G. Flatz

2.7k total citations
112 papers, 2.2k citations indexed

About

G. Flatz is a scholar working on Genetics, Genetics and Hematology. According to data from OpenAlex, G. Flatz has authored 112 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Genetics, 39 papers in Genetics and 37 papers in Hematology. Recurrent topics in G. Flatz's work include Hemoglobinopathies and Related Disorders (39 papers), Digestive system and related health (35 papers) and Iron Metabolism and Disorders (23 papers). G. Flatz is often cited by papers focused on Hemoglobinopathies and Related Disorders (39 papers), Digestive system and related health (35 papers) and Iron Metabolism and Disorders (23 papers). G. Flatz collaborates with scholars based in Germany, Thailand and India. G. Flatz's co-authors include Torpong Sanguansermsri, Sibylle D. Flatz, J. Hundrieser, H. W. Rotthauwe, M. R. Chakravartti, H. Lehmann, John V. Kilmartin, A. Gropp, Ranjan Deka and Mahmud Ahmad and has published in prestigious journals such as Nature, The Lancet and American Journal of Clinical Nutrition.

In The Last Decade

G. Flatz

111 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
G. Flatz Germany	25	954	741	575	320	319	112	2.2k
R Lisker Mexico	26	813 0.9×	260 0.4×	296 0.5×	264 0.8×	278 0.9×	183	2.6k
E.R. Giblett United States	24	409 0.4×	522 0.7×	980 1.7×	450 1.4×	213 0.7×	53	2.4k
James G. Wilson United States	23	418 0.4×	159 0.2×	254 0.4×	292 0.9×	121 0.4×	49	1.8k
Donald L. Rucknagel United States	28	181 0.2×	1.3k 1.7×	904 1.6×	457 1.4×	452 1.4×	86	2.0k
Carmencita D. Padilla Philippines	22	596 0.6×	371 0.5×	141 0.2×	165 0.5×	962 3.0×	115	2.2k
Scott N. Swisher United States	18	138 0.1×	204 0.3×	494 0.9×	492 1.5×	129 0.4×	59	1.3k
Harold M. Nitowsky United States	28	701 0.7×	84 0.1×	139 0.2×	367 1.1×	893 2.8×	82	2.8k
Yuichi Akiyama Japan	25	443 0.5×	182 0.2×	507 0.9×	59 0.2×	126 0.4×	79	2.0k
Neil A. Hanchard United States	20	354 0.4×	255 0.3×	242 0.4×	145 0.5×	125 0.4×	54	1.2k
Sonja Pavlović Serbia	23	257 0.3×	344 0.5×	371 0.6×	88 0.3×	155 0.5×	180	1.9k

Countries citing papers authored by G. Flatz

Since Specialization

Citations

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

Fields of papers citing papers by G. Flatz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Flatz

This figure shows the co-authorship network connecting the top 25 collaborators of G. Flatz. A scholar is included among the top collaborators of G. Flatz 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 G. Flatz. G. Flatz 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

Sanguansermsri, Torpong, et al.. (2005). High Frequency of α-Thalassemia in the So Ethnic Group of South Laos. Acta Haematologica. 114(3). 164–166. 12 indexed citations

Flatz, G., et al.. (2004). The ‘Hot Spot’ of Hb E [β26(B8)Glu→Lys] in Southeast Asia: β‐Globin Anomalies in the Lao Theung Population of Southern Laos. Hemoglobin. 28(3). 197–204. 18 indexed citations

Sanguansermsri, Torpong, Heinrich Steger, Theera Tongsong, et al.. (2001). PRENATAL DIAGNOSIS OF β-THALASSEMIA MAJOR BY HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY ANALYSIS OF HEMOGLOBINS IN FETAL BLOOD SAMPLES. Hemoglobin. 25(1). 19–27. 20 indexed citations

Eigel, A., et al.. (1996). Prevalence of α-thalassemias in northern Thailand. Human Genetics. 98(3). 345–347. 72 indexed citations

Hundrieser, J., et al.. (1990). Study of Alpha-Thalassemia in Northeastern Thailand at the DNA Level. Human Heredity. 40(2). 85–88. 9 indexed citations

Yongvanit, Puangrat, Pote Sriboonlue, J. Hundrieser, et al.. (1989). DNA haplotypes and frameworks linked to the ?-globin locus in an Austro-Asiatic population with a high prevalence of hemoglobin E. Human Genetics. 83(2). 171–174. 19 indexed citations

Hundrieser, J., Torpong Sanguansermsri, Tamás Papp, & G. Flatz. (1988). Alpha-Thalassemia in Northern Thailand. Human Heredity. 38(4). 211–215. 15 indexed citations

Ahmad, Mahmud & G. Flatz. (1984). Prevalence of Primary Adult Lactose Malabsorption in Pakistan. Human Heredity. 34(2). 69–75. 12 indexed citations

Czeizel, Andrew E., G. Flatz, & Sibylle D. Flatz. (1983). Prevalence of primary adult lactose malabsorption in Hungary. Human Genetics. 64(4). 398–401. 14 indexed citations

10.

Hussein, Laila, et al.. (1982). Distribution of Human Adult Lactase Phenotypes in Egypt. Human Heredity. 32(2). 94–99. 12 indexed citations

11.

Flatz, G., et al.. (1982). Effect of acetylsalicylic acid on symptoms and hydrogen excretion in the disaccharide tolerance test with lactose or lactulose. American Journal of Clinical Nutrition. 35(2). 273–276. 12 indexed citations

12.

Benkmann, H.‐G., et al.. (1980). Properdin Factor B Polymorphism in Afghanistan. Human Heredity. 30(1). 39–43. 5 indexed citations

13.

Goedde, H. W., et al.. (1977). The Acetylator Polymorphism in four Populations of Afghanistan. Human Heredity. 27(5). 383–388. 8 indexed citations

14.

Flatz, G., et al.. (1973). Combined Erythrocyte Phosphohexose Isomerase and Glucose-6-Phosphate Dehydrogenase Deficiency. Human Heredity. 23(1). 83–87. 8 indexed citations

15.

Agarwal, D. P., et al.. (1973). A Note on Atypical Serum Cholinesterase and Genetic Factors in Leprosy. Human Heredity. 23(4). 370–373. 9 indexed citations

16.

Goedde, H. W., et al.. (1972). Genetic Survey in the Population of Assam II.. Human Heredity. 22(4). 331–337. 24 indexed citations

17.

Flatz, G., et al.. (1972). Genetic Survey in the Population of Assam I.. Human Heredity. 22(4). 323–330. 57 indexed citations

18.

Flatz, G., et al.. (1964). GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND JAUNDICE IN NEWBORN INFANTS IN NORTHERN THAILAND.. PubMed. 203. 39–45. 6 indexed citations

19.

Flatz, G., et al.. (1963). Negative Balancing Factors for the Glucose-6-Phosphate Dehydrogenase Polymorphism in Thailand. Human Heredity. 13(4). 316–327. 1 indexed citations

20.

Flatz, G., et al.. (1963). MALARIA AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN THAILAND. The Lancet. 282(7320). 1248–1250. 20 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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