Alice S. Brooks

2.8k total citations
29 papers, 595 citations indexed

About

Alice S. Brooks is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Alice S. Brooks has authored 29 papers receiving a total of 595 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 15 papers in Molecular Biology and 6 papers in Surgery. Recurrent topics in Alice S. Brooks's work include Genomics and Rare Diseases (8 papers), Genetic Syndromes and Imprinting (5 papers) and Epigenetics and DNA Methylation (5 papers). Alice S. Brooks is often cited by papers focused on Genomics and Rare Diseases (8 papers), Genetic Syndromes and Imprinting (5 papers) and Epigenetics and DNA Methylation (5 papers). Alice S. Brooks collaborates with scholars based in Netherlands, United States and United Kingdom. Alice S. Brooks's co-authors include Martinus F. Niermeijer, Patrick J. Willems, Jeannette Hoogeboom, Marja W. Wessels, Dick Tibboel, Karen Bindels‐de Heus, Marie‐Claire Y. de Wit, Ewout J. Hoorn, I.F.M. de Coo and Mahdi Salih and has published in prestigious journals such as Journal of the American Society of Nephrology, Genetics in Medicine and European Journal of Human Genetics.

In The Last Decade

Alice S. Brooks

28 papers receiving 586 citations

Peers

Countries citing papers authored by Alice S. Brooks

Since Specialization

Citations

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

Fields of papers citing papers by Alice S. Brooks

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alice S. Brooks. 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 Alice S. Brooks. The network helps show where Alice S. Brooks may publish in the future.

