Artikel

in Proc Natl Acad Sci U S A

ENHANCED GRAVITROPISM 2 encodes a STERILE ALPHA MOTIF–containing protein that controls root growth angle in barley and wheat

  • G.K. Kirschner
  • S. Rosignoli
  • L. Guo
  • I. Vardanega
  • J. Imani
  • J. Altmüller
  • S.G. Milner
  • R: Balzano
  • K.A. Nagel
  • D. Pflugfelder
  • C. Forestan
  • R. Bovina
  • R. Koller
  • T.G. Stöcker
  • M. Mascher
  • J. Simmonds
  • C. Uauy
  • H. Schoof
  • R. Tuberosa
  • S. Salvi
  • F. Hochholdinger
in Eur J Med Genet

MFSD2A-associated primary microcephaly - expanding the clinical and mutational spectrum of this ultra-rare disease

  • K. Khuller
  • G. Yigit
  • C. Martínez Grijalva
  • J. Altmüller
  • H. Thiele
  • P. Nürnberg
  • N.H. Elcioglu
  • B. Yeter
  • U. Hehr
  • A. Stein
  • A. Della Marina
  • A. Köninger
  • C. Depienne
  • F.J. Kaiser
  • B. Wollnik
  • A. Kuechler
in Int J Mol Sci

Altered DNA methylation profiles in SF3B1 mutated CLL patients

  • A. Pacholewska
  • C. Grimm
  • C.D. Herling
  • M. Lienhard
  • A. Königs
  • B. Timmermann
  • J. Altmüller
  • O. Mücke
  • H.C. Reinhardt
  • C. Plass
  • R. Herwig
  • M. Hallek
  • M.R. Schweiger
in Nature

Unravelling the collateral damage of antibiotics on gut bacteria

  • L. Maier
  • C.V. Goemans
  • J. Wirbel
  • M. Kuhn
  • C. Eberl
  • M. Pruteanu
  • P. Müller
  • S. Garcia-Santamarina
  • E. Cacace
  • B. Zhang
  • C. Gekeler
  • T. Banerjee
  • E.E. Anderson
  • A. Milanese
  • U. Löber
  • S.K. Forslund
  • K.R. Patil
  • M. Zimmermann
  • B. Stecher
  • G. Zeller
  • P. Bork
  • A. Typas
in Eur J Hum Genet

Familial cleft tongue caused by a unique translation initiation codon variant in TP63

  • J. Schmidt
  • G. Schreiber
  • J. Altmüller
  • H. Thiele
  • P. Nürnberg
  • Y. Li
  • S. Kaulfuß
  • R. Funke
  • B. Wilken
  • G. Yigit
  • B. Wollnik
in J Am Soc Nephrol

mTOR-activating mutations in RRAGD are causative for kidney tubulopathy and cardiomyopathy

  • K.P. Schlingmann
  • F. Jouret
  • K. Shen
  • A. Nigam
  • F. Arjona
  • C. Dafinger
  • P. Houillier
  • D. Jones
  • F. Kleinerüschkamp
  • J. Oh
  • N. Godefroid
  • M. Eltan
  • T. Güran
  • S. Burtey
  • M.C. Parotte
  • J. König
  • A. Braun
  • C. Bos
  • M.I. Serra
  • H. Rehmann
  • F. Zwartkruis
  • K. Renkema
  • K. Klingel
  • E. Schulze-Bahr
  • B. Schermer
  • C. Bergmann
  • J. Altmüller
  • H. Thiele
  • B. Beck
  • K. Dahan
  • D. Sabatini
  • M. Liebau
  • R. Vargas-Poussou
  • N. Knoers
  • M. Konrad
  • J. de Baaij
in Am J Med Genet A

Genomic basis of syndromic short stature in an Algerian patient cohort

  • S. Moosa
  • F. Chentli
  • J. Altmüller
  • N. Bögershausen
  • P. Nürnberg
  • G. Yigit
  • Y. Li
  • B. Wollnik
in Eur J Neurol

Retinoids are not linked to risk of multiple sclerosis: a Danish nationwide cohort study

  • F. Cortes-Figueiredo
  • N.M. Nielsen
  • E. Stenager
  • F. Paul
  • J. Hallas
  • K.B. Kristensen
in Genes

A homozygous AKNA frameshift variant is associated with microcephaly in a Pakistani family

  • S.S. Waseem
  • A. Moawia
  • B. Budde
  • M. Tariq
  • A. Khan
  • Z. Ali
  • S. Khan
  • M. Iqbal
  • N.A. Malik
  • S.U. Haque
  • J. Altmüller
  • H. Thiele
  • M.S. Hussain
  • S. Cirak
  • S.M. Baig
  • P. Nürnberg
in BMC Nephrol

Hemophagocytic lymphohistiocytosis and thrombotic microangiopathy after parvovirus B19 infection and renal transplantation: a case report

  • C.J. Steffen
  • N. Koch
  • K.U. Eckardt
  • K. Amann
  • E. Seelow
  • A. Schreiber