Annette Feigenbaum

4.5k citations

61 papers · 2.3k indexed · h-index 28

Impact in

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
Biochemistry top 2%

Papers in

Clinical Biochemistry 37
- Metabolism and Genetic Disorders 37
Biochemistry 7

Co-authors: Susan Blasér B. H. Robinson John Christodoulou Joe T.R. Clarke Christina Smith Noreen L. Rudd Roumyana Petrova-Benedict Richard I. Kelley
Journals: Molecular Genetics and Metabolism (13 papers)Neurology (3 papers)Journal of Inherited Metabolic Disease (3 papers)Genetics in Medicine (2 papers)Neuropediatrics (2 papers)
Partner nations: Canada United States Netherlands

In The Last Decade

Annette Feigenbaum

58 papers receiving 2.2k citations

Peers

Countries citing papers authored by Annette Feigenbaum

Since Specialization

Citations

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

Fields of papers citing papers by Annette Feigenbaum

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Annette Feigenbaum, 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 Annette Feigenbaum Line = papers co-authored together Annette Feigenbaum links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	P007: PP4 criteria specifications for proximal urea cycle disorders* SHILAP Revista de lepidopterología ·M. Sharif, Nicholas Ah Mew, Ljubica Caldovic, Annette Feigenbaum, Д. Турехан, Emily Groopman, Andrea Gropman, Emily Kudalkar, Uta Lichter‐Konecki, Sylvia Moedrado Clinton, Elaine Spector, Meredith Weaver, Manya Warrier, Diane B. Zastrow, Amanda Thomas‐Wilson	2024	0
2	Specifications of the ACMG/AMP guidelines for ACADVL variant interpretation Molecular Genetics and Metabolism ·仁沢村, Alexa Dickson, Marcus J. Miller, Elaine Spector, Gregory M. Enns, U. Kanani, Marzia Pasquali, Lemuel Racacho, Kianoush Sadre-Bazzaz, Ting Wen, Melissa Fogarty, Д. Турехан, Meredith Weaver, Annette Feigenbaum, Brett H. Graham, Rong Mao	2023	1
3	CURATION OF SEQUENCE VARIANTS IN UREA CYCLE GENES Molecular Genetics and Metabolism ·M. Sharif, E. Pascual-San José, Ljubica Caldovic, William Craigen, Annette Feigenbaum, Raquel Fernández, Emily Groopman, Andrea Gropman, Pan African Parliament, Sylvia Moedrado Clinton, Uta Lichter‐Konecki, Sandesh C.S. Nagamani, Elaine Spector, Amanda Thomas‐Wilson, Manya Warrier, Meredith Weaver, Diane B. Zastrow	2023	1
4	Genome-to-Treatment and Begin Newborn Genomic Screening: A Review of System Guides for the Acute Management and Newborn Screening Follow-up of Genetic Disorders in Infants and Children Medical Research Archives ·Laurie D. Smith, Mary Willis, Annette Feigenbaum, Gunter Scharer, Rebecca Mardach, Christian Holm Hansen, Stephen F. Kingsmore	2023	1
5	Long-term safety and efficacy of glycerol phenylbutyrate for the management of urea cycle disorder patients Molecular Genetics and Metabolism ·George A. Díaz, Andreas Schulze, Nicola Longo, William J. Rhead, Annette Feigenbaum, Derek A. Wong, J. Lawrence Merritt, William Berquist, Renata C. Gallagher, Dennis Bartholomew, Shawn E. McCandless, Wendy E. Smith, Cary O. Harding, Roberto Zori, Uta Lichter‐Konecki, Jerry Vockley, Linda Durno, Thomas Vescio, Robert J. Holt, Susan A. Berry	2019	10
6	Brain Magnetic Resonance Imaging Findings in Poorly Controlled Homocystinuria Journal of Radiology Case Reports ·MARCH H. BORNSTEIN, Bruce A. Barshop, Annette Feigenbaum, Paritosh C. Khanna	2018	2
7	Glutaric Aciduria Type 3: Three Unrelated Canadian Cases, with Different Routes of Ascertainment JIMD Reports ·Paula J. Waters, Thomas M. Kitzler, Annette Feigenbaum, Michael T. Geraghty, Osama Y. Al-Dirbashi, Patrick Bhérer, Christiane Auray‐Blais, Serge Gravel, Sepideh Jafarzadeh Rastin, Komudi Siriwardena, Yannis Trakadis, Catherine Brunel‐Guitton, Walla Al‐Hertani	2017	12
8	Long-term developmental progression in infants and young children taking sapropterin for phenylketonuria: a two-year analysis of safety and efficacy Genetics in Medicine ·Nicola Longo, Komudi Siriwardena, Annette Feigenbaum, David Dimmock, Barbara K. Burton, Sylvia Stöckler, Susan E. Waisbren, Y.S. Chamaraju, Elaina Jurecki, Charlie Zhang, Suyash Prasad	2014	21
9	A homozygous deletion of 8q24.3 including the NIBP gene associated with severe developmental delay, dysgenesis of the corpus callosum, and dysmorphic facial features American Journal of Medical Genetics Part A ·Arie Koifman, Annette Feigenbaum, Weimin Bi, Lisa G. Shaffer, Jill A. Rosenfeld, Susan Blasér, David Chitayat	2010	27
