Daniel Kelberman

3.5k citations

43 papers · 2.2k indexed · h-index 28

Impact in

Endocrinology, Diabetes and Metabolism top 2%
- Growth Hormone and Insulin-like Growth Factors
- Pituitary Gland Disorders and Treatments
Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Ocular Disorders and Treatments
- Congenital Ear and Nasal Anomalies
- Genetic Syndromes and Imprinting

Papers in ⓘ

Genetics 27
- Ocular Disorders and Treatments 9
- Congenital Ear and Nasal Anomalies 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
- Genetic Syndromes and Imprinting 4
- Craniofacial Disorders and Treatments 4
Endocrinology, Diabetes and Metabolism 13
- Growth Hormone and Insulin-like Growth Factors 11

Co-authors: Mehul Dattani (24 shared papers)Karine Rizzoti (2 shared papers)Iain C. A. F. Robinson (2 shared papers)Robin Lovell‐Badge (2 shared papers)Juan Pedro Martı́nez-Barberá (6 shared papers)Steve E. Humphries (5 shared papers)Jane C. Sowden (7 shared papers)John C. Achermann (3 shared papers)
Journals: The Journal of Clinical Endocrinology & Metabolism (6 papers)Human Molecular Genetics (3 papers)Human Mutation (3 papers)Clinical Endocrinology (2 papers)Hormone Research in Paediatrics (2 papers)
Partner nations: United Kingdom United States France

In The Last Decade

Daniel Kelberman

42 papers receiving 2.1k citations

Peers

Countries citing papers authored by Daniel Kelberman

Since Specialization

Citations

This map shows the geographic impact of Daniel Kelberman'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 Daniel Kelberman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel Kelberman more than expected).

Fields of papers citing papers by Daniel Kelberman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniel Kelberman. 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 Daniel Kelberman. The network helps show where Daniel Kelberman may publish in the future.

