Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.

Schmidt A, Danyel M, Grundmann K, Brunet T, Klinkhammer H, Hsieh TC, Engels H, Peters S, Knaus A, Moosa S, Averdunk L, Boschann F, Sczakiel HL, Schwartzmann S, Mensah MA, Pantel JT, Holtgrewe M, Bösch A, Weiß C, Weinhold N, Suter AA, Stoltenburg C, Neugebauer J, Kallinich T, Kaindl AM, Holzhauer S, Bührer C, Bufler P, Kornak U, Ott CE, Schülke M, Nguyen HHP, Hoffjan S, Grasemann C, Rothoeft T, Brinkmann F, Matar N, Sivalingam S, Perne C, Mangold E, Kreiss M, Cremer K, Betz RC, Mücke M, Grigull L, Klockgether T, Spier I, Heimbach A, Bender T, Brand F, Stieber C, Morawiec AM, Karakostas P, Schäfer VS, Bernsen S, Weydt P, Castro-Gomez S, Aziz A, Grobe-Einsler M, Kimmich O, Kobeleva X, Önder D, Lesmann H, Kumar S, Tacik P, Bhasin MA, Incardona P, Lee-Kirsch MA, Berner R, Schuetz C, Körholz J, Kretschmer T, Di Donato N, Schröck E, Heinen A, Reuner U, Hanßke AM, Kaiser FJ, Manka E, Munteanu M, Kuechler A, Cordula K, Hirtz R, Schlapakow E, Schlein C, Lisfeld J, Kubisch C, Herget T, Hempel M, Weiler-Normann C, Ullrich K, Schramm C, Rudolph C, Rillig F, Groffmann M, Muntau A, Tibelius A, Schwaibold EMC, Schaaf CP, Zawada M, Kaufmann L, Hinderhofer K, Okun PM, Kotzaeridou U, Hoffmann GF, Choukair D, Bettendorf M, Spielmann M, Ripke A, Pauly M, Münchau A, Lohmann K, Hüning I, Hanker B, Bäumer T, Herzog R, Hellenbroich Y, Westphal DS, Strom T, Kovacs R, Riedhammer KM, Mayerhanser K, Graf E, Brugger M, Hoefele J, Oexle K, Mirza-Schreiber N, Berutti R, Schatz U, Krenn M, Makowski C, Weigand H, Schröder S, Rohlfs M, Vill K, Hauck F, Borggraefe I, Müller-Felber W, Kurth I, Elbracht M, Knopp C, Begemann M, Kraft F, Lemke JR, Hentschel J, Platzer K, Strehlow V, Abou Jamra R, Kehrer M, Demidov G, Beck-Wödl S, Graessner H, Sturm M, Zeltner L, Schöls LJ, Magg J, Bevot A, Kehrer C, Kaiser N, Turro E, Horn D, Grüters-Kieslich A, Klein C, Mundlos S, Nöthen M, Riess O, Meitinger T, Krude H, Krawitz PM, Haack T, Ehmke N, Wagner M

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DOI: 10.1038/s41588-025-02271-6
Published: 2025 Jul
Container: Nature genetics
Publisher: Not recorded
Open access: yes

