I D Young

5.1k citations

79 papers · 3.6k indexed · 1 hit paper · h-index 26

Impact in

Genetics top 0.5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Animal Genetics and Reproduction
- Connective tissue disorders research
Reproductive Medicine top 2%
- Sperm and Testicular Function

Papers in

Developmental Biology 4
Genetics 42
- Connective tissue disorders research 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 6
- BRCA gene mutations in cancer 4

Co-authors: P.S. Harper J. David Brook Silvana Guioli Sahar Mansour M. Dominguez-Steglich Cheni Kwok Jamie W. Foster Peter N. Goodfellow
Journals: Journal of Medical Genetics (17 papers)Clinical Genetics (6 papers)Journal of Intellectual Disability Research (4 papers)Developmental Medicine & Child Neurology (3 papers)The Lancet (3 papers)
Partner nations: United Kingdom United States France

In The Last Decade

I D Young

78 papers receiving 3.5k citations

Hit Papers

align trajectories log scale

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene 1994 · 1.2k citations

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-authorship network

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

#	Work
1	A systems genetics approach identifies roles for proteasome factors in heart development and congenital heart defects PLoS Genetics ·Gist H. Farr, 光也細山, Elin Hidmark, Nicholas Christopher, I D Young, H Ghasemnejad, Aaron Olson, David R. Beier, Lisa Maves	2025	1
2	Introduction to Risk Calculation in Genetic Counseling I D Young	2006	14
3	Clinical and genetic heterogeneity in Desbuquois dysplasia American Journal of Medical Genetics Part A ·Laurence Faivre, Martine Le Merrer, Klaus Zerres, M. Ben Hariz, Déborah Scheffer, I D Young, P Maroteaux, Arnold Münnich, Valérie Cormier‐Daire	2004	19
4	Trisomy 13 and trisomy 18 in a defined population: epidemiological, genetic and prenatal observations Prenatal Diagnosis ·Pedro Fauth Manhães Miranda, J. L. S. Budd, Elizabeth S. Draper, I D Young	2003	48
5	Somatic and Germline Mosaic Mutations in the doublecortin Gene Are Associated with Variable Phenotypes The American Journal of Human Genetics ·Joseph G. Gleeson, Sharon Minnerath, Ruben Kuzniecky, William B. Dobyns, I D Young, M. Elizabeth Ross, Christopher A. Walsh	2000	87
6	Inactivating Mutation in the Human Parathyroid Hormone Receptor Type 1 Gene in Blomstrand Chondrodysplasia Endocrinology ·Andrew C. Karaplis, Bin He, Matthew Nguyen, I D Young, D Semeraro, Hidehiro Ozawa, Norio Amizuka	1998	97
7	Achondroplasia: a case of neglect? The Lancet ·I D Young	1998	11
8	Chronic tubulo-interstitial nephropathy in children with cranioectodermal dysplasia Pediatric Nephrology ·Mông- Lan, I D Young, Robert J. Cunningham, I. D. Ansell, Jonathan HC Evans	1997	7
9	The role of SOX9 in autosomal sex reversal and campomelic dysplasia Philosophical Transactions of the Royal Society B Biological Sciences ·Alan J. Schafer, M. Dominguez-Steglich, Silvana Guioli, Cheni Kwok, P A Weller, Milena Stevanović, J. Weissenbach, Sahar Mansour, I D Young, Peter N. Goodfellow, (unknown), (unknown)	1995	25
10	Holt–Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q Nature Genetics ·Jonathan Terrett, Ruth Newbury‐Ecob, Gareth Cross, Iain Fenton, J. A. Raeburn, I D Young, J. David Brook	1994	60
11	Manifesting heterozygosity in Norrie's disease? British Journal of Ophthalmology ·Geoffrey Woodruff, Ruth Newbury‐Ecob, Malahayati Bintang, I D Young	1993	6
12	Down's syndrome and fragile‐X syndrome in a single patient Journal of Intellectual Disability Research ·R. A. Collacott, Drew Duckett, Solomon Baah, Jill S. Warrington, I D Young	1990	7
13	Ocular findings in Angelman's (Happy Puppet) syndrome Ophthalmic Paediatrics and Genetics ·NFN Abdul, Alistair R. Fielder, I D Young, 贺百林	1990	20
14	Prenatal diagnosis of trisomy for the distal two‐thirds of the long arm of chromosome 14 (q21→qter) Prenatal Diagnosis ·Drew Duckett, E. Roberts, Ibrahim-Lenhardt, I D Young	1990	2
15	A recombinant X chromosome in a short statured girl resulting from a maternal pericentric inversion Human Genetics ·Drew Duckett, I D Young	1988	8
16	The Coffin-Lowry syndrome. Journal of Medical Genetics ·I D Young	1988	63
17	Osteogenesis imperfecta type IIA: evidence for dominant inheritance. Journal of Medical Genetics ·I D Young, Elizabeth M. Thompson, C. Michael Hall, Marcus Pembrey	1987	37
18	Distal symphalangism with involvement of the thumbs and great toes Clinical Genetics ·Marina Luciana Abreu de Melo, 斉比嘉, I D Young	1987	5
19	A patient with median cleft face anomaly and bilateral goldenhar anomaly American Journal of Medical Genetics ·Maria A. Musarella, I D Young, John M. Opitz, James F. Reynolds	1986	18
20	Microphthalmos in a family Ophthalmic Paediatrics and Genetics ·Isabelle Russell‐Eggitt, A R Fielder, Pål Nordby, I D Young	1985	6

About I D Young

I D Young is a scholar working on Developmental Biology, Genetics, Pediatrics, Perinatology and Child Health, Rheumatology and Genetics, having authored 79 papers that have together received 3.6k indexed citations. Recurring topics across this work include Connective tissue disorders research (8 papers), Congenital heart defects research (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers), Sexual Differentiation and Disorders (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and BRCA gene mutations in cancer (4 papers). The work is most often cited by research in Genetics (2.1k citations), Reproductive Medicine (332 citations), Developmental Biology (77 citations), Rheumatology (427 citations) and Molecular Biology (1.9k citations). I D Young has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include P.S. Harper, J. David Brook, Silvana Guioli, Sahar Mansour, M. Dominguez-Steglich, Cheni Kwok, Jamie W. Foster, Peter N. Goodfellow, Alan J. Schafer and Milena Stevanović. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, Journal of Intellectual Disability Research, Developmental Medicine & Child Neurology and The Lancet.

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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