disorder associated with cardiovascular defects, skeletal abnormalities, and immune dysregulation

    Ziegler, A., Duclaux-Loras, R., Revenu, C., Charbit-Henrion, F., Begue, B., Duroure, K., Grimaud, L., Guihot, A. L., Desquiret-Dumas, V., Zarhrate, M., Cagnard, N., Mas, E., Breton, A., Edouard, T., Billon, C., Frank, M., Colin, E., Lenaers, G., Henrion, D., Lyonnet, S., Faivre, L., Alembik, Y., Philippe, A., Moulin, B., Reinstein, E., Tzur, S., Attali, R., McGillivray, G., White, S. M., Gallacher, L., Kutsche, K., Schneeberger, P., Girisha, K. M., Nayak, S. S., Pais, L., Maroofian, R., Rad, A., Vona, B., Karimiani, E. G., Lekszas, C., Haaf, T., Martin, L., Ruemmele, F., Bonneau, D., Cerf-Bensussan, N., Del Bene, F. & Parlato, M., 03.06.2021, In: AM J HUM GENET. 108, 6, p. 1126-1137 12 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  31. Biallelic variants in SMAD6 are associated with a complex cardiovascular phenotype

    Kloth, K., Bierhals, T., Johannsen, J., Harms, F. L., Juusola, J., Johnson, M. C., Grange, D. K. & Kutsche, K., 06.2019, In: HUM GENET. 138, 6, p. 625-634 10 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  32. Biallelic variants in VPS50 cause a neurodevelopmental disorder with neonatal cholestasis

    Schneeberger, P. E., Nampoothiri, S., Holling, T., Yesodharan, D., Alawi, M., Knisely, A. S., Müller, T., Plecko, B., Janecke, A. R. & Kutsche, K., 26.05.2021, In: BRAIN. 2021, awab206

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  33. Branchio-otic syndrome caused by a genomic rearrangement: clinical findings and molecular cytogenetic studies in a patient with a pericentric inversion of chromosome 8

    Schmidt, T., Bierhals, T., Kortüm, F., Bartels, I., Liehr, T., Burfeind, P., Shoukier, M., Frank, V., Bergmann, C. & Kutsche, K., 01.01.2014, In: CYTOGENET GENOME RES. 142, 1, p. 1-6 6 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  34. Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes

    Kratz, C. P., Franke, L., Peters, H., Kohlschmidt, N., Kazmierczak, B., Finckh, U., Bier, A., Eichhorn, B., Blank, C., Kraus, C., Kohlhase, J., Pauli, S., Wildhardt, G., Kutsche, K., Auber, B., Christmann, A., Bachmann, N., Mitter, D., Cremer, F. W., Mayer, K., Daumer-Haas, C., Nevinny-Stickel-Hinzpeter, C., Oeffner, F., Schlüter, G., Gencik, M., Überlacker, B., Lissewski, C., Schanze, I., Greene, M. H., Spix, C. & Zenker, M., 14.04.2015, In: BRIT J CANCER. 112, 8, p. 1392-7 6 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  35. Candidate loci for Zimmermann-Laband syndrome at 3p14.3.

    Hyung-Goo, K., Higgins Anne, W., Herrick Steven, R., Kishikawa, S., Nicholson, L., Kutsche, K., Ligon Azra, H., Harris David, J., Macdonald Marcy, E., Bruns Gail, A. P., Morton Cynthia, C., Quade Bradley, J. & Gusella James, F., 2007, In: AM J MED GENET A. 143, 2, p. 107-111 2.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  36. Cantú syndrome versus Zimmermann-Laband syndrome: Report of nine individuals with ABCC9 variants

    Kortüm, F., Niceta, M., Magliozzi, M., Kubat, K. D., Robertson, S. P., Moresco, A., Dentici, M. L., Baban, A., Leoni, C., Onesimo, R., Obregon, M. G., Digilio, M. C., Zampino, G., Novelli, A., Tartaglia, M. & Kutsche, K., 09.2020, In: EUR J MED GENET. 63, 9, p. 103996

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  37. Cardiofacioneurodevelopmental syndrome: Report of a novel patient and expansion of the phenotype

