Andreas W. Kuss

Andreas W. Kuss publication distribution in Molecular Biology in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Molecular Biology in 2026. The highlighted bar marks where Andreas W. Kuss sits on this spectrum.

Andreas W. Kuss D-index placement in Molecular Biology in 2026

The chart shows the D-index (discipline H-index) distribution of Molecular Biology scientists ranked by Research.com in 2026. The highlighted bar marks where Andreas W. Kuss sits on this spectrum.

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