Co-authorship network of co-authors of Alice S. Brooks

This figure shows the co-authorship network connecting the top 25 collaborators of Alice S. Brooks. A scholar is included among the top collaborators of Alice S. Brooks based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Alice S. Brooks. Alice S. Brooks is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Characterization of HMGA2 variants expands the spectrum of Silver-Russell syndrome 2024 ·JCI Insight ·Avinaash Maharaj, (unknown), Thatchawan Thanasupawat, Sjoerd D. Joustra, Barbara L. Triggs‐Raine, Masanobu Fujimoto, Sarina G. Kant, (unknown), (unknown), Alice S. Brooks, Gabriel A. Aguirre, (unknown), (unknown), Ahmed Massoud, Hermine A. van Duyvenvoorde, Christiaan de Bruin, Vivian Hwa, Thomas Klonisch, Sabine Hombach‐Klonisch, Helen L. Storr	3
2	Multidisciplinary interaction and MCD gene discovery. The perspective of the clinical geneticist 2021 ·European Journal of Paediatric Neurology ·Grazia M.S. Mancini, Daphne J. Smits, (unknown), Rachel Schot, Marie‐Claire Y. de Wit, Maarten H. Lequin, Marjolein H. G. Dremmen, Alice S. Brooks, Tjakko J. van Ham, Frans W. Verheijen, Maarten Fornerod, William B. Dobyns, Martina Wilke	1
3	A novel UBE3A sequence variant identified in eight related individuals with neurodevelopmental delay, results in a phenotype which does not match the clinical criteria of Angelman syndrome 2020 ·Molecular Genetics & Genomic Medicine ·(unknown), (unknown), (unknown), Hennie T. Brüggenwirth, Ineke van der Burgt, Helger G. Yntema, (unknown), Alice S. Brooks, Ype Elgersma, Ben Distel, M. J. Valstar	11
4	Clinical aspects of a large group of adults with Angelman syndrome 2020 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), Hennie T. Brüggenwirth, Marion Koopmans, Alice S. Brooks, Ype Elgersma, Dederieke A. M. Festen, M. J. Valstar	14
5	An overview of health issues and development in a large clinical cohort of children with Angelman syndrome 2019 ·American Journal of Medical Genetics Part A ·Karen Bindels‐de Heus, Sabine E. Mous, (unknown), (unknown), (unknown), André B. Rietman, Leontine W. ten Hoopen, Alice S. Brooks, Ype Elgersma, Henriëtte A. Moll, Marie‐Claire Y. de Wit	53
6	Biallelic sequence variants in INTS1 in patients with developmental delays, cataracts, and craniofacial anomalies 2019 ·European Journal of Human Genetics ·(unknown), (unknown), Rhonda E. Schnur, Alice S. Brooks, Laura Baker, (unknown), Ryan E. Lamont, Karen W. Gripp, Dina Schneidman‐Duhovny, A. Micheil Innes, Grazia M.S. Mancini, Anne Slavotinek	26
7	Diagnosing Alport Syndrome: Lessons from the Pediatric Ward 2018 ·The Nephron journals/Nephron journals ·Paul De Vos, Robert Zietse, Michel van Geel, Alice S. Brooks, Karlien Cransberg	9
8	Postzygotic telomere capture causes segmental UPD, duplication and deletion of chromosome 8p in a patient with intellectual disability and obesity 2017 ·European Journal of Medical Genetics ·Jeroen Knijnenburg, (unknown), (unknown), Rianne Oostenbrink, Bert H.J. Eussen, Annelies de Klein, Alice S. Brooks, Laura J. C. M. van Zutven	5
9	JS-X syndrome: A multiple congenital malformation with vocal cord paralysis, ear deformity, hearing loss, shoulder musculature underdevelopment, and X-linked recessive inheritance 2015 ·International Journal of Pediatric Otorhinolaryngology ·L.J. Hoeve, Alice S. Brooks, Liesbeth S. Smit	4
10	Germline activating AKT3 mutation associated with megalencephaly, polymicrogyria, epilepsy and hypoglycemia 2014 ·Molecular Genetics and Metabolism ·Mark Nellist, Rachel Schot, Marianne Hoogeveen‐Westerveld, Rinze F. Neuteboom, Elles van der Louw, Maarten H. Lequin, Karen Bindels‐de Heus, Barbara Sibbles, I.F.M. de Coo, Alice S. Brooks, Grazia M.S. Mancini	36
11	Clinical and mutational characteristics of spinal muscular atrophy with respiratory distress type 1 in the Netherlands 2013 ·Neuromuscular Disorders ·(unknown), Aad Verrips, Bwee Tien Poll‐The, Jan-Maarten Cobben, I. Snoeck, I.F.M. de Coo, Alice S. Brooks, Saskia Bulk, R. H. J. M. Gooskens, (unknown), Corien C. Verschuuren‐Bemelmans, Richard J. Sinke, Marjolein Visser, Henny H. Lemmink	10
12	Congenital short bowel syndrome as the presenting symptom in male patients with FLNA mutations 2012 ·Genetics in Medicine ·(unknown), Yunia Sribudiani, Joanne Verheij, Matthew Carroll, Edward V. O’Loughlin, Chien-Huan Chen, Alice S. Brooks, M. Kathryn Liszewski, John P. Atkinson, Robert M.W. Hofstra	30
13	Incidental finding of alpha‐methylacyl‐CoA racemase deficiency in a patient with oculocutaneous albinism type 4 2012 ·American Journal of Medical Genetics Part A ·Judith M.A. Verhagen, J. G. M. Huijmans, Monique Williams, (unknown), Arthur A. Bergen, Carine Wouters, Alice S. Brooks	10
14	Functional characterization of the TSC2 c.3598C>T (p.R1200W) missense mutation that co‐segregates with tuberous sclerosis complex in mildly affected kindreds 2011 ·Clinical Genetics ·Marjolein Wentink, Mark Nellist, Marianne Hoogeveen‐Westerveld, Bernard A. Zonnenberg, (unknown), Ton van Essen, (unknown), Geoffrey Woods, Petra E. Cohn‐Hokke, Wim Brussel, Eric Smeets, Alice S. Brooks, Dicky Halley, Ans van den Ouweland, Anneke Maat‐Kievit	24
15	Beare-Stevenson Syndrome: Two Dutch Patients With Cerebral Abnormalities 2011 ·Pediatric Neurology ·Daniela Q.C.M. Barge‐Schaapveld, Alice S. Brooks, Maarten H. Lequin, (unknown), R. Jeroen Vermeulen, Jan Maarten Cobben	10
16	Absence epilepsy and periventricular nodular heterotopia 2010 ·Seizure ·Marie‐Claire Y. de Wit, H.M. Schippers, I.F.M. de Coo, W. F. M. Arts, Maarten H. Lequin, Alice S. Brooks, Gerhard H. Visser, Grazia M.S. Mancini	8
17	Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells 2009 ·European Journal of Human Genetics ·Jet Bliek, Mariëlle Alders, Saskia M. Maas, Roelof‐Jan Oostra, Deborah Mackay, K. Lip, (unknown), Alice S. Brooks, (unknown), A. Westerveld, N. J. Leschot, Marcel M. A. M. Mannens	74
18	Early diagnosis of Wolf–Hirschhorn syndrome triggered by a life‐threatening event: Congenital diaphragmatic hernia 2004 ·American Journal of Medical Genetics Part A ·M. F. van Dooren, Alice S. Brooks, A. Jeannette M. Hoogeboom, Thelma L. van den Hoonaard, Jan Klein, Carine Wouters, Dick Tibboel	20
19	Kabuki syndrome: a review study of three hundred patients 2002 ·Clinical Dysmorphology ·Marja W. Wessels, Alice S. Brooks, Jeannette Hoogeboom, Martinus F. Niermeijer, Patrick J. Willems	83
20	Unexpected life-threatening complications in Kabuki syndrome 2000 ·American Journal of Medical Genetics ·Mieke M. van Haelst, Alice S. Brooks, Jeannette Hoogeboom, Marja W. Wessels, Dick Tibboel, Johan C. de Jongste, Jan C. den Hollander, Jacoba J. Bongers‐Schokking, Martinus F. Niermeijer, Patrick J. Willems	25

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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