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研究兴趣

论文共 56 篇作者统计合作学者相似作者

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A Diagnosis of Vascular EDS in Childhood: Clinical and Molecular Features of 60 Individuals
Niamh Wilkinson, Elena Cervi, Bart Wagner, Katherine Von-Klemperer, Toby Andrew,Neeti Ghali, Fleur Van Dijk
EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 404-404
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Auditing Genetic Testing for Aortopathy at the Genomics Laboratory in Royal Brompton & Harefield Hospital
Shao Ting, Pearlyn Lee,Matthew Edwards,Andrew Fleming,Neeti Ghali, Juliette Harris, Deborah Morris-Rosendahl,Christoph Nienaber, Fortunate Rusike, Fleur Van Dijk
EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 287-287
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A Unique Collaborative Model Providing Supportive and Self-Advocacy Tools to the Rare Disease Community
Juliette M. Harris, Jacqui Fish, Jared Griffin, Gemma Hasnaoui, Clare Stacey,Neeti Ghali,Fleur S. van Dijk
Rare (2024): 100026-100026
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New Insights from Five Cases of Spondylodysplastic Ehlers Danlos Syndrome
Rhoda Akilapa, Fleur Van Dijk, Deborah Shears, Laura Watts,Alistair Calder,Lucy Loong,Neeti Ghali
EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 401-401
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Vascular EDS in Adulthood: an Overview of Clinical and Molecular Features of 151 Individuals
Niamh Wilkinson, Katherine Von-Klemperer, Elena Cervi,Duncan Baker,Chloe Angwin,Juliette Harris, Michael Pope, Ravinder Sehra,Neeti Ghali, Fleur Van Dijk
EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 404-404
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Large-scale Evaluation of Outcomes Following a Genetic Diagnosis in Children with Severe Developmental Disorders
Harriet Copeland,Karen J Low,Sarah Wynn, Ayesha Ahmed, Victoria Arthur,Meena Balasubramanian, Katya Bennett,Jonathan Berg,Marta Bertoli,Lisa Bryson, Catrin Bucknall,Jamie Campbell,Kate Chandler,Jaynee Chauhan, Amy Clarkson, Rachel Coles, Hector Conti,Philandra Costello, Tessa Coupar, Amy Craig,John Dean, Amy Dillon,Abhijit Dixit, Kathryn Drew,Jacqueline Eason,Francesca Forzano,Nicky Foulds,Alice Gardham,Neeti Ghali,Andrew Green, William Hanna,Rachel Harrison, Mairead Hegarty,Jenny Higgs,Muriel Holder,Rachel Irving,Vani Jain,Katie Johnson, Rachel Jolley,Wendy Jones,Gabriela Jones,Shelagh Joss, Ruta Kalinauskiene, Farah Kanini,Karl Kavanagh, Mahmudur Khan,Naz Khan,Emma Kivuva,Nayana Lahiri, Neeta Lakhani,Anne Lampe,Sally Ann Lynch,Sahar Mansour, Alice Marsden, Hannah Massey,Shane McKee,Shehla Mohammed,Swati Naik, Mithushanaa Nesarajah,Ruth Newbury-Ecob, Fiona Osborne,Michael J Parker,Jenny Patterson,Caroline Pottinger,Matina Prapa,Katrina Prescott, Shauna Quinn,Jessica A Radley,Sarah Robart,Alison Ross,Giulia Rosti,Francis Sansbury,Ajoy Sarkar,Claire Searle,Nora Shannon,Debbie Shears,Sarah Smithson,Helen Stewart,Mohnish Suri,Shereen Tadros, Rachel Theobald, Rhian Thomas, Olga Tsoulaki,Pradeep Vasudevan, Maribel Verdesoto,Emma Vittery, Sinead Whyte,Emily Woods,Thomas Wright,David Zocche,Helen V Firth,Caroline F Wright,the DDD Study
Genetics in Medicine Open (2024)
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Angiographic and Clinical Findings in a Cohort of Patients with Spontaneous Coronary Artery Dissection and Vascular Ehlers-Danlos Syndrome
Neeti Ghali, Andrew Deaner, Nigel Wheeldon,Chloe Angwin,Diana Johnson,Glenda Sobey, Katherine Von-Klemperer, Sylvia Keigwin,Duncan Baker, Katherine Read,David Adlam, Fleur Van Dijk
EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 414-414
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The Natural History of Classical Ehlers Danlos Syndrome in Adults and Children
Chloe Angwin, Niamh Wilkinson,Duncan Baker,Juliette Harris, Michael Pope, Ravinder Sehra,Neeti Ghali, Fleur Van Dijk
EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 398-398
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作者统计

#Papers: 56

#Citation: 1891

H-Index: 16

G-Index: 34

Sociability: 7

Diversity: 2

Activity: 13

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