Andreas W. Kuss

Overview

Best Publications

• Deep sequencing reveals 50 novel genes for recessive cognitive disorders

  Hossein Najmabadi;Hao Hu;Masoud Garshasbi;Tomasz Zemojtel

  1052
  Citations

• Mutations in NSUN2 cause autosomal-recessive intellectual disability

  Lia Abbasi-Moheb;Sara Mertel;Melanie Gonsior;Leyla Nouri-Vahid

  288
  Citations

• Somatic Mutation Profiles of MSI and MSS Colorectal Cancer Identified by Whole Exome Next Generation Sequencing and Bioinformatics Analysis

  Bernd Timmermann;Martin Kerick;Christina Roehr;Christina Roehr;Axel Fischer

  266
  Citations

• TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy.

  Alena Cízková;Viktor Stránecký;Johannes A Mayr;Markéta Tesarová

  253
  Citations

• A defect in the ionotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardation.

  Mohammad Mahdi Motazacker;Benjamin Rainer Rost;Tim Hucho;Masoud Garshasbi

  223
  Citations

• Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene

  Joanna Walczak-Sztulpa;Jonathan Eggenschwiler;Daniel Osborn;Desmond A. Brown

  218
  Citations

• Identification of Mutations in TRAPPC9, which Encodes the NIK- and IKK-β-Binding Protein, in Nonsyndromic Autosomal-Recessive Mental Retardation

  Asif Mir;Liana Kaufman;Abdul Noor;Mahdi M. Motazacker

  183
  Citations

• A defect in the TUSC3 gene is associated with autosomal recessive mental retardation.

  Masoud Garshasbi;Valeh Hadavi;Haleh Habibi;Kimia Kahrizi

  177
  Citations

• CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait

  Seval Türkmen;Gao Guo;Masoud Garshasbi;Katrin Hoffmann

  160
  Citations

• Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci.

  Hossein Najmabadi;Mohammad Mahdi Motazacker;Masoud Garshasbi;Kimia Kahrizi

  158
  Citations

• Novel JARID1C/SMCX mutations in patients with X-linked mental retardation.

  Andreas Tzschach;Steffen Lenzner;Bettina Moser;Richard Reinhardt

  157
  Citations

• ST3GAL3 mutations impair the development of higher cognitive functions

  Hao Hu;Katinka Eggers;Wei Chen;Masoud Garshasbi

  125
  Citations

• Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium.

  Arjan P.M. de Brouwer;Helger G. Yntema;Tjitske Kleefstra;Dorien Lugtenberg

  121
  Citations

• A clinical and molecular genetic study of 112 Iranian families with primary microcephaly

  H. . Darvish;Sahar Esmaeeli Nieh;G. B. Monajemi;M. Mohseni

  117
  Citations

• CCDC22 deficiency in humans blunts activation of proinflammatory NF-kappa B signaling

  Petro Starokadomskyy;Nathan Gluck;Nathan Gluck;Haiying Li;Baozhi Chen

  117
  Citations

• Long noncoding RNA NEAT1 modulates immune cell functions and is suppressed in early onset myocardial infarction patients.

  Martina Gast;Bernhard H Rauch;Arash Haghikia;Shinichi Nakagawa

  103
  Citations

• Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability

  Muhammad Arshad Rafiq;Andreas W. Kuss;Lucia Puettmann;Abdul Noor

  101
  Citations

• Immune system-mediated atherosclerosis caused by deficiency of long non-coding RNA MALAT1 in ApoE-/-mice.

  Martina Gast;Bernhard H Rauch;Shinichi Nakagawa;Arash Haghikia

  100
  Citations

• SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly

  Masoud Garshasbi;Mohammad Mahdi Motazacker;Kimia Kahrizi;Farkhondeh Behjati

  100
  Citations

• Mutation of the conserved polyadenosine RNA binding protein, ZC3H14/dNab2, impairs neural function in Drosophila and humans

  ChangHui Pak;Masoud Garshasbi;Kimia Kahrizi;Christina Gross

  92
  Citations