I.D. Young

7.3k citations

32 papers · 1.6k indexed · 1 hit paper · h-index 17

Impact in

Developmental Biology top 5%
Structural Biology top 5%

Papers in ⓘ

Molecular Biology 13
- RNA and protein synthesis mechanisms 3
- RNA modifications and cancer 3
Genetics 8
- Connective tissue disorders research 4

Co-authors: Graeme Winter (2 shared papers)Richard J. Gildea (2 shared papers)Gwyndaf Evans (2 shared papers)David G. Waterman (2 shared papers)Nicholas K. Sauter (3 shared papers)James M. Parkhurst (2 shared papers)Aaron S. Brewster (2 shared papers)Markus Gerstel (1 shared paper)
Journals: Journal of Medical Genetics (13 papers)eLife (3 papers)Acta Crystallographica Section D Structural Biology (2 papers)Journal of Inherited Metabolic Disease (2 papers)Journal of Neurology Neurosurgery & Psychiatry (2 papers)
Partner nations: United Kingdom United States Japan

In The Last Decade

I.D. Young

32 papers receiving 1.6k citations

Hit Papers

align trajectories log scale

DIALS: implementation and evaluation of a new integration package 2018 · 723 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2018 Acta Crystallographica Section D Structural Biology

Peers

Countries citing papers authored by I.D. Young

Since Specialization

Citations

This map shows the geographic impact of I.D. Young's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by I.D. Young with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites I.D. Young more than expected).

Fields of papers citing papers by I.D. Young

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by I.D. Young. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by I.D. Young. The network helps show where I.D. Young may publish in the future.

