Uta Lichter‐Konecki

2.3k citations

47 papers · 1.3k indexed · h-index 23

Impact in

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
Rheumatology top 2%
- Folate and B Vitamins Research

Papers in

Clinical Biochemistry 39
- Metabolism and Genetic Disorders 39
Biochemistry 9
- Amino Acid Enzymes and Metabolism 9

Co-authors: David Konecki Savio L.C. Woo Friedrich K. Trefz Randy C. Eisensmith Christine Brown Jerry Vockley Magdalena Schlotter Alexei A. Goltsov
Journals: Human Genetics (7 papers)Molecular Genetics and Metabolism (4 papers)Journal of Inherited Metabolic Disease (3 papers)The Journal of Pediatrics (2 papers)Biochemistry (2 papers)
Partner nations: United States Germany Italy

In The Last Decade

Uta Lichter‐Konecki

44 papers receiving 1.3k citations

Peers

Countries citing papers authored by Uta Lichter‐Konecki

Since Specialization

Citations

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

Fields of papers citing papers by Uta Lichter‐Konecki

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Uta Lichter‐Konecki. 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 Uta Lichter‐Konecki. The network helps show where Uta Lichter‐Konecki may publish in the future.

Co-authors

The 25 scholars most cited alongside Uta Lichter‐Konecki, 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 Uta Lichter‐Konecki Line = papers co-authored together Uta Lichter‐Konecki 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 ·Kara Simpson, Nicholas Ah Mew, Ljubica Caldovic, Annette Feigenbaum, Raquel Fernandez, Emily Groopman, Andrea Gropman, Emily Kudalkar, Uta Lichter‐Konecki, McKenna Kyriss, Elaine Spector, Meredith Weaver, Manya Warrier, Diane B. Zastrow, Amanda Thomas‐Wilson	2024	0
2	Late diagnosis of the X-linked MCT8 deficiency (Allan–Herndon–Dudley syndrome) in a teenage girl with primary ovarian insufficiency Journal of Pediatric Endocrinology and Metabolism ·Swetha Sriram, Nabiha Shahid, Diana Mysliwiec D, Uta Lichter‐Konecki, Svetlana A. Yatsenko, Luigi Garibaldi	2024	1
3	CURATION OF SEQUENCE VARIANTS IN UREA CYCLE GENES Molecular Genetics and Metabolism ·Kara Simpson, Nicholas Ah. Mew, Ljubica Caldovic, William Craigen, Annette Feigenbaum, Raquel Fernández, Emily Groopman, Andrea Gropman, Emily Kudalker, McKenna Kyriss, Uta Lichter‐Konecki, Sandesh C.S. Nagamani, Elaine Spector, Amanda Thomas‐Wilson, Manya Warrier, Meredith Weaver, Diane B. Zastrow	2023	1
4	Multisite Retrospective Review of Outcomes in Renal Replacement Therapy for Neonates with Inborn Errors of Metabolism The Journal of Pediatrics ·Elizabeth G. Ames, Corey Powell, Rachel M. Engen, Donald J. Weaver, Asif Mansuri, Michelle N. Rheault, Keia Sanderson, Uta Lichter‐Konecki, Ankana Daga, Lindsay C. Burrage, Ayesha Ahmad, Scott E. Wenderfer, Kera E. Luckritz	2022	5
5	Consensus guidelines for management of hyperammonaemia in paediatric patients receiving continuous kidney replacement therapy Nature Reviews Nephrology ·Rupesh Raina, Jirair K. Bedoyan, Uta Lichter‐Konecki, Philippe Jouvet, Stefano Picca, Nicholas Ah Mew, Marcel Cerqueira César Machado, Ronith Chakraborty, Meghana Vemuganti, Manpreet Kaur Grewal, Timothy E. Bunchman, Sidharth Kumar Sethi, Vinod Krishnappa, Mignon McCulloch, Khalid Alhasan, Arvind Bagga, Rajit K. Basu, Franz Schaefer, Guido Filler, Bradley A. Warady	2020	44
6	Clinical, biochemical, mitochondrial, and metabolomic aspects of methylmalonate semialdehyde dehydrogenase deficiency: Report of a fifth case Molecular Genetics and Metabolism ·Steven F. Dobrowolski, Ahmad Alodaib, Anuradha Karunanidhi, Shrabini Basu, Meghan Holecko, Uta Lichter‐Konecki, Kirk L. Pappan, Jerry Vockley	2020	14
7	Inborn Errors of Metabolism with Cognitive Impairment Pediatric Clinics of North America ·Evgenia Sklirou, Uta Lichter‐Konecki	2018	8
8	Defects of the urea cycle Uta Lichter‐Konecki	2016	7
9	Phenylketonuria (PKU): A problem solved? SHILAP Revista de lepidopterología ·Christine Brown, Uta Lichter‐Konecki	2015	83
10	Menkes disease in affected females: The clinical disease spectrum American Journal of Medical Genetics Part A ·Patroula Smpokou, Monisha Samanta, Gerard T. Berry, Leah Hecht, Elizabeth C. Engle, Uta Lichter‐Konecki	2014	22
11	Two-Tier Approach to the Newborn Screening of Methylenetetrahydrofolate Reductase Deficiency and Other Remethylation Disorders with Tandem Mass Spectrometry The Journal of Pediatrics ·Silvia Tortorelli, Coleman Turgeon, James Lim, Steve Baumgart, D Day-Salvatore, José E. Abdenur, Jonathan A. Bernstein, Fred Lorey, Uta Lichter‐Konecki, Devin Oglesbee, Kimiyo Raymond, Dietrich Matern, Lisa A. Schimmenti, Piero Rinaldo, Dimitar K. Gavrilov	2010	25
12	The locus for autosomal dominant renal Fanconi Syndrome maps to the long arm of chromosome 15 Genetics in Medicine ·Uta Lichter‐Konecki, Karl W. Broman, Richard A. Dart, Edward B. Blau, David Konecki	2000	0
13	Expression patterns of murine lysosome-associated membrane protein 2 (Lamp-2) transcripts during morphogenesis Differentiation ·Uta Lichter‐Konecki, S E Moter, Bruce R. Krawisz, Magdalena Schlotter, Christine M. Hipke, David Konecki	1999	23
14	Relative frequency of IVS10nt546 mutation in a Portuguese phenylketonuric population Human Mutation ·Isabel Rivera, Paula Leandro, Uta Lichter‐Konecki, Isabel Tavares de Almeida, Maria Celeste Lechner	1997	1
15	Genotype-phenotype correlations in phenylketonuria Clinica Chimica Acta ·Friedrich K. Trefz, Peter Burgard, Thomas König, B. Goebel‐Schreiner, Uta Lichter‐Konecki, David Konecki, E. D. Schmidt, Hildgund Schmidt, Horst Bickel	1993	33
16	Structural characterization of the 5' regions of the human phenylalanine hydroxylase gene Biochemistry ·David Konecki, Yibin Wang, Friedrich K. Trefz, Uta Lichter‐Konecki, Savio L.C. Woo	1992	45
17	Molecular Basis of Phenotypic Heterogeneity in Phenylketonuria New England Journal of Medicine ·Yoshiyuki Okano, Randy C. Eisensmith, Flemming Güttler, Uta Lichter‐Konecki, David Konecki, Friedrich K. Trefz, M. Dasovich, Tao Wang, Karen Friis Henriksen, Hans C. Lou, Savio L.C. Woo	1991	206
18	The identification of two mis-sense mutations at the PAH gene locus in a Turkish patient with phenylketonuria Human Genetics ·David Konecki, Magdalena Schlotter, Friedrich K. Trefz, Uta Lichter‐Konecki	1991	16
19	RFLP-patterns in Japanese PKU families: new polymorphisms for the mutant phenylalanine hydroxylase gene Human Genetics ·FriedrichK. Trefz, Makoto Yoshino, Atsushi Nishiyori, Frank Aengeneyndt, Brigitte Schmidt-Mader, Uta Lichter‐Konecki, DavidS. Konecki	1990	11
20	Changes in the Eeg Background Activity of Children with Acute Lymphoblastic Leukemia During Cytotoxic Therapy Pediatric Hematology and Oncology ·Uta Lichter‐Konecki, C. Benninger, W. Brandeis, P. Matthis, D. Scheffner	1987	5

