L-H. Gu

423 citations

29 papers · 313 · h-index 9

Impact in

Genetics top 5%
- Hemoglobinopathies and Related Disorders
Hematology top 5%
- Iron Metabolism and Disorders
- Blood groups and transfusion

Papers in

Genetics 21
- Hemoglobinopathies and Related Disorders 21
Hematology 14
- Iron Metabolism and Disorders 10
- Blood groups and transfusion 8

Co-authors: F. Kutlar (4 shared papers)T. H. J. Huisman (5 shared papers)M. Ramachandran (4 shared papers)T. H. J. Huisman (11 shared papers)J. B. Wilson (5 shared papers)T. H. J. Huisman (6 shared papers)Raymond Li (1 shared paper)T. P. Molchanova (7 shared papers)
Journals: Blood (3 papers)Hemoglobin (23 papers)Annals of Oncology (1 paper)Gastroenterology (1 paper)PubMed (1 paper)
Partner nations: United States China Spain

In The Last Decade

L-H. Gu

28 papers receiving 301 citations

Peers

Countries citing papers authored by L-H. Gu

Since Specialization

Citations

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

Fields of papers citing papers by L-H. Gu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by L-H. Gu. 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 L-H. Gu. The network helps show where L-H. Gu may publish in the future.

Co-authors

The 25 scholars most cited alongside L-H. Gu, 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 L-H. Gu Line = papers co-authored together L-H. Gu 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 29 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Observations on the levels of Hb A2 in patients with different beta- thalassemia mutations and a delta chain variant Blood ·JF Codrington, Hsin-Yun Li, F. Kutlar, L-H. Gu, M. Ramachandran, T. H. J. Huisman	1990	58
2	Observations on the levels of Hb A2 in patients with different beta- thalassemia mutations and a delta chain variant Blood ·JF Codrington, Raymond Li, F. Kutlar, L-H. Gu, M. Ramachandran, T. H. J. Huisman	1990	46
3	Types of Thalassemia Among Patients Attending a Large University Clinic in Kuala Lumpur, Malaysia Hemoglobin ·Elizabeth George, H-J. Li, Y-J. Fei, A. L. Reese, E. Baysal, B. Cepreganova, J. B. Wilson, L-H. Gu, John Nechtman, T. A. Stoming, J-C. Liu, John Codrington, T. H. J. Huisman	1992	42
4	γ Chain Abnormalities and γ-Globin Gene Rearrangements in Newborn Babies of Various Populations Hemoglobin ·T. H. J. Huisman, F. Kutlar, L-H. Gu	1991	21
5	A Second Observation of the Fetal Methehoglobin Variant HB F-M-Fort Ripley or α₂^Gγ₂⁹²(F8)HIS→TYR Hemoglobin ·T. P. Molchanova, J. B. Wilson, L-H. Gu, Richard Hain, L. S. Chang, Annette Poon, T. H. J. Huisman	1992	18
6	[Studies on antibacterial constituents from Gerbera anandria (L.) Sch Bip. IV]. PubMed ·L-H. Gu, Li X, Yan Sq, Zhu Tr	1987	12
7	Hb Bab-Saaooun or α₂β₂48(CD7)Leu→pro, A Mildly Unstable Variant Found in an Arabian Boy from Tunisia Hemoglobin ·T. P. Molchanova, J. B. Wilson, L-H. Gu, Fethi Guémira, S. Fattoum, T. H. J. Huisman	1992	11
8	Oligopeptide transporter PEPT1 mRNA expression in human intestinal mucosa: Gut gradient, cellular localization and colonic upregulation in short bowel syndrome (SBS) Gastroenterology ·T. Ziegler, CF Estivariz, L-H. Gu, T.M. Wallace, EE Díaz, RR Pascal, JR Galloway, JN Wilcox, L Leader	1998	9
9	HB Coimbra or α₂β₂99(Gl)ASP→GLU, A Newly Discovered High Oxygen Affinity Variant Hemoglobin ·G. P. Tamagnini, Maria Letícia Ribeiro, Victor Valente, M. Ramachandran, J. B. Wilson, E. Baysal, L-H. Gu, T. H. J. Huisman	1991	9