Co-authors

The 25 scholars most cited alongside I.D. Young, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with I.D. Young Line = papers co-authored together I.D. Young links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 32 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	DIALS: implementation and evaluation of a new integration package Acta Crystallographica Section D Structural Biology ·Graeme Winter, David G. Waterman, James M. Parkhurst, Aaron S. Brewster, Richard J. Gildea, Markus Gerstel, Luis Fuentes‐Montero, M. Vollmar, Tara Michels-Clark, I.D. Young, Nicholas K. Sauter, Gwyndaf Evans Hit paper breakdown →	2018	723
2	The Mutational Spectrum of the Sonic Hedgehog Gene in Holoprosencephaly: SHH Mutations Cause a Significant Proportion of Autosomal Dominant Holoprosencephaly Human Molecular Genetics ·Luisa Nanni, Jeffrey E. Ming, Maureen Bocian, Kathryn A. Steinhaus, Diana W. Bianchi, Christine de Die‐Smulders, Aldo Giannotti, K Imaizumi, Kenneth Lyons Jones, Miguel Del Campo, R. A. Martin, P. Meinecke, Mary Ella Pierpont, Nathaniel H. Robin, I.D. Young, Erich Roessler, Maximilian Muenke	1999	274
3	Holt-Oram syndrome: a clinical genetic study. Journal of Medical Genetics ·Ruth Newbury‐Ecob, R Leanage, J. A. Raeburn, I.D. Young	1996	173
4	Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations — molecular and audiological findings International Journal of Pediatric Otorhinolaryngology ·R F Mueller, A Nehammer, Anna Middleton, Mark Houseman, Graham R. Taylor, M Bitner-Glindzciz, Guy Van Camp, Michael Parker, I.D. Young, Adrian Davis, Valerie Newton, Nicholas Lench	1999	51
5	Structural changes correlated with magnetic spin state isomorphism in the S₂ state of the Mn₄CaO₅ cluster in the oxygen-evolving complex of photosystem II Chemical Science ·Ruchira Chatterjee, Guangye Han, Jan Kern, Sheraz Gul, Franklin D. Fuller, Anna Garachtchenko, I.D. Young, Tsu-Chien Weng, Dennis Nordlund, Roberto Alonso‐Mori, Uwe Bergmann, Dimosthenis Sokaras, Makoto Hatakeyama, Vittal K. Yachandra, Junko Yano	2016	40
6	Inherited Disorders of the Skeleton Journal of Medical Genetics ·I.D. Young	1989	39
7	Hereditary distal spinal muscular atrophy with vocal cord paralysis. Journal of Neurology Neurosurgery & Psychiatry ·I.D. Young, Peter S. Harper	1980	39
8	Structural basis for context-specific inhibition of translation by oxazolidinone antibiotics Nature Structural & Molecular Biology ·Kaitlyn Tsai, Vanja Stojković, D. John Lee, I.D. Young, Teresa Szal, Dorota Klepacki, Nora Vázquez‐Laslop, Alexander S. Mankin, James S. Fraser, Danica Galonić Fujimori	2022	38
9	Improving signal strength in serial crystallography with DIALS geometry refinement Acta Crystallographica Section D Structural Biology ·Aaron S. Brewster, David G. Waterman, James M. Parkhurst, Richard J. Gildea, I.D. Young, L. ORiordan, Junko Yano, Graeme Winter, Gwyndaf Evans, Nicholas K. Sauter	2018	30
10	Structural isomers of the S₂ state in photosystem II: do they exist at room temperature and are they important for function? Physiologia Plantarum ·Ruchira Chatterjee, Louise Lassalle, Sheraz Gul, Franklin D. Fuller, I.D. Young, Mohamed Ibrahim, Casper de Lichtenberg, Mun Hon Cheah, Athina Zouni, Johannes Messinger, Vittal K. Yachandra, Jan Kern, Junko Yano	2019	28
11	Familial calcification of the basal ganglia with cerebrospinal fluid pleocytosis. Journal of Medical Genetics ·Lalit Mehta, J Q Trounce, Jacqueline Moore, I.D. Young	1986	21
12	A lethal skeletal dysplasia with generalised sclerosis and advanced skeletal maturation: Blomstrand chondrodysplasia? Journal of Medical Genetics ·I.D. Young, Jane Zuccollo, N J Broderick	1993	19
13	Neuraminidase deficiency: case report and review of the phenotype. Journal of Medical Genetics ·I.D. Young, Elisabeth Young, Jean Mossman, Alistair R. Fielder, Jeffrey R. Moore	1987	19
14	Directed evolution of the rRNA methylating enzyme Cfr reveals molecular basis of antibiotic resistance eLife ·Kaitlyn Tsai, Vanja Stojković, Lianet Noda‐García, I.D. Young, Alexander G. Myasnikov, Jordan Kleinman, Ali Palla, Stephen N. Floor, Adam Frost, James S. Fraser, Dan S. Tawfik, Danica Galonić Fujimori	2021	17
15	Assessment of the nucleotide modifications in the high-resolution cryo-electron microscopy structure of the Escherichia coli 50S subunit Nucleic Acids Research ·Vanja Stojković, Alexander G. Myasnikov, I.D. Young, Adam Frost, James S. Fraser, Danica Galonić Fujimori	2020	17
16	Hereditary Hearing Loss and its Syndromes, 2nd edn Journal of Medical Genetics ·I.D. Young	2005	16
17	Clinical Genetics: Problems in Diagnosis and Counseling Journal of Medical Genetics ·I.D. Young	1983	16
18	Lethal skeletal dysplasia owing to double heterozygosity for achondroplasia and spondyloepiphyseal dysplasia congenita. Journal of Medical Genetics ·I.D. Young, N R Ruggins, J. M. Somers, Jane Zuccollo, N Rutter	1992	10
19	Variations in genetic assessment and recurrence risks quoted for childhood deafness: a survey of clinical geneticists Journal of Medical Genetics ·Michael Parker, Heather Fortnum, I.D. Young, Adrian Davis	1999	7
20	Fumarate hydratase deficiency: increased fumaric acid in amniotic fluid of two affected pregnancies Journal of Inherited Metabolic Disease ·N. J. Manning, S. E. Olpin, R. J. Pollitt, M. Downing, A F Heeley, I.D. Young	2000	6

About I.D. Young

I.D. Young is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Pediatrics, Perinatology and Child Health and Oncology, having authored 32 papers that have together received 1.6k indexed citations. Recurring topics across this work include Connective tissue disorders research (4 papers), Bone health and treatments (3 papers), RNA and protein synthesis mechanisms (3 papers), RNA modifications and cancer (3 papers), Enzyme Structure and Function (3 papers), Invertebrate Immune Response Mechanisms (2 papers), Advanced X-ray Imaging Techniques (2 papers) and Medical Imaging and Pathology Studies (2 papers). The work is most often cited by research in Developmental Biology (54 citations), Structural Biology (33 citations), Molecular Biology (1.1k citations), Sensory Systems (68 citations) and Genetics (379 citations). I.D. Young has collaborated with scholars based in United Kingdom, United States and Japan. Frequent co-authors include Graeme Winter, Richard J. Gildea, Gwyndaf Evans, David G. Waterman, Nicholas K. Sauter, James M. Parkhurst, Aaron S. Brewster, Markus Gerstel, Tara Michels-Clark and M. Vollmar. Their work appears in journals such as Journal of Medical Genetics, eLife, Acta Crystallographica Section D Structural Biology, Journal of Inherited Metabolic Disease and Journal of Neurology Neurosurgery & Psychiatry.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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