    Abdalla, E., Alawi, M., Meinecke, P., Kutsche, K. & Harms, F. L., 08.2022, In: AM J MED GENET A. 188, 8, p. 2448-2453 6 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  38. Case-matched Comparison of Cardiovascular Outcome in Loeys-Dietz Syndrome versus Marfan Syndrome

    Mühlstädt, K., De Backer, J., von Kodolitsch, Y., Kutsche, K., Muiño Mosquera, L., Brickwedel, J., Girdauskas, E., Mir, T. S., Mahlmann, A., Tsilimparis, N., Staebler, A., Schoof, L., Seidel, H., Berger, J., Bernhardt, A. M., Blankenberg, S., Kölbel, T., Detter, C., Szöcs, K. & Kaemmerer, H., 29.11.2019, In: J CLIN MED. 8, 12

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  39. CASK-Related Disorders

    Moog, U., Uyanik, G. & Kutsche, K., 26.11.2013, In: GeneReviews®.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  40. Clinical and genetic diagnosis of Marfan syndrome in childhood are Equal- FBN1 mutation should not influence handling of pediatric patients with confirmed Marfansyndrome

    Stark, V., Arndt, F., Harring, G., Keyser, B., von Kodolitsch, Y., Kozlik-Feldmann, R., Kutsche, K., Müller, G., Rybczynski, M. & Mir, T., 12.01.2016, In: J Integr Cardiol.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  41. Clinical and genetic spectrum of AMPD2-related pontocerebellar hypoplasia type 9

    Kortüm, F., Jamra, R. A., Alawi, M., Berry, S. A., Borck, G., Helbig, K. L., Tang, S., Huhle, D., Korenke, G. C., Hebbar, M., Shukla, A., Girisha, K. M., Steinlin, M., Waldmeier-Wilhelm, S., Montomoli, M., Guerrini, R., Lemke, J. R. & Kutsche, K., 05.2018, In: EUR J HUM GENET. 26, 5, p. 695-708 14 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  42. Clinically Relevant KCNQ1 Variants Causing KCNQ1-KCNE2 Gain-of-Function Affect the Ca2+ Sensitivity of the Channel

    Bauer, C. K., Holling, T., Horn, D., Laço, M. N., Abdalla, E., Omar, O. M., Alawi, M. & Kutsche, K., 26.08.2022, In: INT J MOL SCI. 23, 17, 9690.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  43. Clinically relevant variants in a large cohort of Indian patients with Marfan syndrome and related disorders identified by next-generation sequencing

    Nayak, S. S., Schneeberger, P. E., Patil, S. J., Arun, K. M., Suresh, P. V., Kiran, V. S., Siddaiah, S., Maiya, S., Venkatachalagupta, S. K., Kausthubham, N., Kortüm, F., Rau, I., Wey-Fabrizius, A., Van Den Heuvel, L., Meester, J., Van Laer, L., Shukla, A., Loeys, B., Girisha, K. M. & Kutsche, K., 12.01.2021, In: SCI REP-UK. 11, 1, 764.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  44. Clinical spectrum of females with HCCS Mutation: from no clinical signs to a neonatal lethal form of the microphthalmia with linear skin defects (MLS) syndrome

    van Rahden, V. A., Rau, I., Fuchs, S., Kosyna, F. K., de Almeida, H. L., Fryssira, H., Isidor, B., Jauch, A., Joubert, M., Lachmeijer, A. M. A., Zweier, C., Moog, U. & Kutsche, K., 01.01.2014, In: ORPHANET J RARE DIS. 9, 1, p. 53

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  45. Comprehensive analysis of dural ectasia in 150 patients with a causative FBN1 mutation

    Sheikhzadeh, S., Sondermann, C., Rybczynski, M., Habermann, C. R., Brockstädt, L., Keyser, B., Kaemmerer, H., Mir, T., Staebler, A., Robinson, P. N., Kutsche, K., Berger, J., Blankenberg, S. & Kodolitsch, Y., 2014, In: CLIN GENET. 86, 3, p. 238-245

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  46. Costello syndrome with severe cutis laxa and mosaic HRAS G12S mutation

    Girisha, K. M., Lewis, L. E., Phadke, S. R. & Kutsche, K., 01.11.2010, In: AM J MED GENET A. 152A, 11, p. 2861-4 4 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  47. Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy

