L-H. Gu

423 total citations
29 papers, 313 citations indexed

About

L-H. Gu is a scholar working on Genetics, Hematology and Physiology. According to data from OpenAlex, L-H. Gu has authored 29 papers receiving a total of 313 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 14 papers in Hematology and 9 papers in Physiology. Recurrent topics in L-H. Gu's work include Hemoglobinopathies and Related Disorders (21 papers), Iron Metabolism and Disorders (10 papers) and Blood groups and transfusion (8 papers). L-H. Gu is often cited by papers focused on Hemoglobinopathies and Related Disorders (21 papers), Iron Metabolism and Disorders (10 papers) and Blood groups and transfusion (8 papers). L-H. Gu collaborates with scholars based in United States, China and Spain. L-H. Gu's co-authors include F. Kutlar, T. H. J. Huisman, M. Ramachandran, T. H. J. Huisman, J. B. Wilson, T. H. J. Huisman, T. P. Molchanova, Raymond Li, E. Baysal and John Codrington and has published in prestigious journals such as Blood, Gastroenterology and Annals of Oncology.

In The Last Decade

L-H. Gu

28 papers receiving 301 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
L-H. Gu United States	9	251	193	75	49	45	29	313
Peter Hawkins United States	8	98 0.4×	82 0.4×	33 0.4×	57 1.2×	15 0.3×	13	193
Nicole Bouver United States	10	458 1.8×	299 1.5×	182 2.4×	94 1.9×	102 2.3×	11	517
Houda Hamdi‐Rozé France	10	68 0.3×	72 0.4×	27 0.4×	107 2.2×	17 0.4×	14	228
V J Buckle United Kingdom	5	51 0.2×	58 0.3×	24 0.3×	219 4.5×	8 0.2×	5	334
Kristin Johnson United States	6	51 0.2×	32 0.2×	14 0.2×	89 1.8×	18 0.4×	10	158
Riffat Ahmed United States	5	154 0.6×	185 1.0×	4 0.1×	49 1.0×	14 0.3×	5	249
Paul Toran United States	5	195 0.8×	242 1.3×	3 0.0×	69 1.4×	8 0.2×	12	321
Mylène Béri‐Dexheimer France	6	34 0.1×	54 0.3×	18 0.2×	45 0.9×	2 0.0×	8	159
Chandran Ka France	9	146 0.6×	185 1.0×	6 0.1×	50 1.0×	2 0.0×	20	246
Andrei M. Vacaru United States	8	28 0.1×	18 0.1×	12 0.2×	121 2.5×	35 0.8×	16	196

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-authorship network of co-authors of L-H. Gu

This figure shows the co-authorship network connecting the top 25 collaborators of L-H. Gu. A scholar is included among the top collaborators of L-H. Gu 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 L-H. Gu. L-H. Gu 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

Fan, Zhengqiu, Tian Yang, L-H. Gu, et al.. (2023). 971P Effect of preoperative frailty on surgical outcomes following hepatic resection for elderly patients with hepatocellular carcinoma: A multicenter retrospective cohort study from China. Annals of Oncology. 34. S603–S603. 2 indexed citations

Molchanova, T. P., et al.. (1998). Historical Note: The β-Thalassemia Allele in the Noble Russian Family Lermontov is Identified as the ATG←ACG Change in the Initiation Codon. Hemoglobin. 22(3). 283–286. 3 indexed citations

Сметанина, Н.С., et al.. (1996). HB Sögn or α₂β₂14(A11)LEU → ARG in Combination with an α-Thalassemia Heterozygosity. Hemoglobin. 20(2). 131–134.

Сметанина, Н.С., et al.. (1996). 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. 20(3). 199–212. 4 indexed citations

Gu, L-H., et al.. (1995). Hb S-Hb Lufkin Dise in A Black Male Infant. Hemoglobin. 19(5). 291–294. 5 indexed citations

Gu, L-H., C. Öner, & T. H. J. Huisman. (1995). 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. 19(6). 413–418. 6 indexed citations

Molchanova, T. P., et al.. (1994). Hb Fannin-Lubbock in Five Spanish Families is Characterized by two Mutations: β111 GTC->CTC (VAL->LEU) AND β119 GGC->GAC (GLY->ASP). Hemoglobin. 18(4-5). 297–306. 7 indexed citations

Wilson, J. B., et al.. (1994). 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. 18(4-5). 343–345. 4 indexed citations

Baysal, E., et al.. (1994). Thalassemia intermedia in two patients with Hb lepore-β°-thalassemia (Frameshift codon 8, -AA). Hemoglobin. 18(3). 247–250. 3 indexed citations

10.

Huisman, T. H. J., et al.. (1993). Black α-Thalassemia-1: Partial Characterization of an ∼80 KB Deletion Which Includes the ξ- and α-Globin Genes. Hemoglobin. 17(4). 345–353. 3 indexed citations

11.

Molchanova, T. P., et al.. (1993). HB F-Sacromonte or α₂G_γ259(E3)LYS→GLN Observed in a Spanish Newborn and His Mother. Hemoglobin. 17(3). 269–274. 7 indexed citations

12.

Gu, L-H., J. B. Wilson, T. P. Molchanova, et al.. (1993). Three Sickle Cell Anemia Patients Each with a Different α Chain Variant. Diagnostic Complications. Hemoglobin. 17(4). 295–301. 1 indexed citations

13.

Gu, L-H., et al.. (1993). HB Tigraye OR α₂β²79(EF3)ASP→HIS(GAC→CAC): A Hemoglobin Variant with Increased Oxygen Affinity Observed in an Ethiopian Male. Hemoglobin. 17(3). 247–250. 7 indexed citations

14.

Molchanova, T. P., et al.. (1993). HB Madrid or α₂β₂115(G17)ALA→PRO in a Black Teenager. Hemoglobin. 17(3). 251–254. 5 indexed citations

15.

George, Elizabeth, A. L. Reese, E. Baysal, et al.. (1992). Types of Thalassemia Among Patients Attending a Large University Clinic in Kuala Lumpur, Malaysia. Hemoglobin. 16(1-2). 51–66. 42 indexed citations

16.

Molchanova, T. P., J. B. Wilson, L-H. Gu, et al.. (1992). A Second Observation of the Fetal Methehoglobin Variant HB F-M-Fort Ripley or α₂^Gγ₂⁹²(F8)HIS→TYR. Hemoglobin. 16(5). 389–398. 18 indexed citations

17.

Webber, B. B., J. B. Wilson, L-H. Gu, & T. H. J. Huisman. (1992). HB Ethiopia or α₂140(HC2)TYR→HISβ₂. Hemoglobin. 16(5). 441–443. 3 indexed citations

18.

Molchanova, T. P., J. B. Wilson, L-H. Gu, et al.. (1992). Hb Bab-Saaooun or α₂β₂48(CD7)Leu→pro, A Mildly Unstable Variant Found in an Arabian Boy from Tunisia. Hemoglobin. 16(4). 267–273. 11 indexed citations

19.

Huisman, T. H. J., F. Kutlar, & L-H. Gu. (1991). γ Chain Abnormalities and γ-Globin Gene Rearrangements in Newborn Babies of Various Populations. Hemoglobin. 15(5). 349–379. 21 indexed citations

20.

Plaseska‐Karanfilska, Dijana, J. B. Wilson, L-H. Gu, et al.. (1990). Hb Zengcg or α2β₂114(G16)Leu → Met. Hemoglobin. 14(5). 555–557. 6 indexed citations

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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