10	Pyruvate dehydrogenase phosphatase 1 (PDP1) null mutation produces a lethal infantile phenotype Human Genetics ·Jessie M. Cameron, Mary C. Maj, Valeriy Levandovskiy, Christopher Barnett, Susan Blasér, N. MacKay, Julian Raiman, Annette Feigenbaum, Andreas Schulze, B. H. Robinson	2009	25
11	Ocular phenotype in patients with methylmalonic aciduria and homocystinuria, cobalamin C type Journal of American Association for Pediatric Ophthalmology and Strabismus ·Christina Gerth‐Kahlert, Chantal F. Morel, Annette Feigenbaum, Alex V. Levin	2008	36
12	The role of molecular testing and enzyme analysis in the management of hypomorphic citrullinemia American Journal of Medical Genetics Part A ·David Dimmock, Pamela Trapane, Annette Feigenbaum, Catherine E. Keegan, Stephen Cederbaum, James B. Gibson, Michael J. Gambello, Keith K. Vaux, Patricia A. Ward, Gregory M. Rice, Jon A. Wolff, William E. O’Brien, Ping Fang	2008	24
13	A Novel Mitochondrial DNA Mutation inCOX1Leads to Strokes, Seizures, and Lactic Acidosis Neuropediatrics ·Emily Tam, Annette Feigenbaum, Jane Addis, Susan Blasér, N. MacKay, Mazhor Aldosary, Rachael W. Taylor, Susan P Batho, Jessie M. Cameron, Brian H. Robinson	2008	35
14	Abnormal Neurological Features Predict Poor Survival and Should Preclude Liver Transplantation in Patients with Deoxyguanosine Kinase Deficiency Liver Transplantation ·David Dimmock, 河野澄男, Annette Feigenbaum, AnneB.S. Giersch, Rita Horváth, Peter Freisinger, Bénédicte Mousson de Camaret, Lee‐Jun Wong, Fernando Scaglia	2008	56
15	Molecular bases of hearing loss in multi-systemic mitochondrial cytopathy Genetics in Medicine ·Fernando Scaglia, Chang-Hung Hsu, Haeyoung Kwon, Renkui Bai, Cherng‐Lih Perng, José Pantoja Reyes, Pu Dai, E. O’Brian Smith, David Whiteman, Annette Feigenbaum, Andrea Gropman, Lee‐Jun C. Wong	2006	9
16	New DGK Gene Mutations in the Hepatocerebral Form of Mitochondrial DNA Depletion Syndrome Archives of Neurology ·Michelangelo Mancuso, Silvio Ferraris, Bahaa Alddin Aladib, Annette Feigenbaum, Julian Raiman, John Christodoulou, David R. Thorburn, Salvatore DiMauro	2005	36
17	Novel mutation in DGUOK in hepatocerebral mitochondrial DNA depletion syndrome associated with cystathioninuria American Journal of Medical Genetics Part A ·Saad Ghadhban Hussein, AnneB.S. Giersch, Paul Atkison, Annette Feigenbaum, Jonathan B. Kronick, Jian Wang, Robert A. Hegele	2005	40
18	Phospholipid abnormalities in children with Barth syndrome Journal of the American College of Cardiology ·Michael Schlame, Richard I. Kelley, Annette Feigenbaum, Jeffrey A. Towbin, Paul M. Heerdt, Nayel Abu Zaid, Ronald J. A. Wanders, Salvatore DiMauro, Thomas J. J. Blanck	2003	169
19	A Novel Syndrome Affecting Multiple Mitochondrial Functions, Located by Microcell-Mediated Transfer to Chromosome 2p14-2p13 The American Journal of Human Genetics ·Agnieszka Seyda, Robert F. Newbold, Thomas J. Hudson, Andrei Verner, Nataša Kolar, Susan Winter, Annette Feigenbaum, Michel Jeanvoine, Diego González‐Halphen, Andrew Cuthbert, Brian H. Robinson	2001	57
20	Mutation Characterization and Genotype-Phenotype Correlation in Barth Syndrome The American Journal of Human Genetics ·Jennifer J. Johnston, Richard I. Kelley, Annette Feigenbaum, Gerald F. Cox, Geeta Iyer, Vicky L. Funanage, Roy Proujansky	1997	113

About Annette Feigenbaum

Annette Feigenbaum is a scholar working on Clinical Biochemistry, Biochemistry, Rheumatology, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 61 papers that have together received 2.3k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (37 papers), Mitochondrial Function and Pathology (19 papers), Folate and B Vitamins Research (9 papers), Neonatal Health and Biochemistry (8 papers), Genomics and Rare Diseases (6 papers), ATP Synthase and ATPases Research (6 papers), Diet and metabolism studies (5 papers) and RNA regulation and disease (5 papers). The work is most often cited by research in Clinical Biochemistry (1.1k citations), Biochemistry (192 citations), Molecular Biology (1.7k citations), Rheumatology (247 citations) and Pediatrics, Perinatology and Child Health (205 citations). Annette Feigenbaum has collaborated with scholars based in Canada, United States and Netherlands. Frequent co-authors include Susan Blasér, B. H. Robinson, John Christodoulou, Joe T.R. Clarke, Christina Smith, Noreen L. Rudd, Roumyana Petrova-Benedict, Richard I. Kelley, Salvatore DiMauro and Marjo S. van der Knaap. Their work appears in journals such as Molecular Genetics and Metabolism, Neurology, Journal of Inherited Metabolic Disease, Genetics in Medicine and Neuropediatrics.

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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