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BibTeX

@article{allodium:10.1038/s41588-025-02271-6,
  title = {Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.},
  author = {Schmidt A and Danyel M and Grundmann K and Brunet T and Klinkhammer H and Hsieh TC and Engels H and Peters S and Knaus A and Moosa S and Averdunk L and Boschann F and Sczakiel HL and Schwartzmann S and Mensah MA and Pantel JT and Holtgrewe M and Bösch A and Weiß C and Weinhold N and Suter AA and Stoltenburg C and Neugebauer J and Kallinich T and Kaindl AM and Holzhauer S and Bührer C and Bufler P and Kornak U and Ott CE and Schülke M and Nguyen HHP and Hoffjan S and Grasemann C and Rothoeft T and Brinkmann F and Matar N and Sivalingam S and Perne C and Mangold E and Kreiss M and Cremer K and Betz RC and Mücke M and Grigull L and Klockgether T and Spier I and Heimbach A and Bender T and Brand F and Stieber C and Morawiec AM and Karakostas P and Schäfer VS and Bernsen S and Weydt P and Castro-Gomez S and Aziz A and Grobe-Einsler M and Kimmich O and Kobeleva X and Önder D and Lesmann H and Kumar S and Tacik P and Bhasin MA and Incardona P and Lee-Kirsch MA and Berner R and Schuetz C and Körholz J and Kretschmer T and Di Donato N and Schröck E and Heinen A and Reuner U and Hanßke AM and Kaiser FJ and Manka E and Munteanu M and Kuechler A and Cordula K and Hirtz R and Schlapakow E and Schlein C and Lisfeld J and Kubisch C and Herget T and Hempel M and Weiler-Normann C and Ullrich K and Schramm C and Rudolph C and Rillig F and Groffmann M and Muntau A and Tibelius A and Schwaibold EMC and Schaaf CP and Zawada M and Kaufmann L and Hinderhofer K and Okun PM and Kotzaeridou U and Hoffmann GF and Choukair D and Bettendorf M and Spielmann M and Ripke A and Pauly M and Münchau A and Lohmann K and Hüning I and Hanker B and Bäumer T and Herzog R and Hellenbroich Y and Westphal DS and Strom T and Kovacs R and Riedhammer KM and Mayerhanser K and Graf E and Brugger M and Hoefele J and Oexle K and Mirza-Schreiber N and Berutti R and Schatz U and Krenn M and Makowski C and Weigand H and Schröder S and Rohlfs M and Vill K and Hauck F and Borggraefe I and Müller-Felber W and Kurth I and Elbracht M and Knopp C and Begemann M and Kraft F and Lemke JR and Hentschel J and Platzer K and Strehlow V and Abou Jamra R and Kehrer M and Demidov G and Beck-Wödl S and Graessner H and Sturm M and Zeltner L and Schöls LJ and Magg J and Bevot A and Kehrer C and Kaiser N and Turro E and Horn D and Grüters-Kieslich A and Klein C and Mundlos S and Nöthen M and Riess O and Meitinger T and Krude H and Krawitz PM and Haack T and Ehmke N and Wagner M},
  year = {2025},
  journal = {Nature genetics},
  doi = {10.1038/s41588-025-02271-6},
  url = {https://doi.org/10.1038/s41588-025-02271-6}
}

RIS

TY  - JOUR
TI  - Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.
AU  - Schmidt A
AU  - Danyel M
AU  - Grundmann K
AU  - Brunet T
AU  - Klinkhammer H
AU  - Hsieh TC
AU  - Engels H
AU  - Peters S
AU  - Knaus A
AU  - Moosa S
AU  - Averdunk L
AU  - Boschann F
AU  - Sczakiel HL
AU  - Schwartzmann S
AU  - Mensah MA
AU  - Pantel JT
AU  - Holtgrewe M
AU  - Bösch A
AU  - Weiß C
AU  - Weinhold N
AU  - Suter AA
AU  - Stoltenburg C
AU  - Neugebauer J
AU  - Kallinich T
AU  - Kaindl AM
AU  - Holzhauer S
AU  - Bührer C
AU  - Bufler P
AU  - Kornak U
AU  - Ott CE
AU  - Schülke M
AU  - Nguyen HHP
AU  - Hoffjan S
AU  - Grasemann C
AU  - Rothoeft T
AU  - Brinkmann F
AU  - Matar N
AU  - Sivalingam S
AU  - Perne C
AU  - Mangold E
AU  - Kreiss M
AU  - Cremer K
AU  - Betz RC
AU  - Mücke M
AU  - Grigull L
AU  - Klockgether T
AU  - Spier I
AU  - Heimbach A
AU  - Bender T
AU  - Brand F
AU  - Stieber C
AU  - Morawiec AM
AU  - Karakostas P
AU  - Schäfer VS
AU  - Bernsen S
AU  - Weydt P
AU  - Castro-Gomez S
AU  - Aziz A
AU  - Grobe-Einsler M
AU  - Kimmich O
AU  - Kobeleva X
AU  - Önder D
AU  - Lesmann H
AU  - Kumar S
AU  - Tacik P
AU  - Bhasin MA
AU  - Incardona P
AU  - Lee-Kirsch MA
AU  - Berner R
AU  - Schuetz C
AU  - Körholz J
AU  - Kretschmer T
AU  - Di Donato N
AU  - Schröck E
AU  - Heinen A
AU  - Reuner U
AU  - Hanßke AM
AU  - Kaiser FJ
AU  - Manka E
AU  - Munteanu M
AU  - Kuechler A
AU  - Cordula K
AU  - Hirtz R
AU  - Schlapakow E
AU  - Schlein C
AU  - Lisfeld J
AU  - Kubisch C
AU  - Herget T
AU  - Hempel M
AU  - Weiler-Normann C
AU  - Ullrich K
AU  - Schramm C
AU  - Rudolph C
AU  - Rillig F
AU  - Groffmann M
AU  - Muntau A
AU  - Tibelius A
AU  - Schwaibold EMC
AU  - Schaaf CP
AU  - Zawada M
AU  - Kaufmann L
AU  - Hinderhofer K
AU  - Okun PM
AU  - Kotzaeridou U
AU  - Hoffmann GF
AU  - Choukair D
AU  - Bettendorf M
AU  - Spielmann M
AU  - Ripke A
AU  - Pauly M
AU  - Münchau A
AU  - Lohmann K
AU  - Hüning I
AU  - Hanker B
AU  - Bäumer T
AU  - Herzog R
AU  - Hellenbroich Y
AU  - Westphal DS
AU  - Strom T
AU  - Kovacs R
AU  - Riedhammer KM
AU  - Mayerhanser K
AU  - Graf E
AU  - Brugger M
AU  - Hoefele J
AU  - Oexle K
AU  - Mirza-Schreiber N
AU  - Berutti R
AU  - Schatz U
AU  - Krenn M
AU  - Makowski C
AU  - Weigand H
AU  - Schröder S
AU  - Rohlfs M
AU  - Vill K
AU  - Hauck F
AU  - Borggraefe I
AU  - Müller-Felber W
AU  - Kurth I
AU  - Elbracht M
AU  - Knopp C
AU  - Begemann M
AU  - Kraft F
AU  - Lemke JR
AU  - Hentschel J
AU  - Platzer K
AU  - Strehlow V
AU  - Abou Jamra R
AU  - Kehrer M
AU  - Demidov G
AU  - Beck-Wödl S
AU  - Graessner H
AU  - Sturm M
AU  - Zeltner L
AU  - Schöls LJ
AU  - Magg J
AU  - Bevot A
AU  - Kehrer C
AU  - Kaiser N
AU  - Turro E
AU  - Horn D
AU  - Grüters-Kieslich A
AU  - Klein C
AU  - Mundlos S
AU  - Nöthen M
AU  - Riess O
AU  - Meitinger T
AU  - Krude H
AU  - Krawitz PM
AU  - Haack T
AU  - Ehmke N
AU  - Wagner M
PY  - 2025
JO  - Nature genetics
DO  - 10.1038/s41588-025-02271-6
UR  - https://doi.org/10.1038/s41588-025-02271-6
ER  -