About Uta Lichter‐Konecki

Uta Lichter‐Konecki is a scholar working on Clinical Biochemistry, Biochemistry, Rheumatology, Cell Biology and Genetics, having authored 47 papers that have together received 1.3k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (39 papers), Folate and B Vitamins Research (16 papers), Biochemical and Molecular Research (12 papers), Amino Acid Enzymes and Metabolism (9 papers), Diet and metabolism studies (6 papers), Muscle metabolism and nutrition (5 papers), Metabolomics and Mass Spectrometry Studies (4 papers) and Neonatal Health and Biochemistry (4 papers). The work is most often cited by research in Clinical Biochemistry (969 citations), Rheumatology (388 citations), Biochemistry (179 citations), Molecular Biology (774 citations) and Physiology (260 citations). Uta Lichter‐Konecki has collaborated with scholars based in United States, Germany and Italy. Frequent co-authors include David Konecki, Savio L.C. Woo, Friedrich K. Trefz, Randy C. Eisensmith, Christine Brown, Jerry Vockley, Magdalena Schlotter, Alexei A. Goltsov, Yoshiyuki Okano and Karen Friis Henriksen. Their work appears in journals such as Human Genetics, Molecular Genetics and Metabolism, Journal of Inherited Metabolic Disease, The Journal of Pediatrics and Biochemistry.

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