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Genetics

D-Index
64
Citations
18186
World Ranking
2769
National Ranking
1217

Overview

Yiping Shen is affiliated with Claritas Genomics in the United States. Their research contributions span multiple fields within biochemistry, genetics, molecular biology, and medicine, with a significant focus on genetics and related subfields.

They have published extensively in genetics and molecular biology, contributing to topics such as genetics and neurodevelopmental disorders, genomic variations and chromosomal abnormalities, and genomics of rare diseases. Other areas of interest include congenital heart defects research, prenatal screening and diagnostics, as well as catalytic processes in materials science and gas sensing nanomaterials and sensors.

Their recent publications highlight a range of subjects and publication venues. Selected papers include:

  • De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders, 2022, Science Advances
  • CQDs improved the photoelectrocatalytic performance of plasma assembled WO3/TiO2-NRs for bisphenol A degradation, 2022, Journal of Hazardous Materials
  • De novo variants in the Helicase-C domain of CHD8 are associated with severe phenotypes including autism, language disability and overgrowth, 2020, Human Genetics
  • A High Proportion of Novel ACAN Mutations and Their Prevalence in a Large Cohort of Chinese Short Stature Children, 2021, The Journal of Clinical Endocrinology & Metabolism
  • The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chromosomes, 2022, Human Genetics and Genomics Advances

Their research has been disseminated through a variety of academic publication venues, notably including:

  • PubMed
  • Frontiers in Genetics
  • Molecular Genetics & Genomic Medicine
  • SSRN Electronic Journal
  • Clinica Chimica Acta

Yiping Shen frequently collaborates with other researchers. Some of the most frequent co-authors associated with their work are:

  • Zailong Qin
  • Jingsi Luo
  • Shang Yi
  • Dijiong Wu
  • Mengting Li

Their research contributions encompass important facets of genetic and molecular investigations, including work in pediatrics, perinatology, and child health, as well as emerging interests in renewable energy, sustainability, and environmental sciences.

Best Publications

  • Association between Microdeletion and Microduplication at 16p11.2 and Autism

    Lauren A. Weiss;Yiping Shen;Joshua M. Korn;Joshua M. Korn;Dan E. Arking

  • Association between microdeletion and microduplication at 16p11.2 and autism

    Lauren A. Weiss;Yiping Shen;Joshua M. Korn;Dan E. Arking

  • Disruption of Neurexin 1 Associated with Autism Spectrum Disorder

    Hyung Goo Kim;Shotaro Kishikawa;Anne W. Higgins;Ihn Sik Seong

  • Induced Pluripotent Stem Cells from Patients with Huntington’s Disease : Show CAG Repeat-Expansion-Associated Phenotypes

    Virginia B. Mattis;Soshana P. Svendsen;Allison Ebert;Clive N. Svendsen

  • Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries

    Michael E. Talkowski;Jill A. Rosenfeld;Ian Blumenthal;Vamsee Pillalamarri

  • Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

    Sébastien Jacquemont;Alexandre Reymond;Flore Zufferey;Louise Harewood

  • Clinical Genetic Testing for Patients With Autism Spectrum Disorders

    Yiping Shen;Kira A. Dies;Ingrid A. Holm;Carolyn Bridgemohan

  • Genomic dissection of population substructure of Han Chinese and its implication in association studies.

    Shuhua Xu;Xianyong Yin;Shilin Li;Wenfei Jin

  • Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

    David T. Miller;Yiping Shen;Lauren A. Weiss;Joshua Korn

  • Somatic mutations in cerebral cortical malformations

    Saumya S. Jamuar;Anh Thu N Lam;Martin Kircher;Alissa M. D'Gama

  • A Genome-Wide Search for Signals of High Altitude Adaptation in Tibetans

    Shuhua Xu;Shilin Li;Yajun Yang;Jingze Tan

  • Deletions of NRXN1 (Neurexin-1) Predispose to a Wide Spectrum of Developmental Disorders

    Michael S L Ching;Yiping Shen;Yiping Shen;Wen-Hann Tan;Wen-Hann Tan;Shafali S Jeste;Shafali S Jeste

  • A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

    Flore Zufferey;Elliott H. Sherr;Noam D. Beckmann;Ellen Hanson

  • Downregulated MicroRNA-200a in Meningiomas Promotes Tumor Growth by Reducing E-Cadherin and Activating the Wnt/β-Catenin Signaling Pathway

    Okay Saydam;Yiping Shen;Thomas Würdinger;Thomas Würdinger;Ozlem Senol

  • Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration

    Colby Chiang;Jessie C Jacobsen;Carl Ernst;Carrie Hanscom

  • Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.

    Debra D'Angelo;Sébastien Lebon;Qixuan Chen;Sandra Martin-Brevet

  • Assessment of 2q23.1 Microdeletion Syndrome Implicates MBD5 as a Single Causal Locus of Intellectual Disability, Epilepsy, and Autism Spectrum Disorder

    Michael E. Talkowski;Sureni V. Mullegama;Jill A. Rosenfeld;Bregje W M Van Bon

  • Angiogenin Loss-of-Function Mutations in Amyotrophic Lateral Sclerosis

    David Wu;Wenhao Yu;Hiroko Kishikawa;Rebecca D. Folkerth

  • Next-generation sequencing strategies enable routine detection of balanced chromosome rearrangements for clinical diagnostics and genetic research.

    Michael E. Talkowski;Michael E. Talkowski;Carl Ernst;Adrian Heilbut;Colby Chiang

  • Genomic profiling distinguishes familial multiple and sporadic multiple meningiomas

    Yiping Shen;Fabio Nunes;Anat Stemmer-Rachamimov;Marianne James

Frequent Co-Authors

Bai-Lin Wu
Bai-Lin Wu Claritas Genomics (United States)
James F. Gusella
James F. Gusella Harvard University
Cynthia C. Morton
Cynthia C. Morton Brigham and Women's Hospital
Michael E. Talkowski
Michael E. Talkowski Harvard University
Mark J. Daly
Mark J. Daly Massachusetts General Hospital
Joel N. Hirschhorn
Joel N. Hirschhorn Boston Children's Hospital
Marcy E. MacDonald
Marcy E. MacDonald Harvard University
Douglas M. Ruderfer
Douglas M. Ruderfer Vanderbilt University Medical Center
Jill A. Rosenfeld
Jill A. Rosenfeld Baylor College of Medicine
Jacques S. Beckmann
Jacques S. Beckmann University of Lausanne

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