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D-Index & Metrics

Biology and Biochemistry

D-Index
52
Citations
13028
World Ranking
16516
National Ranking
1303

Overview

Susan Lindsay is a researcher affiliated with Newcastle University in the United Kingdom, specializing in the fields of Biochemistry, Genetics, and Molecular Biology. Their work spans several subfields, including Molecular Biology, Genetics, and Developmental and Educational Psychology.

Their research focuses on multiple topics such as:

  • CRISPR and Genetic Engineering
  • Genomics and Rare Diseases
  • RNA and protein synthesis mechanisms
  • Hedgehog Signaling Pathway Studies
  • Epigenetics and DNA Methylation
  • Cleft Lip and Palate Research
  • Genetics and Neurodevelopmental Disorders

Among their recent publications are:

  • "Saturation genome editing of DDX3X clarifies pathogenicity of germline and somatic variation" (2022), published in bioRxiv (Cold Spring Harbor Laboratory)
  • "Mutations in phospholipase C eta-1 (PLCH1) are associated with holoprosencephaly" (2021), published in Journal of Medical Genetics
  • "Development of the early fetal human thalamus: from a protomap to emergent thalamic nuclei" (2025), published in Frontiers in Neuroanatomy

Frequent collaborators in their publications include Elizabeth J. Radford, H.K. Tan, Malin H. L. Andersson, James Stephenson, and Eugene J. Gardner.

The publication venues where Susan Lindsay has contributed most frequently are:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Journal of Medical Genetics
  • Frontiers in Neuroanatomy

The combination of genetics, molecular biology, and developmental psychology in their work illustrates a multidisciplinary approach to understanding complex biological and neurodevelopmental processes.

Best Publications

  • Mapping copy number variation by population-scale genome sequencing

    Ryan E. Mills;Klaudia Walter;Chip Stewart;Robert E. Handsaker

  • Gene expression across mammalian organ development

    Margarida Cardoso-Moreira;Margarida Cardoso-Moreira;Jean Halbert;Delphine Valloton;Britta Velten

  • Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance

    Max A. Tischfield;Hagit N. Baris;Chen Wu;Guenther Rudolph

  • Single-cell transcriptomes from human kidneys reveal the cellular identity of renal tumors

    Matthew D. Young;Thomas J. Mitchell;Thomas J. Mitchell;Thomas J. Mitchell;Felipe A. Vieira Braga;Maxine G. B. Tran

  • Decoding human fetal liver haematopoiesis

    Dorin-Mirel Popescu;Rachel A. Botting;Emily Stephenson;Kile Green

  • The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome

    Mark Clement-Jones;Simone Schiller;Ercole Rao;Rüdiger J. Blaschke

  • Use of restriction enzymes to detect potential gene sequences in mammalian DNA

    Susan Lindsay;Adrian P. Bird

  • SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development

    N.A Hanley;D.M Hagan;M Clement-Jones;S.G Ball

  • Spatiotemporal immune zonation of the human kidney

    Benjamin J. Stewart;Benjamin J. Stewart;Benjamin J. Stewart;John R. Ferdinand;Matthew D. Young;Thomas J. Mitchell;Thomas J. Mitchell;Thomas J. Mitchell

  • WDR62 is associated with the spindle pole and is mutated in human microcephaly

    Adeline K. Nicholas;Maryam Khurshid;Julie Désir;Ofélia P. Carvalho

  • A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis

    Alison J. Ross;Victor Ruiz-Perez;Yiming Wang;Donna Marie Hagan

  • Hepatic Differentiation of Murine Embryonic Stem Cells

    Elizabeth A. Jones;David Tosh;David I. Wilson;Susan Lindsay

  • Autosomal dominant sacral agenesis: Currarino syndrome

    Sally Ann Lynch;Yiming Wang;T Strachan;John Burn

  • Expression of steroidogenic factor 1 and Wilms' tumour 1 during early human gonadal development and sex determination.

    N.A. Hanley;N.A. Hanley;S.G. Ball;M. Clement-Jones;D.M. Hagan

  • Disrupted alternative splicing for genes implicated in splicing and ciliogenesis causes PRPF31 retinitis pigmentosa.

    Adriana Buskin;Lili Zhu;Valeria Chichagova;Basudha Basu

  • A Molecular Neuroanatomical Study of the Developing Human Neocortex from 8 to 17 Postconceptional Weeks Revealing the Early Differentiation of the Subplate and Subventricular Zone

    Nadhim Bayatti;Jennifer A. Moss;Li Sun;Philip Ambrose

  • Human–mouse differences in the embryonic expression patterns of developmental control genes and disease genes

    Francoise Fougerousse;Philip Bullen;Muriel Herasse;Susan Lindsay

  • Human CHN1 Mutations Hyperactivate α2-Chimaerin and Cause Duane's Retraction Syndrome

    Noriko Miyake;Noriko Miyake;John Chilton;Maria Psatha;Long Cheng;Long Cheng

  • The Essential Role of Centrosomal NDE1 in Human Cerebral Cortex Neurogenesis

    Mehmet Bakircioglu;Ofélia P. Carvalho;Maryam Khurshid;James J. Cox

  • Hepatic differentiation of murine embryonic stem cells

    Elizabeth A. Jones;David Tosh;Susan Lindsay;David I. Wilson

Frequent Co-Authors

Tom Strachan
Tom Strachan Newcastle University
Majlinda Lako
Majlinda Lako Newcastle University
Sam Behjati
Sam Behjati Wellcome Sanger Institute
Muzlifah Haniffa
Muzlifah Haniffa Newcastle University
Stephen C. Robson
Stephen C. Robson Newcastle University
Sarah A. Teichmann
Sarah A. Teichmann University of Cambridge
Shomi S. Bhattacharya
Shomi S. Bhattacharya University College London
Kay E. Davies
Kay E. Davies University of Oxford
Andrew J. Copp
Andrew J. Copp University College London
John Burn
John Burn Newcastle University

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