APA

A, S., M, D., K, G., T, B., H, K., TC, H., H, E., S, P., A, K., S, M., L, A., F, B., HL, S., S, S., MA, M., JT, P., M, H., A, B., C, W., N, W., AA, S., C, S., J, N., T, K., AM, K., S, H., C, B., P, B., U, K., CE, O., M, S., HHP, N., S, H., C, G., T, R., F, B., N, M., S, S., C, P., E, M., M, K., K, C., RC, B., M, M., L, G., T, K., I, S., A, H., T, B., F, B., C, S., AM, M., P, K., VS, S., S, B., P, W., S, C., A, A., M, G., O, K., X, K., D, Ö., H, L., S, K., P, T., MA, B., P, I., MA, L., R, B., C, S., J, K., T, K., N, D. D., E, S., A, H., U, R., AM, H., FJ, K., E, M., M, M., A, K., K, C., R, H., E, S., C, S., J, L., C, K., T, H., M, H., C, W., K, U., C, S., C, R., F, R., M, G., A, M., A, T., EMC, S., CP, S., M, Z., L, K., K, H., PM, O., U, K., GF, H., D, C., M, B., M, S., A, R., M, P., A, M., K, L., I, H., B, H., T, B., R, H., Y, H., DS, W., T, S., R, K., KM, R., K, M., E, G., M, B., J, H., K, O., N, M., R, B., U, S., M, K., C, M., H, W., S, S., M, R., K, V., F, H., I, B., W, M., I, K., M, E., C, K., M, B., F, K., JR, L., J, H., K, P., V, S., R, A. J., M, K., G, D., S, B., H, G., M, S., L, Z., LJ, S., J, M., A, B., C, K., N, K., E, T., D, H., A, G., C, K., S, M., M, N., O, R., T, M., H, K., PM, K., T, H., N, E., & M, W. (2025). Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.. Nature genetics. https://doi.org/10.1038/s41588-025-02271-6

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pubmed · retrieved 2026-09-27T08:16:53.130Z