    Syrbe, S., Harms, F. L., Parrini, E., Montomoli, M., Mütze, U., Helbig, K. L., Polster, T., Albrecht, B., Bernbeck, U., van Binsbergen, E., Biskup, S., Burglen, L., Denecke, J., Heron, B., Heyne, H. O., Hoffmann, G. F., Hornemann, F., Matsushige, T., Matsuura, R., Kato, M., Korenke, G. C., Kuechler, A., Lämmer, C., Merkenschlager, A., Mignot, C., Ruf, S., Nakashima, M., Saitsu, H., Stamberger, H., Pisano, T., Tohyama, J., Weckhuysen, S., Werckx, W., Wickert, J., Mari, F., Verbeek, N. E., Møller, R. S., Koeleman, B., Matsumoto, N., Dobyns, W. B., Battaglia, D., Lemke, J. R., Kutsche, K. & Guerrini, R., 01.09.2017, In: BRAIN. 140, 9, p. 2322-2336 15 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  48. de novo PHF5A variants are associated with craniofacial abnormalities, developmental delay, and hypospadias

    Harms, F. L., Dingemans, A. J. M., Hempel, M., Pfundt, R., Bierhals, T., Casar, C., Müller, C., Niermeijer, J-M. F., Fischer, J., Jahn, A., Hübner, C., Majore, S., Agolini, E., Novelli, A., van der Smagt, J., Ernst, R., van Binsbergen, E., Mancini, G. M. S., van Slegtenhorst, M., Barakat, T. S., Wakeling, E. L., Kamath, A., Downie, L., Pais, L., White, S. M., de Vries, B. B. A. & Kutsche, K., 10.2023, In: GENET MED. 25, 10, p. 100927

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  49. Dermatoscopic aspects of the microphthalmia with linear skin defects (MLS) syndrome

    de Almeida, H. L., Rossi, G., de Abreu, L. B., Bergamaschi, C., da Silva, A. B. & Kutsche, K., 2014, In: AN BRAS DERMATOL. 89, 1, p. 180-1 2 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  50. Disruption of neurexin 1 associated with autism spectrum disorder.

    Kim, H-G., Kishikawa, S., Higgins, A. W., Seong, I-S., Donovan Diana, J., Shen, Y., Lally, E., Weiss, L. A., Najm, J., Kutsche, K., Descartes, M., Holt, L., Braddock, S., Troxell, R., Kaplan, L., Volkmar, F., Klin, A., Tsatsanis, K., Harris, D. J., Noens, I., Pauls, D. L., Daly, M. J., MacDonald, M. E., Morton, C. C., Quade Bradley, J. & Gusella, J. F., 2008, In: AM J HUM GENET. 82, 1, p. 199-207 1.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  51. Duplication of Glu37 in the switch I region of HRAS impairs effector/GAP binding and underlies Costello syndrome by promoting enhanced growth factor-dependent MAPK and AKT activation.

    Gremer, L., Alessandro, D. L., Merbitz-Zahradnik, T., Dallapiccola, B., Morlot, S., Tartaglia, M., Kutsche, K., Ahmadian, M. R. & Rosenberger, G., 2009, In: HUM MOL GENET.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  52. Dural ectasia in Loeys-Dietz Syndrome: comprehensive study of 30 patients with a TGFBR1 or TGFBR2 mutation

    Sheikhzadeh, S., Brockstädt, L., Habermann, C. R., Sondermann, C., Bannas, P., Mir, T. S., Staebler, A., Seidel, H., Keyser, B., Arslan-Kirchner, M., Kutsche, K., Berger, J., Blankenberg, S. & Kodolitsch, Y., 01.12.2014, In: CLIN GENET. 86, 6, p. 545-551 7 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  53. Dysfunction of SHANK2 and CHRNA7 in a patient with intellectual disability and language impairment supports genetic epistasis of the two loci

    Chilian, B., Abdollahpour, H., Bierhals, T., Haltrich, I., Fekete, G., Nagel, I., Rosenberger, G. & Kutsche, K., 01.12.2013, In: CLIN GENET. 84, 6, p. 560-5 6 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

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