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Martin S. Taylor

ResearcherPublications, citations & collaboration network

Martin S. Taylor is a researcher indexed in PICO Portal from OpenAlex & ORCID.

How many works does Martin S. Taylor have?

PICO Portalindexed works

Martin S. Taylor has 147 works in the PICO Portal index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Martin S. Taylor have?

PICO Portalcitation count

Martin S. Taylor has 18,344 citations in the OpenAlex counts PICO Portal stores.

What is the h-index of Martin S. Taylor?

PICO Portalh-index

Martin S. Taylor has an h-index of 49 in OpenAlex.

What is the i10-index of Martin S. Taylor?

PICO Portali10-index

Martin S. Taylor has an i10-index of 80 in OpenAlex.

What is the ORCID of Martin S. Taylor?

PICO Portalorcid

The ORCID for Martin S. Taylor is on the source record.

What is the OpenAlex record for Martin S. Taylor?

PICO Portalopenalex

The OpenAlex for Martin S. Taylor is on the source record.

What are the most-cited papers on Martin S. Taylor?

PICO Portalmost cited works
CEP152 is a genome maintenance protein disrupted in Seckel syndrome
Ersan Kalay, Gökhan Yigit, Yakup Aslan, Karen Brown, Esther Pohl, Louise S. Bicknell, Hülya Kayserili, Yun Li, Beyhan Tüysüz, Gudrun Nürnberg, Wieland Kieß, Manfred Koegl, Ingelore Baessmann, Celal Kurtuluş Buruk, Bayram Toraman, Saadettin Kayıpmaz, Sibel Kul, Mevlit Íkbal, Daniel J. Turner, Martin S. Taylor, Jan Aerts, Carol Scott, Karen Milstein, Hélène Dollfus, Dagmar Wieczorek, Han G. Brunner, Matthew E. Hurles, Andrew P. Jackson, Anita Rauch, Peter Nürnberg, Ahmet Karagüzel, Bernd Wollnik
Nature Genetics. 2010228 CitationsOPEN ACCESS
Variant detection sensitivity and biases in whole genome and exome sequencing
Alison Meynert, Morad Ansari, David Fitzpatrick, Martin S. Taylor
BMC Bioinformatics. 2014226 CitationsOPEN ACCESS
Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism
Morad Ansari, Gemma Poke, Quentin R. V. Ferry, Kathleen A. Williamson, Roland Christopher Lochore Aldridge, Alison Meynert, Hemant Bengani, Cheng Yee Chan, Hülya Kayserili, Şahin Avcı, Raoul C. M. Hennekam, Anne Katrin Lampe, E. Redeker, Tessa Homfray, Alison Ross, Marie Falkenberg Smeland, Sahar Mansour, Michael Parker, Jacqueline Cook, Miranda Splitt, Richard B. Fisher, Alan Fryer, Alex Magee, Andrew O.M. Wilkie, Angela Barnicoat, Angela F. Brady, Nicola Cooper, Catherine Mercer, Charu Deshpande, Christopher Bennett, Daniela T. Pilz, Deborah Ruddy, Deirdre Cilliers, Diana Johnson, Dragana Josifova, Elisabeth Rosser, Elizabeth M. Thompson, Emma Wakeling, Esther Kinning, Fiona Stewart, Frances Flinter, Katta M. Girisha, Helen Cox, Helen V. Firth, Helen Kingston, Jamie S Wee, Jane A. Hurst, Jill Clayton‐Smith, John Tolmie, Julie Vogt, Katrina Tatton‐Brown, Kate Chandler, Katrina Prescott, Louise C. Wilson, Mahdiyeh Behnam, Meriel McEntagart, Rosemarie Davidson, Sally Ann Lynch, Sanjay M. Sisodiya, Sarju Mehta, Shane McKee, Shehla Mohammed, Simon Holden, Soo-Mi Park, Susan Holder, Victoria Harrison, Vivienne McConnell, Wayne Lam, Andrew Green, Dian Donnai, Maria Bitner‐Glindzicz, Deirdre E. Donnelly, Christoffer Nellåker, Martin S. Taylor, David Fitzpatrick
Journal of Medical Genetics. 2014172 CitationsOPEN ACCESS

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