Co-authors

The 25 scholars most cited alongside Daniel Kelberman, 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 Daniel Kelberman Line = papers co-authored together Daniel Kelberman 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 43 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Genetic Regulation of Pituitary Gland Development in Human and Mouse Endocrine Reviews ·Daniel Kelberman, Karine Rizzoti, Robin Lovell‐Badge, Iain C. A. F. Robinson, Mehul Dattani	2009	294
2	Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans Journal of Clinical Investigation ·Daniel Kelberman	2006	242
3	Heterozygous Missense Mutations in Steroidogenic Factor 1 (SF1/Ad4BP, NR5A1) Are Associated with 46,XY Disorders of Sex Development with Normal Adrenal Function The Journal of Clinical Endocrinology & Metabolism ·Lin Lin, Pascal Philibert, Bruno Ferraz‐de‐Souza, Daniel Kelberman, Tessa Homfray, Assunta Albanese, Veruska Molini, Neil J. Sebire, Silvia Einaudi, Gerard S. Conway, Ieuan A. Hughes, J. Larry Jameson, Charles Sultan, Mehul Dattani, John C. Achermann	2007	150
4	SOX2 Plays a Critical Role in the Pituitary, Forebrain, and Eye during Human Embryonic Development The Journal of Clinical Endocrinology & Metabolism ·Daniel Kelberman, Sandra C. de Castro, Shuwen Huang, John A. Crolla, Rodger Palmer, John W. Gregory, David Taylor, Luciano Cavallo, Maria Felicia Faienza, Rita Fischetto, John C. Achermann, Juan Pedro Martı́nez-Barberá, Karine Rizzoti, Robin Lovell‐Badge, Iain C. A. F. Robinson, Dianne Gerrelli, Mehul Dattani	2008	115
5	HESX1Mutations Are an Uncommon Cause of Septooptic Dysplasia and Hypopituitarism The Journal of Clinical Endocrinology & Metabolism ·David McNay, James Turton, Daniel Kelberman, Kathryn Woods‐Townsend, Raja Brauner, Anastasios Papadimitriou, Eberhard Keller, Alexandra Keller, Nele Haufs, Heiko Krude, Stephen M. Shalet, Mehul Dattani	2006	108
6	Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome Human Genetics ·Daniel Kelberman, Jess Tyson, David Chandler, Aideen McInerney‐Leo, Jennie Slee, Darren L. Albert, A. Aymat, Marissa Botma, Mary Calvert, Jack Goldblatt, Eric Haan, Nigel G. Laing, Jennifer I. Lim, S Malcolm, Steven R. Singer, R M Winter, Maria Bitner‐Glindzicz	2001	92
7	CD19+CD24hiCD38hi B Cells Are Expanded in Juvenile Dermatomyositis and Exhibit a Pro-Inflammatory Phenotype After Activation Through Toll-Like Receptor 7 and Interferon-α Frontiers in Immunology ·Christopher Piper, Meredyth Wilkinson, Claire T. Deakin, Georg Otto, Stefanie Dowle, Chantal L. Duurland, Stuart Adams, Emiliano Marasco, Elizabeth C. Rosser, Anna Radziszewska, Rita Carsetti, Yiannis Ioannou, Philip L. Beales, Daniel Kelberman, David Isenberg, Claudia Mauri, Kiran Nistala, Lucy R. Wedderburn	2018	75
8	Lack of the murine homeobox geneHesx1leads to a posterior transformation of the anterior forebrain Development ·Cynthia L. Andoniadou, Massimo Signore, Ezat Sajedi, Carles Gaston‐Massuet, Daniel Kelberman, Alan J. Burns, Nobue Itasaki, Mehul Dattani, Juan Pedro Martı́nez-Barberá	2007	69
9	Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss Human Molecular Genetics ·A Rajab, Daniel Kelberman, Sandra C. de Castro, Heike Biebermann, Hiba Arshad Shaikh, Karma Pearce, C. M. Hall, Guftar Shaikh, Dianne Gerrelli, Annette Grueters, Heiko Krude, Mehul Dattani	2008	65
10	Hypothalamic and pituitary development: novel insights into the aetiology European Journal of Endocrinology ·Daniel Kelberman, Mehul Dattani	2007	61
11	Septo-Optic Dysplasia – Novel Insights into the Aetiology Hormone Research in Paediatrics ·Daniel Kelberman, Mehul Dattani	2008	58
12	Genetics of septo-optic dysplasia Pituitary ·Daniel Kelberman, Mehul Dattani	2007	58
13	ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous Human Molecular Genetics ·Lev Prasov, Tehmina Masud, Shagufta Khaliq, S. Qasim Mehdi, Aiysha Abid, Edward R. Oliver, Eduardo Silva, Amy Lewanda, Michael C. Brodsky, Mark Borchert, Daniel Kelberman, Jane C. Sowden, Mehul Dattani, Tom Glaser	2012	51
14	Novel IL-6 haplotypes and disease association Genes and Immunity ·M Fife, Emma Ogilvie, Daniel Kelberman, Jane Samuel, Ana Gutiérrez, Steve E. Humphries, Patricia Woo	2005	47
15	Hypopituitarism Oddities: Congenital Causes Hormone Research in Paediatrics ·Daniel Kelberman, Mehul Dattani	2007	46
16	The role of transcription factors implicated in anterior pituitary development in the aetiology of congenital hypopituitarism Annals of Medicine ·Daniel Kelberman, Mehul Dattani	2006	44
17	Effect of Interleukin-6 promoter polymorphisms in survivors of myocardial infarction and matched controls in the North and South of Europe Thrombosis and Haemostasis ·Daniel Kelberman, Emma Hawe, L A Luong, Vidya Mohamed‐Ali, Pia Lundman, Per Tornvall, M. F. Aillaud, I. Juhan‐Vague, John Yudkin, Maurizio Margaglione, Giovanni Di Minno, Elena Tremoli, Steve E. Humphries, (unknown)	2004	40
18	Impaired EIF2S3 function associated with a novel phenotype of X-linked hypopituitarism with glucose dysregulation EBioMedicine ·Louise Gregory, Carolina Baeta Neves Duarte Ferreira, Sara K. Young, Hywel Williams, Magdaléna Harakaľová, Gijs van Haaften, Sofia Rahman, Carles Gaston‐Massuet, Daniel Kelberman, GOSgene, Waseem Qasim, Sally A. Camper, Thomas Dever, Pratik Shah, Iain C.A.F. Robinson, Mehul Dattani	2019	40
19	Mutation of SALL2 causes recessive ocular coloboma in humans and mice Human Molecular Genetics ·Daniel Kelberman, Lily Islam, Jörn Lakowski, Chiara Bacchelli, Estelle Chanudet, Francesco Lescai, AmitP Patel, Elia Stupka, A. Buck, Stephan Wolf, Philip L. Beales, Thomas S. Jacques, Maria Bitner‐Glindzicz, Alki Liasis, Ordan J. Lehmann, Jürgen Kohlhase, Ken K. Nischal, Jane C. Sowden	2014	37
20	Molecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD) Clinical Endocrinology ·Daniel Kelberman, James Turton, (unknown), A. Mehta, Mona Alkhawari, James Greening, Peter G.F. Swift, Timo Otonkoski, Simon J. Rhodes, Mehul Dattani	2008	34

About Daniel Kelberman

Daniel Kelberman is a scholar working on Genetics, Endocrinology, Diabetes and Metabolism, Genetics, Molecular Biology and Immunology, having authored 43 papers that have together received 2.2k indexed citations. Recurring topics across this work include Growth Hormone and Insulin-like Growth Factors (11 papers), Ocular Disorders and Treatments (9 papers), Hedgehog Signaling Pathway Studies (8 papers), Congenital Ear and Nasal Anomalies (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Genetic Syndromes and Imprinting (4 papers), Congenital heart defects research (4 papers) and Craniofacial Disorders and Treatments (4 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (717 citations), Genetics (967 citations), Genetics (219 citations), Reproductive Medicine (150 citations) and Molecular Biology (1.1k citations). Daniel Kelberman has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Mehul Dattani, Karine Rizzoti, Iain C. A. F. Robinson, Robin Lovell‐Badge, Juan Pedro Martı́nez-Barberá, Steve E. Humphries, Jane C. Sowden, John C. Achermann, Patricia Woo and Kyriaki S. Alatzoglou. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, Human Molecular Genetics, Human Mutation, Clinical Endocrinology and Hormone Research in Paediatrics.

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