10	A newly discovered frameshift at codons 120-121 (+A) of the beta gene is not associated with a dominant form of beta-thalassemia [letter] Blood ·P. Hopmeier, Walter Krugluger, L-H. Gu, Н.С. Сметанина, TH Huisman	1996	8
11	Hb Fannin-Lubbock in Five Spanish Families is Characterized by two Mutations: β111 GTC->CTC (VAL->LEU) AND β119 GGC->GAC (GLY->ASP) Hemoglobin ·W-B. Qin, D. D. Pobedimskaya, T. P. Molchanova, J. B. Wilson, L-H. Gu, J. M. De Pablos, T. H. J. Huisman	1994	7
12	HB F-Sacromonte or α₂G_γ259(E3)LYS→GLN Observed in a Spanish Newborn and His Mother Hemoglobin ·D. D. Pobedimskaya, T. P. Molchanova, L-H. Gu, M.A. Molina, J. M. De Pablos, T. H. J. Huisman	1993	7
13	HB Tigraye OR α₂β²79(EF3)ASP→HIS(GAC→CAC): A Hemoglobin Variant with Increased Oxygen Affinity Observed in an Ethiopian Male Hemoglobin ·Molchanova Tp, Postnikov YuV, L-H. Gu, (unknown), (unknown)	1993	7
14	A new Variant, Hb Muscat [α₂β₂32(B14)Leu→val] Observed in Association With Hb S in an Arabian Family Hemoglobin ·M. Ramachandran, L-H. Gu, J. B. Wilson, Michael N. Kitundu, Adekunle Adekile, J-C. Liu, Kathleen McKie, T. H. J. Huisman	1992	7
15	Hb Zengcg or α2β₂114(G16)Leu → Met Hemoglobin ·Dijana Plaseska‐Karanfilska, J. B. Wilson, L-H. Gu, F. Kutlar, T. H. J. Huisman, Y-T. Zeng, Mengqin Shen	1990	6
16	The^Gγ^TChain (^Gγ75 Thr; 136 Gly) In Hb F-Charlotte Is The Product Of An^Aγ Gene With A Limited Gene Conversion And That In Hb F-Waynesboro Of A Mutated^Gγ Gene Hemoglobin ·L-H. Gu, C. Öner, T. H. J. Huisman	1995	6
17	HB Madrid or α₂β₂115(G17)ALA→PRO in a Black Teenager Hemoglobin ·T. P. Molchanova, Yu. V. Postnikov, J. J. Wilson, B. B. Webber, L-H. Gu, H. Sabio, P. Waldron, T. H. J. Huisman	1993	5
18	Hb S-Hb Lufkin Dise in A Black Male Infant Hemoglobin ·L-H. Gu, J.Ye. Leonova, T. H. J. Huisman	1995	5
19	The Relative Levels of Different Types of β-mRNA and β-Globin in BFU-E Derived Colonies from Patients with β Chain Variants; Further Evidence for Somatic Mosaicism in the Hb Costa Rica Carrier [β77(EF1)HISÅG] Hemoglobin ·Н.С. Сметанина, L-H. Gu, Walter Rodríguez-Romero, EF Howard, T. H. J. Huisman	1996	4
20	Two Rare Hemoglobin Variants: Hb Pyrgos [β83(ef7)Gly->Asp] and Hb Legnano [α141(hc3)arg->leu] Found in Inner Mongolia, P.R. China Hemoglobin ·W-B. Qin, X-L. Yue, L-Y. Qin, T-L. Ju, J. B. Wilson, L-H. Gu, T. H. J. Huisman	1994	4

About L-H. Gu

L-H. Gu is a scholar working on Genetics, Hematology, Physiology, Cell Biology and Pediatrics, Perinatology and Child Health, having authored 29 papers that have together received 313 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (21 papers), Iron Metabolism and Disorders (10 papers), Blood groups and transfusion (8 papers), Hemoglobin structure and function (7 papers), Erythrocyte Function and Pathophysiology (7 papers), Neonatal Health and Biochemistry (3 papers), Vascular Tumors and Angiosarcomas (1 paper) and Cancer, Hypoxia, and Metabolism (1 paper). The work is most often cited by research in Genetics (251 citations), Hematology (193 citations), Pediatrics, Perinatology and Child Health (75 citations), Cell Biology (45 citations) and Physiology (44 citations). L-H. Gu has collaborated with scholars based in United States, China and Spain. Frequent co-authors include F. Kutlar, T. H. J. Huisman, M. Ramachandran, T. H. J. Huisman, J. B. Wilson, T. H. J. Huisman, Raymond Li, T. P. Molchanova, E. Baysal and A. L. Reese. Their work appears in journals such as Blood, Hemoglobin, Annals of Oncology, Gastroenterology and PubMed.

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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